METHODS OF PRESCREENING AND TREATING BREAST CANCERS WITH SELECTIVE ANDROGEN RECEPTOR MODULATORS

FIELD OF INVENTION

[0001] This invention relates to methods of prescreening candidates for selective androgen receptor modulator (SARM) therapy and methods of treatment of breast cancers with selective androgen receptor modulators (SARMs). The invention further provides methods of: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of estrogen receptor (ER), progesterone receptor (PR), and/or human epidermal growth factor receptor 2 (HER2); i) prescreening then treating a subject suffering from triple negative breast cancer (TNBC); j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening, treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prolonging survival of a subject with breast cancer; o) slowing the progression of breast cancer in a subject; p) prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2-positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer; the methods comprise administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound of Formulae I-XIV as described herein.

BACKGROUND OF THE INVENTION

[0002] Breast cancer is a disease that kills over 45,000 women each year in the United States alone. Over 180,000 new cases of breast cancer are diagnosed annually, and it is estimated that one in eight women will develop breast cancer. These numbers indicate that breast cancer is one of the most dangerous diseases facing women today. Breast cancer occurs in men as well, but at a much lower incidence. Cancer research has been unable to determine the cause of breast cancer and has not found a suitable method of therapy or prevention. [0003] Genotyping has long been used to screen women who may be genetically predisposed to developing breast cancer. It is another diagnostic or prognostic tool that can be used to determine the availability of therapies. Certain women are predisposed to develop breast cancer based on the presence of germline (i.e., inherited) mutations in the breast cancer susceptibility genes ( BRCA ) type 1 ( BRCA1 ) or BRCA2. A couple of SERMs, tamoxifen in 1999 and raloxifene in 2007, were approved for the primary prevention of breast cancer in patient populations that are high risk based on family history and/or genotype considerations. However, hysterectomy or prophylactic mastectomy was often considered in these patients as a more definite preventative. In 2018 and 2019, talazoparib (Talzenna) and olaparib (Lynparza), inhibitors of the enzyme poly ADP ribose polymerase (PARP), were approved for metastatic ER-positive and HER2-negative breast cancer patients with certain inherited BRCA mutations who have received chemotherapy (and hormone therapy if ER-positive). In 2019, alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase (PI3K) with inhibitory activity predominantly against PI3Ka was approved for patients possessing certain gain-of-function mutations in the gene encoding the catalytic a-subunit of PI3K (PIK3CA). These mutations lead to activation of PI3Ka and Akt-signaling, cellular transformation and the generation of tumors in in vitro and in vivo models. PI3K inhibition by alpelisib treatment has been shown to induce an increase in estrogen receptor (ER) transcription in breast cancer cells. The combination of alpelisib and fulvestrant demonstrated increased antitumor activity compared to either treatment alone in xenograft models derived from ER-positive, PIK3CA mutated breast cancer cell lines. PIK3CA mutations are present in about 30-40% of breast cancer tumors and most prevalent in ER-positive patients.

[0004] The standard of care currently includes screening the tumor for the expression levels of the hormone receptors, estrogen receptor (ER) and progesterone receptor (PR), and the human epidermal growth factor receptor 2 (HER2) kinase. Currently, a woman diagnosed with breast cancer may be treated preliminarily with surgery, chemotherapy (optional in some cases), and radiation before targeted therapy is initiated. Hormone receptor-positive breast cancers are susceptible to hormone therapies (also referred to as endocrine therapies) with selective estrogen receptor modulators or SERMs (e.g., tamoxifen, toremifene, raloxifene), aromatase inhibitors or AI’s (e.g., anastrozole, letrozole, exemestane), or selective estrogen receptor degraders or SERDs (e.g., fulvestrant). Hormone therapies such as gonadotropin-releasing hormone (GnRH) agonists (typically used in pre- and peri-menopausal women) and aromatase inhibitors (AI) (typically used in post-menopausal women or together with GnRH agonists in pre- or peri-menopausal women) block production of estrogens in the body, whereas SERMs and SERDs block the proliferative action of estrogens on the breast cancer cells. While the prognosis of most early-stage ER-positive breast cancer patients is relatively good compared to non-hormonal cancers, adjuvant hormone therapy failures do occur resulting in recurrence, including distant metastases (i.e, advanced breast cancer). Metastatic or advanced breast cancer, whether hormone naive or progressive despite endocrine therapy, is often still ER- positive and still dependent on the ER axis for growth. The treatment of advanced breast cancer is rapidly evolving from the use of an endocrine monotherapy such as SERM or AI or fulvestrant, to combinations of an endocrine therapy with recently approved kinase inhibitors, including the cyclin-dependent kinase 4/6 (CDK 4/6) inhibitors (palbociclib (approved 2015), ribociclib (approved 2017), or abemaciclib (approved 2017), trilaciclib, lerociclib), or mechanistic target of rapamycin (mTOR) inhibitor (everolimus (approved 2012)). These combination therapies delay progression of advanced breast cancer compared to endocrine therapy alone and are supplanting the use of endocrine therapy alone in late breast cancer.

[0005] Certain common mutations of the estrogen receptor alpha can be treatment emergent and confer resistance to the approved endocrine therapies even when combined with various kinase therapies as discussed above. It has been discovered that at least one mutation (e.g., Y537S) described herein which despite SERM, AI, and fulvestrant resistance is still sensitive to the androgen agonists of this invention. Consequently, even late-stage ER-positive AR- positive breast cancer patients which have been exposed to the full endocrine- and directed- therapy milieu may still have further hormonal treatment options before being relegated to chemotherapies. If screening reveals certain ER mutants then their treatment can be personalized to include the use of SARMs to delay progression of the disease and/or regress tumors.

[0006] HER2-positive breast cancers are susceptible to HER2 kinase inhibitors (e.g., trastuzumab, lapatinib, neratinib, and tucatinib) and are generally used in metastatic disease. Anti-angiogenic therapy (bevacizumab) was also approved in metastatic disease, but the FDA removed this for bevacizumab in 2011. Despite these multiple tiers of targeted treatments, patients often have or develop refractory forms of breast cancer. Examples of refractory breast cancer include primary tumors which are triple-negative (lacking ER, PR, HER2), hormone resistant (SERM-, SERD-, or AI-resistant), or kinase inhibitor resistant (e.g., inhibitors of CDK 4/6, mTor, and/or HER2), or metastatic breast cancer tumors. Once all the targeted therapies fail e.g., metastatic tumors are re-activated or tumors further metastasize, radiation and high dose chemotherapy are required to ablate the refractory breast cancer tumors. Current chemotherapies available for the treatment of refractory breast cancer include anthracy clines, taxanes, and epothilones, which are toxic, dangerous, costly, intravenous, and often are ineffective, especially in the treatment of metastatic disease.

[0007] Abundant clinical evidence suggests that androgens normally inhibit breast growth. For instance, women with androgen deficits have an increased risk for developing breast cancer. Androgen signaling plays a crucial role in breast homeostasis, negating the proliferative effects of estrogen signaling in the breast. However, when steroidal androgens biotransform into estrogens (via aromatase pathway), they increase cell proliferation and mammary carcinogenesis risk. Historically, the steroidal androgen receptor agonists testosterone, fluoxymesterone, and calusterone were used in advanced breast cancer. These agents suffered from side effects such as excessive virilization, cross-reactivity with the estrogen receptor, and aromatization to estrogens. The use of steroidal androgens in advanced breast cancer pre-dates the screening of breast cancers for hormone and kinase receptors. Recently, it was found that the AR is expressed in 50-90% of breast tumors, providing a mechanism to use androgens as targeted therapy for AR-positive breast cancers.

[0008] Although the majority of breast cancers are considered hormone receptor-positive (ER, PR, or HER2), 15-20% of women diagnosed with breast cancer will have Triple Negative Breast Cancer (TNBC) which is characterized by a lack of expression of ER, PR, or HER2. TNBC occurs more frequently in younger patients (<50 years of age) and generally shows a more aggressive behavior. Until recently, those patients with advanced TNBC were limited to standard palliative treatment options such as cytotoxic chemotherapy.

[0009] Efficacy of chemotherapy was improved by the use of an antibody directed conjugate therapy, sacituzumab govitecan (Trodelvy), that delivers SN-38, which is the active metabolite of the topoisomerase inhibitor I irinotecan, to TNBC patients expressing Trop-2 (human trophoblast cell-surface antigen 2) on their breast cancer cells. Topoisomerases I and II are normal host enzymes that are found in the nucleus of mammalian cells and are required for normal DNA replication and cellular division. The enzymes create and then repair single stranded nicks in cellular DNA. The nicks allow for the untangling and relaxation of supercoiled double stranded DNA, so that replication can proceed. Once the DNA torsional strain has been relieved, the topoisomerase reseals the relaxed double helix. Topoisomerase activity is particularly increased in rapidly dividing and in cancer cells. If topoisomerase is inhibited, the accumulation of DNA breaks results in inhibition of DNA replication and cell death. It represents an appropriate, but nonselective target for anticancer therapy.

[00010] An experimental microtubule disruptor, sabizabulin |(2-( 1H-indol-3-yl)imidazol-4- yl)(3,4,5-trimethoxyphenyl)methanone and alternate resonance form (2-( 1H-indol-3- yl)imidazol-5-yl)(3,4,5-trimethoxyphenyl)methanone], has been demonstrated to bind to the colchicine binding site of tubulin and inhibit (CBSI) tubulin dynamics. These agents are orally active, and unlike colchicine, these CBSI’s are not substrates for efflux channels that pump anticancer agents from cancer cells and CBSI’s can overcome taxane-resistance. CBSI inhibition of tubulin dynamics causes apoptotic cell death due to arrest in G2/M phase of mitosis. Deng et al. have recently characterized sabizabulin in a variety of in vitro and in vivo models of TNBC and confirmed potent and high efficacy tumor growth inhibition in primary and metastatic tumors, and prevention of metastasis to distance organs including liver, lung, spleen, and brain in taxane-sensitive (MDA-MB-231) and taxane-resistant models of TNBC including patient-derived xenografts.

[00011] However, even after initial response to chemotherapy, the duration of the response may be short and there is a higher likelihood of visceral metastases, rapidly progressive disease, and inferior survival compared to hormone receptor positive breast cancer. Therefore, research is focused on identifying therapeutic targets in TNBC.

[00012] A novel approach to treating TNBC was approved in which antibodies blocking programmed death ligand 1 (PD-L1) were employed in PD-LI positive patients. One such antibody is atezolizumab (Tecentriq; approved for TNBC in 2019) and another is pembrolizumab (Keytruda; approved for TNBC in 2020). Median progression-free survival (PFS) of 7.4 months was observed in atezolizumab and nab-paclitaxel, compared with 4.8 months for those on placebo and nab-paclitaxel lead to approval of atezolizumab. For pembrolizumab, median PFS was 9.7 months in the pembrolizumab plus chemotherapy arm and 5.6 months in the placebo arm.

[00013] One hormone receptor target still available in ER-positive, HER2-positive and triple negative breast cancers is the androgen receptor (AR). The AR is the most highly expressed steroid receptor in breast cancer with up to 95% of ER-positive breast cancers expressing AR (see Example 9 infra). In TNBC, up to 30% of cancers may express AR. Historically, AR has been considered anti-proliferative and beneficial in hormone receptor positive breast cancers. In TNBC, data demonstrates that the presence of AR and androgen synthesizing enzymes is associated with lower proliferation, lower tumor grade, better overall survival, and more favorable clinical outcomes as compared to those patients with TNBC not expressing AR.

[00014] In overview, activation of the AR by selective androgen receptor modulators (SARMs) of this invention is believed to drive differentiation of TNBC cells away from an aggressive TNBC phenotype that acquires metastatic potential as a result of epitheliakmesenchymal stem cell (MSC) interaction. Either one of the two cell types alone lacks the capability to metastasize to distant organs. Invasion of other organs arises due to paracrine factors secreted during epithelial:MSC interaction. Although three factors, namely CCL5, IL6, and MMP13 are up-regulated during the interaction, in vitro and in vivo studies indicate that CCL5 is the key contributor to the metastatic characteristics of breast cancer. Other studies have also identified the role of IL6 in metastasis and trastustumab-resistance. These findings underscore the importance of these paracrine factors in breast cancer metastasis and abrogating these factors and subsequently epithelial:MSC interactions will prevent metastasis. Requiring a threshold level AR staining (e.g., >40%) as a prescreen for treating TNBC with a SARM maximizes the likelihood that AR would drive differentiation if activated in these TNBC patients. Evidence also suggests that the AR target gene prostate specific antigen (PSA) is a favorable prognostic marker in breast cancer (not just TNBC). Based on these findings, research is focused on AR as a potential therapeutic target.

[00015] Trodelvy plus Enobosarm (Formula IX)

[00016] TRODELVY® (sacituzumab govitecan-hziy) is a prescription medicine used to treat adults with triple-negative breast cancer (negative for estrogen and progesterone hormone receptors and HER2) that has spread to other parts of the body (metastatic) or cannot be removed by surgery, and who have received two or more prior treatments, including at least one treatment for metastatic disease. Trodelvy would be inhibiting topoisomerase I in the rapidly growing TNBC cells thereby causing accumulation of DNA breaks and resulting in inhibition of DNA replication and apoptotic cell death. Whereas the selective androgen receptor modulator (SARM) as described herein has activity in TNBC by acting through the AR which is the one steroid receptor that may still be active in TNBC. By selecting patients with an increased threshold of percent AR staining (e.g., >40%) it may be possible to drive a differentiation program for the TNBC cells away from the aggressive TNBC phenotype. Trodelvy combined with a SARM as described herein would be complementary because while one is causing cell death and the other driving differentiation away from the aggressive TNBC phenotype. The result could be additive or even synergistic efficacy in TNBC patients, particularly those with >40% AR staining.

[00017] Sabizabulin plus Enobosarm (Formula IX)

[00018] Sabizabulin is an oral, first-in-class alpha and beta tubulin inhibitor/cytoskeleton disruptor small molecule. It has shown in preclinical studies to have efficacy against many tumor types including castration resistant prostate cancer, triple negative breast cancer, ovarian cancer, cervical cancer, lung cancer, melanoma, leukemia, glioma, and pancreatic cancer. The selective androgen receptor modulator (SARM) as described herein has activity in TNBC by acting through the AR which is the one steroid receptor that may still be active. By selecting patients with an increased threshold of percent AR staining (e.g., >40%) it may be possible to drive a differentiation program for the TNBC cells away from the aggressive TNBC phenotype. Whereas sabizabulin would be impacting the microtubules and therefore inhibiting cell division of the rapidly growing TNBC cells causing apoptosis. Therefore, a SARM as described herein plus sabizabulin would be complementary with one driving differentiation away from the aggressive TNBC phenotype and the other inhibiting TNBC cell growth. The result could be additive or even synergistic efficacy in TNBC patients, particularly in patients with above threshold percent AR staining.

[00019] Prolonged treatment of cancers with estrogen synthesis inhibitors (AI or GnRH agonists) or ER antagonists (SERMs or SERDs) results in mutations in the target protein and activation of resistance pathways. For example, continued treatment of ER-positive breast cancers with ER antagonists or aromatase inhibitors (AI) results in resistance due to mutations in the ER ligand binding domain (LBD). Clinical studies have estimated that over 30% of breast cancers treated with tamoxifen become refractory and recur as a resistant cancer and over 40% of recurrent breast cancers express mutated ER. Treatment emergent mutant ERs have escaped inhibition of the hormonal axis fail to respond to endocrine therapy and, consequently, these patients will need to be treated with chemotherapeutic agents. Such cancers require new non- or less- toxic effective endocrine therapies. One possibility is the pharmacogenomic screening of tumors or circulating tumor cells for the present of mutant ERs that would confer resistance to current endocrine therapies. This could be done upon molecular phenotyping as ER-positive (i.e., early disease) or, alternatively, in patients that have failed endocrine therapies (i.e, late disease) such as SERM, AI, SERD and/or GnRH agonist whether or not combined with CDK 4/6 or mTor inhibitors. [00020] Selective androgen receptor modulators (SARMs) are compounds which demonstrate AR-mediated tissue selective activity. Unlike their steroidal precursors, SARMs are non- aromatizable, generally demonstrate no activity at other steroidal receptors including ER and PR, and are non- virilizing. Further, SARMs may be beneficial in refractory breast cancer patients due to their hypermyoanabolic effects that should improve their tolerance of high-dose chemotherapy. Further, SARMs have beneficial osteoblastic and anti-osteoclastic effects in bones that may decrease the risk of metastasis to the bones or may decrease risk of osteoporosis during endocrine and/or chemotherapies.

[00021] Immunohistochemical (IHC) staining has been used to report a tumor as ER-positive or AR-positive so long as there is any staining for the receptor of interest. For example, the cut-off value for ER-positivity was set at >1%, as suggested by American Society of Clinical Oncology Guideline Recommendations for immunohistochemical testing of estrogen and progesterone receptors in breast cancer and the same cut-off was also adopted for AR positivity.

[00022] New innovative approaches are urgently needed at both the basic science and clinical levels to develop methods for: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado- trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; and/or p) prescreening then prolonging progression- free survival of a subject with breast cancer; q) prescreening then treating, preventing, suppressing or inhibiting AR-positive triple negative breast cancer; r) prescreening then treating a subject suffering from HER2 -positive breast cancer; s) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or t) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer.

SUMMARY OF THE INVENTION

[00023] In one aspect, this invention provides a method of prescreening a breast cancer in a subject for whether said breast cancer is susceptible to selective androgen receptor modulator (SARM) treatment, comprising obtaining a biological sample from said subject prior to said SARM treatment and analyzing for whether said sample has an androgen receptor (AR)- positive staining. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 35%. In other embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 70%.

[00024] In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 40%, or 50%, or 60%, or 70%, or 80%.

[00025] In one aspect, the invention provides a method of prescreening a breast cancer in a subject for whether said breast cancer is susceptible to selective androgen receptor modulator (SARM) treatment, comprising obtaining a biological sample from said subject prior to said SARM treatment and analyzing for whether said sample has a percent androgen receptor (AR)- positive staining above a threshold value. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 35%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%.

[00026] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 2% to 100%, or from 5% to 100%, or from 10% to 100%, or from 15% to about 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 55% to 100%, or from 60% to 100%, or from 65% to 100%, or from 70% to 100%.

[00027] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 10% to 100%, or from 15% to 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 60% to 100%, or from 70% to 100%.

[00028] In one aspect, the invention provides a method for treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM), comprising analyzing a biological sample obtained from said subject prior to treatment to determine whether said sample has an androgen receptor (AR)-positive staining and administering to said subject a therapeutically effective amount of the selective androgen receptor modulator (SARM). In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 35%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%.

[00029] In one aspect, the invention provides a method of treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM), comprising analyzing a biological sample obtained from said subject prior to treatment to determine whether said sample has a percent androgen receptor (AR)-positive staining above a threshold value then administering to said subject a therapeutically effective amount of the selective androgen receptor modulator (SARM). In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 35%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%.

[00030] In some embodiments of the method of the invention, e.g., the method of prescreening a breast cancer of the invention then treating said breast cancer of the invention, the SARM compound is represented by a structure of formula I:

I wherein

X is a bond, O, CH ₂ , NH, S, Se, PR, NO, or NR;

G is O or S; T is OH, OR, -NHCOCH3, or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF3, CF ₂ CF3, aryl, phenyl, halogen, alkenyl, or OH;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ; R ₂ is H, F, Cl, Br, I, CH ₃ , CF ₃ , OH, CN, N0 ₂ , NHCOCTH, NHCOCF ₃ , NHCOR, alkyl, arylalkyl, OR, NH ₂ , NHR, N(R) ₂ , or SR;

R ₃ is H, F, Cl, Br, I, CN, N0 ₂ , COR, COOH, CONHR, CF ₃ , Sn(R) ₃ , or R ₃ together with the benzene ring to which it is attached forms a fused ring system represented by the structure:

Z is N0 ₂ , CN, COR, COOH, or CONHR;

Y is CF ₃ , F, Br, Cl, I, CN, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR,

COR, OCOR, 0S0 ₂ R, S0 ₂ R, or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C: n is an integer of 1-4; and m is an integer of 1-3, or an optical isomer, a racemic mixture, a pharmaceutically acceptable salt, a pharmaceutical product, a hydrate, an Y- oxide, or a crystal thereof.

[00031] In some embodiments of the method of the invention, the SARM compound is represented by a structure of formula VIII, IX, X, XI, XII, XIII, or XIV :

XIV. [00032] In some embodiments of the method of the invention, the SARM compound is represented by a structure of formula IX:

IX. [00033] In another aspect, the invention provides a method for treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM), comprising analyzing a biological sample obtained from said subject prior to treatment to determine whether said sample has an androgen receptor (AR)-positive staining of greater than or equal to 40% and administering to said subject the selective androgen receptor modulator (SARM), wherein said SARM compound is represented by the structure of formula IX

IX.

[00034] In some embodiments of the method of the invention, the breast cancer is an AR- positive breast cancer, ER-positive breast cancer, triple negative breast cancer, HER2 -positive breast cancer, advanced breast cancer, refractory breast cancer, metastatic breast cancer, or breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof. In some embodiments, the breast cancer is AR-positive metastatic breast cancer. In some embodiments, the breast cancer is AR-positive and ER-positive breast cancer.

BRIEF DESCRIPTION OF THE DRAWINGS

[00035] The subject matter regarded as the invention is particularly pointed out and distinctly claimed in the concluding portion of the specification. The invention, however, both as to organization and method of operation, together with objects, features, and advantages thereof, may best be understood by reference to the following detailed description when read with the accompanying drawings in which:

[00036] Figure lA-Figure 1J illustrate that DHT and a compound of Formula IX inhibit MDA-MB-231 triple negative breast cancer cell growth. Figure 1A shows MDA-MB-231 cell expression of AR following transfection. Figure IB shows the IC50 in AR-positive MDA-MB- 231 cells. Figure 1C- Figure 1J show the effects of DHT, Formula IX, bicalutamide and the (R) enantiomer of Formula IX on percent (%) cell survival. (Figure 1C, Figure IE, Figure 1G and Figure II cells were treated in charcoal stripped FBS. Figure ID, Figure IF, Figure 1H and Figure 1J cells were treated in full serum). · MDA-MB-231 with lacZ; o MDA-MB-231 with AR 200 μL; ▲ MDA-MB-231 with AR 500 pF.

[00037] Figure 2A -Figure 2H illustrate that DHT and Formula IX inhibit HCC-38 triple negative breast cancer cell growth. Figure 2A shows HCC-38 cell expression of AR following transfection. Figure 2B shows the IC50 in AR-positive HCC-38 cells. Figure 2A-Figure 2H show the effects of DHT, Formula IX and Bicalutamide on percent (%) cell survival. (Figure 2C, Figure 2E and Figure 2G cells were treated in charcoal stripped FBS. Figure 2D, Figure 2F and Figure 2H cells were treated in full serum). · HCC-38 with lacZ; o HCC-38 with AR 200 pF; ▲ HCC-38 with AR 500 pF. [00038] Figure 3A-Figure 3E illustrate that the effect of DHT and Formula IX on MDA-MB- 231 cells was reversed by bicalutamide. Figure 3A-Figure 3D show the effects of DHT or Formula IX in the presence or absence of bicalutamide, on percent (%) cell survival. (Figure 3 A and Figure 3C cells were treated in charcoal stripped FBS. Figure 3B and Figure 3D cells were treated in full serum). · lacZ and with 10 mM bicalutamide; o lacZ; ▲ AR with 10 mM bicalutamide; D AR. Figure 3E shows IC ₅₀ values in AR-positive cells in the presence or absence of pretreatment with bicalutamide.

[00039] Figure 4A-Figure 4Q illustrate that AR agonists inhibit triple negative breast cancer cell growth. Figure 4A, Figure 4B, Figure 4E, Figure 4F, Figure 4G, Figure 4H, Figure 4K, Figure 4L, Figure 4M, Figure 4N, Figure 40 and Figure 4P show effect of AR agonists on percent (%) cell survival. Figure 4C and Figure 4D show the effect of AR antagonist on percent (%) cell survival. Figure 41 and Figure 4J show the effect of AR non-binder on percent (%) cell survival. Figure 4A, Figure 4C, Figure 4E, Figure 4G, Figure 41, Figure 4M and Figure 40 cells were treated in charcoal stripped FBS. Figure 4B, Figure 4D, Figure 4F, Figure 4H, Figure 4J, Figure 4L, Figure 4N and Figure 4P cells were treated in full serum. Figure 4Q shows EC50 and IC50 values in AR-positive cells.

[00040] Figure 5 illustrates that growth inhibitory ligands are AR agonists in MDA-MB-231 cells.

[00041] Figure 6A-Figure 6E illustrate that growth inhibitory effects in MDA-MB-231 cells are selective to AR. Figure 6A and Figure 6B show the expression of ERa or ERP in MDA- MB-231 cells following transfection, respectively. Figure 6C, Figure 6D and Figure 6E show the effects of estradiol (E2) or ICI 182,780 (ICI) on percent (%) cell survival. (Figure 6C cells were treated in charcoal stripped serum. Figure 6D and Figure 6E cells were treated in full serum).

[00042] Figure 7 shows DHT alters the morphology of MDA-MB-231 cells.

[00043] Figure 8 illustrates the effect of Formula VIII on steroid receptor transactivation (agonist mode).

[00044] Figure 9 depicts a dose response curve of PR activity (antagonist mode) for compound of Formula VIII, Formula IX, R-enantiomer of Formula IX and RU486. The closed circles (·) correspond to Formula VIII data points (IC50 = 17.05 nM); open circles (o) correspond to Formula IX (IC50 = 162.9 nM); closed triangles (▼) correspond to R-enantiomer of Formula IX (IC50 = 1689 nM); and open triangles (D) correspond to RU486 (IC50 = 0.048 nM).

[00045] Figure 10A-Figure 10B demonstrate that SARM (Formula VIII) inhibits MDA-MB- 231-AR tumor growth. Body weight (10A) and tumor size (10B) were measured for 35 days in intact female nude mice having 150-200 mm ³ tumors from MDA-MB-231-AR triple negative breast cancer cells and then orally administered vehicle (*) or 30 mg/kg of Formula VIII (·).

[00046] Figure 11 demonstrates that SARM (Formula VIII) inhibits MDA-MB-231-AR tumor growth. Tumor size in mm ³ (left pane) and % change in tumor size (middle pane), as well as tumor weight (right pane) were measured after 35 days in intact female nude mice having 150-200 mm ³ tumors from MDA-MB-231-AR triple negative breast cancer cells and then receiving oral administration of vehicle or 30 mg/kg of Formula VIII.

[00047] Figure 12 demonstrates the morphology of MDA-MB-231 breast cancer cells stably transfected with AR (MDA-MB-231-AR cells). The results indicate that AR agonists, DHT, Formula IX, and Formula VIII altered the morphology into a more anchored phenotype compared to vehicle, bicalutamide or an inactive isomer of Formula IX. This may be indicative of a less metastatic breast cancer phenotype.

[00048] Figure 13A-Figure 13C demonstrate binding and transactivation of the indicated ligands to HEK-293 (13A) or MDA-MB-231 (13B & 13C) cells. DHT, Formula IX and Formula VIII are agonists of AR in breast cancer cells. (Example 16)

[00049] Figure 14 demonstrates anti-proliferative activity of DHT and SARMs in MDA-MB- 231 breast cancer cells stably transfected with AR. MDA-MB-231 cells stably transfected with AR using lentivirus were treated with the indicated ligands for 6 days and the number of cells counted using Coulter counter. DHT and SARMs (VIII and IX), but not the AR antagonist, bicalutamide, inhibited the proliferation of MDA-MB-231 triple negative breast cancer cells stably transfected with AR.

[00050] Figure 15 presents microarray results showing that activated AR (AR activated by compound of Formula VIII) suppressed the expression of more genes than it induced in MDA- MB-231-AR xenograft breast cancer cells.

[00051] Figure 16 depicts validation of microarray results.

[00052] Figure 17 illustrates that Formula VIII inhibited the growth of MCF-7-AR triple positive xenograft. [00053] Figure 18 presents inhibition of uterus weight gain in estrogen supplemented animals treated with Formula VIII, demonstrating the ability of a SARM to counteract estrogenic stimuli in vivo.

[00054] Figure 19 shows that the AR expression pattern in response to an AR- agonist (Formula VIII) is similar to that observed in prostate cancer cells.

[00055] Figure 20 depicts validation of microarray results.

[00056] Figure 21 demonstrates up-regulation of JNK phosphorylation in MCF7-AR tumors using Formula VIII.

[00057] Figure 22 shows inhibition of triple negative breast cancer (TNBC) growth using Formulae VIII and IX. Formula VIII and Formula IX demonstrated -85% TGI at all doses tried (5, 10 mg per kg for Formula VIII; 5, 10, 30 mg per kg for Formula IX) in the TNBC model using MDA-MB-231-AR cells in nude mice.

[00058] Figure 23 demonstrates inhibition of triple negative breast cancer using Formulae VIII and IX. The tumor weights were likewise reduced for all doses of Formula VIII and Formula IX. Spleen enlargement (680 mg vs. 200-300 mg for normal mice) was seen only in vehicle treated mice, possibly indicative of prevention by the SARMs of tumor metastasis to the spleen.

[00059] Figure 24 shows increased body weight by the SARMs at all doses of Formula VIII and Formula IX, indicative of healthy growth and a lack of toxicity. By comparison, the vehicle treated animals did not grow as robustly.

[00060] Figure 25A - Figure 25E depict antagonism by SARM regarding the ability of estradiol to activate ER target genes in MCF-7-AR cells. Figure 25B and Figure 25D show that adding AR (as opposed to Green Fluorescent Protein (GFP) as seen in Figures 25A and 25C) to MCF-7-AR cells increases the effects of estradiol (when unopposed) on the ER target genes PR and PS2, respectively. Adding AR to MCF-7-AR cells suppressed the activation of these ER targets in the presence of SARM alone or SARM + estradiol (E2) as compared to GFP transfected cells (i.e., no AR; Figure 25A and Figure 25C). Figure 25E shows that AR target genes are enhanced by SARM even in the presence of estradiol.

[00061] Figure 26A and Figure 26B depict immunohistochemistry of two regions of the same BR-0001 tumor, a triple negative breast cancer (TNBC). They show that AR expression is consistent throughout this formalin-fixed, paraffin-embedded (FFPE) tissue stained with AR antibody (AR N20 from SCBT). Figure 26C depicts immunohistochemistry staining of an AR- negative TNBC FFPE tumor as a negative control.

[00062] Figure 27A-Figure 27C depict BR-0001 tumor xenograft growth inhibition by Formula IX compared to enzalutamide (Enza) or vehicle in terms of breast cancer tumor volume (Figure 27 A and Figure 27B) and weight (Figure 27 C) with time. Experiments 1 and 2 were duplicate experiments ran at different times with n=5 and n=10 animals, respectively. Figure 27A provides results for Experiment 1, Figure 27B provides results for Experiment 2 and Figure 27C provides results for Experiment 2. BR-0001 TNBC fragments of 1 mm ³ (approximately) were implanted subcutaneously in NOD scid gamma (NSG) mice. Once the tumors reach 100- 200 mm ³ , the animals were randomized and treated with vehicle, 10 mg/kg/day Formula IX or enzalutamide orally. Tumor volume was measured thrice weekly. Animals were sacrificed and tumors were weighed.

[00063] Figure 28A-Figure 28B depict immunohistochemistry of BR-0001 tumors from animals treated with vehicle or Formula IX and stained for Ki-67. Ki-67 was reduced in tumors of animals treated with Formula IX. Quantification of Ki-67 indicated an approximately 50% reduction in Ki-67 staining in 2 weeks of treatment. Tumors from experiment 2 were fixed in formalin and paraffin embedded. Slides were cut and stained with Ki-67 antibody (Figure 28A), Ki-67 staining was reduced in tumors of animals treated with Formula IX. Ki-67 positive cells in each slide (total of 200 cells per view) were counted and represented as % stained cells (Figure 28B). As a reference, inset into the graphics are bars which are 200 microns (μm) in length.

[00064] Figure 29 depicts Z-scores of 50 genes (PAM50) used to identify BR-0001. PAM50 is a set of 50 genes used to classify breast cancers. PAM50 gene expression data indicated that the BR-0001 tumor belonged to basal-like breast cancer (BLBC) subtype of TNBC. The expression (Z-score) of 50 genes required to classify the breast cancer is given here.

[00065] Figure 30A and Figure 30B depict gene expression data which is compared to the genes published (Pietenpol group) as useful to classify the Basal-Like Breast Cancer (BLBC) into subclassification. Sub-classification indicated that BR-0001 belonged to luminal androgen receptor (LAR) and mesenchymal stem-like (MSL) subtypes. The six TNBC subtypes according to the Pietenpol group include two basal-like (BL1 and BL2), an immunomodulatory (IM), a mesenchymal (M), a mesenchymal stem-like (MSL), and a luminal androgen receptor (LAR) subtype. GE - gene expression.

[00066] Figure 31 depicts gene expression changes in BR-0001 tumors treated with Formula IX.

[00067] Figure 32 depicts reduced tumor growth of ER-positive, PR-positive, HER2-positive and AR-positive tumors composed of HCI-007 cells using Formula IX.

[00068] Figure 33A and Figure 33B depict potent tumor growth reduction using Formula IX in xenografts composed of HCI-013 cells. HCI-013 phenotype is a triple positive and also expresses AR. Figure 33 A: tumor volume changes (%) and Figure 33B: tumor weight (g).

[00069] Figure 34A -Figure 34E depict that AR agonists inhibited proliferation of ER- and AR- positive breast cancer cells. Figure 34A depicts that Formula IX inhibited the proliferation of ZR-75-1 cells. ZR-75-1 breast cancer cells plated in growth medium (n=4/treatment) were treated with indicated doses of Formula IX for 6 days, with medium changed and re-treated on day 3. After 6 days of treatment, cells were harvested, and the number of cells was counted. Figure 34B depicts that Formula IX inhibited proliferation of MCF-7 cells expressing AR. MCF-7 cells stably transfected with GFP (MCF-7-GFP) or the AR (MCF-7-AR) were plated in 96 well plates in growth medium (n=4/treatment) and treated with the indicated doses of Formula IX. Medium was changed after 3 days and re-treated. Cells were fixed after 6 days of treatment and the cell viability was measured by SRB assay. Figure 34C depicts that breast cancer fibroblasts treated with AR agonists secreted factors that inhibited MCF-7-GFP cells lacking supplemented AR. Primary fibroblasts obtained from a breast cancer patient were cultured in growth medium and were treated in triplicates with vehicle, 10 nM DHT, 1 mM enzalutamide, or 1 pM Formula IX. Medium was changed, and the cells were re-treated on days 4 and 7. Medium was collected, pooled from triplicates, and stored in -80°C. After 10 days of treatment, cells were fixed, and cell viability was measured using SRB. MCF-7 cells stably transfected with GFP (MCF-7-GFP) were plated in growth medium. Twenty-four hours after plating, cells were fed with the conditioned medium obtained from patient-derived fibroblasts as indicated above. Cells were fed for 10 days with conditioned medium, with medium changed on days 4 and 7. After 10 days of treatment, cells were fixed, and the viability was measured by SRB assay. Figure 34D depicts that AR ligands did not inhibit growth of ER-negative AR- positive HCI-9 PDX. AR-positive, but ER-negative HCI-9 PDX was surgically implanted as 1 mm ³ fragments under the mammary fat pad in NSG mice (n=8- 10/group). Once the tumors reached 100-200 mm ³ , the mice were randomized and treated with vehicle (DMSO:PEG-300 (15%:85%)), Formula IX (10 mpk p.o.), or enzalutamide (30 mpk p.o.). Tumor volume was measured thrice weekly. Figure 34E depicts that HCI-13 ER-a was resistant to ER antagonists fulvestrant and tamoxifen (right pane) compared to wt-ER-oc (left pane). ER-a from HCI-13 was cloned into pCR3.1 vector. Wildtype ER-a and HCI-13 ER-a, ERE-LUC, and CMV-LUC were transfected into COS-1 cells using lipofectamine. Cells were treated 24 hours after transfection with vehicle, 0.1 nM estradiol, 10 nM fulvestrant or 1 mM tamoxifen in combination with 0.1 nM estradiol. Twenty four hours after treatment cells were harvested and luciferase assay was performed. ER antagonists in wt-ER-oc were significantly different than vehicle-treated wt-ER-oc as depicted by * p<0.05. AR-androgen receptor; GFP-green fluorescent protein; DHT-5oc-dihydrotestosterone; E2- 17 b-estradiol ; ER-estrogen receptor; S ARM-selective androgen receptor modulator; SRB-sulforhodamine B; mpk-milligram per kilogram body weight. Values are expressed as average ± S.E. from n=3-4/data point.

[00070] Figure 35A-Figure 35D depict that AR agonists inhibited proliferation and growth of wildtype and mutant ER and AR -positive xenografts. Figure 35A depicts that protein from HCI PDX (HCI-7, 9, or 13) tumor fragments was extracted and fractionated on a SDS-PAGE, and Western blotted for the AR. AR was also quantified at mRNA level and expressed as fold change from LNCaP prostate cancer cell AR (numbers provided under the blot). Figures 35B (same as Figure 32) and Figure 35C depict that Formula IX inhibited HCI-7 tumor growth. AR- positive HCI-7 PDX expressing wildtype ER was surgically implanted as 1 mm ³ fragments under the mammary fat pad in NSG mice (n=8- 10/group). Once the tumors reached 100-200 mm ³ , the mice were randomized and treated with vehicle (DMSO:PEG-300 (15%:85%)), Formula IX (10 mpk p.o.), or enzalutamide (30 mpk p.o.). Tumor volume was measured weekly. At sacrifice, tumors were removed, weighed (Figure 35C), and stored for further analysis. Figure 35D depicts that MCF-7 cells (3 million cells/mouse) stably expressing AR (MCF-7-AR) were implanted subcutaneously in ovariectomized mice supplemented with 17b- estradiol (n=8/group). Once the tumors reached 100-200 mm ³ , the mice were randomized and treated with vehicle or Formula IX (10 mpk p.o.). Tumor volume was measured twice weekly. *=p<0.05; HCI-Huntsman Cancer Institute; AR-androgen receptor; ER-estrogen receptor; NSG-NOD SCID Gamma; PDX-patient-derived xenograft; OVX-ovariectomy; PR- progesterone receptor; mpk-milligram per kilogram body weight. [00071] Figure 36A -Figure 36K depict that AR agonists inhibited proliferation and growth of mutant ER and AR-positive xenografts. Figure 36A depicts that the growth of HCI-13 PDX was not dependent on circulating estrogens. HCI-13 PDX tumor fragments were surgically implanted as 1 mm ³ fragments under the mammary fat pad in NSG mice (n=6/group) that were sham operated or ovariectomized. Tumor volume was measured weekly. Figure 36B and Figure 36C depict that AR agonist (Formula IX) inhibited growth of HCI-13 PDX. AR-positive HCI- 13 PDX expressing mutant ER was surgically implanted as 1 mm ³ fragments under the mammary fat pad in NSG mice (n=8-10/group). Once the tumors reached 100-200 mm ³ , the mice were randomized and treated with vehicle (DMSO:PEG-300 (15%:85%)) or Formula IX (10 mpk p.o.). Tumor volume was measured weekly. At sacrifice, tumors were removed, weighed (Figure 36C), and stored for further analysis. Figure 36D-Figure 36G depict that AR agonists, but not AR- or ER- antagonists, inhibited ER-target genes in HCI-13 ex vivo sponge culture. HCI-13 tumors (1 mm ³ ) were cultured on gelatin sponges (n=3/group; each n was obtained by pooling 5 fragments) in growth medium. Tissues were treated with vehicle, 10 nM DHT, 1 mM Formula IX, 1 mM enzalutamide, or 100 nM fulvestrant for three days. RNA was extracted from the tissues and expression of genes was measured by real time PCR and normalized to GAPDH. Figure 36H-Figure 36J depict the effect of Formula IX on ER-positive breast cancer patient specimens. Breast cancer specimens obtained from patients were cultured on gelatin sponges (n=l; each n was obtained from 5 tumor fragments). Tissues were treated with vehicle, 1 pM Formula IX, or 100 nM fulvestrant for three days. RNA was extracted from the tissues and expression of genes was measured by real time PCR and normalized to GAPDH. Table in Figure 36K denotes the fold difference in the expression of AR and ER at the mRNA level compared to HCI-13 tumors. *=p<0.05; HCI-Huntsman Cancer Institute; AR-androgen receptor; ER-estrogen receptor; NSG-NOD SCID Gamma; PDX-patient-derived xenograft; MKI67-mRNA of Ki67 proliferative index protein; OVX-ovariectomy; PR-progesterone receptor; mpk-milligram per kilogram body weight.

[00072] Figure 37A-Figure 37H depict a gene expression study in HCI-13 PDX that indicated the inhibition of the ER pathway by an AR agonist. RNA was isolated from HCI-13 PDX xenografts treated with vehicle or Formula IX (Figure 36B -Figure 36C) and microarray was performed (n=4/group). Genes that were different in Formula IX treated group (q<0.05) are represented in the heatmap (upper 1/5 of the left column (vehicle-treated) of the heatmap is predominantly upregulated (originally red) whereas lowered 4/5 of heatmap is predominantly downregulated (originally green); in contrast, the Formula IX treated column is just the opposite (green at top and red at bottom).) (Figure 37A). Log fold change in expression with top up- and down-regulated genes was expressed in panel Figure 37B. Canonical pathway, upstream regulators, and diseases represented by the enriched genes obtained from Ingenuity Pathway Analysis (IP A) were shown in panel Figure 37C. Representative ER- and AR- target genes and the most up- and down- regulated genes were shown in panel Figure 37D-Figure 37G. Figure 37H depicts that the GSEA KEGG pathway analysis provided ERBB2 (ERBB is abbreviated from erythroblastic oncogene B ; also frequently called HER2 (from human epidermal growth factor receptor 2) or HER2/neu) pathway as one of the highly correlated pathway with Formula IX treatment (bottom four rows in the left column (vehicle treated) are downregulated genes (blue in the original color) whereas most of the rows are upregulated genes (red in the original color); in contrast, Formula IX treated column (right) is just the opposite). * = q<0.05; ER- estrogen receptor; AR-androgen receptor; PDX-patient-derived xenograft; GSEA-gene set enrichment analysis; KEGG- Kyoto encyclopedia of genes and genomes.

[00073] Figure 38A-Figure 38H depict that ChIP-Sequencing showed rearrangement of ER and AR binding to the DNA. Figure 38 A depicts that chromatin immunoprecipitation (ChIP) assay was performed with ER in tumors treated with vehicle (n=4) or 10 mg/kg/day Formula IX (n=3) or AR (n=l) (tumors from animals shown in Figure 36B -Figure 36C). Next-generation sequencing was performed to determine the genome-wide binding of ER and AR to the DNA. Heatmap of significantly different peaks (q<0.05 for ER and corresponding AR peaks) is shown. The top enriched motifs are shown in Figure 38H. Figure 38B shows representative peaks from KLK3 regulatory regions from ER and AR ChIP-Seq. Figure 38C shows Principal Component Analysis (PCA) plot of vehicle- and Formula IX -treated samples that corresponds to ER-ChIP peaks. Figure 38D depicts that ChIP assay was performed with AR or ER antibody in HCI-13 specimens treated with vehicle or Formula DC and real time PCR was performed with the primers and Taqman probe to the specified regions. Figure 38E depicts pie charts showing the distribution of ER enrichment in Formula DC -treated HCI-13 samples. For downregulated sites (left pie), ‘distal regulatory regions’ represent 56%, introns 38%, exons 5%, and promoters 2%. For enriched sites (right pie), ‘distal regulatory proteins’ represent 53%, introns 36%, exons 8%, and promoters 3%. Figure 38F depicts Venn diagrams showing the overlap between depleted FOXA1RE and ERE regions and enriched ARE, GRE, and FOXA1RE. Figure 38G depicts that SRC-1 interacted with both AR and ER in response to Formula IX. Protein extracts from HCI-13 tumor samples treated with vehicle or Formula IX were immunoprecipitated with AR or ER antibodies and Western blot for SRC-1 was performed. AR-androgen receptor; ER- estrogen receptor; ChIP- chromatin immunoprecipitation; ARE-androgen response elements; ERE-estrogen response element; GRE-glucocorticoid response elements; SRC-1- steroid receptor coactivator- 1, FOXAIRE-Forkhead box A1 response element. Figure 38H depicts up- regulated motifs (ER).

[00074] Figure 39 depicts colocalization of AR and ER-oc in luminal B breast cancer specimens.

[00075] Figure 40 depicts representative ChIP Seq peaks in the regulated regions of genes. The peaks are color coded with the top panel being predominantly upregulated (red), whereas the 2 ^nd from top panel is downregulated (blue), 3 ^rd panel from top (CERS3) is downregulated except for the last line (IX (AR)), and bottom panel (miR4471) is also downregulated except for the last line (IX (AR)).

[00076] Figure 41A-Figure 41E depict a phospho-proteome analysis of HCI-13 PDX. Figure 41A-Figure 41C depict that lysates from HCI-13 tumor specimens (n=4) from PDX (as shown in Figure 36B-Figure 36C) were printed onto nitrocellulose coated slides. Arrays were probed with a total of 174 antibodies targeting a wide range of protein kinases and their activation via phosphorylation. Arrays were stained with an anti-rabbit or anti-mouse biotinylated secondary antibody. The signals were amplified and a streptavidin-conjugated IRDye680 were used as secondary signal detection agents. Images were acquired and quantified. Figure 41D-Figure 4 IE depict that activation of PKC overcame inhibition by Formula IX. HCI-13 tissues fragments were cultured on gelatin sponges and were treated with 100 nM phorbol 12-myristate 13-acetate (PMA) or 100 ng/mL EGF 30 minutes before addition of 1 mM Formula IX. EGF was treated twice daily due to its shorter stability. Tissues were harvested after 3 days of treatment, RNA isolated, and expression of various genes was measured by real time PCR. * p<0.05 from vehicle-treated samples; # p<0.05 from Formula IX -treated samples. n=3/group (each sample is obtained from 5 individual fragments. PMA- phorbol 12-myristate 13-acetate; EGF-epidermal growth factor; PDX-patient derived xenografts; HCI- Huntsman Cancer Institute.

[00077] Figure 42 shows a model depicting the regulation of ER function by AR agonist. [00078] Figure 43 depicts a scatterplot of radiographic progression free survival (rPFS) vs. % androgen receptor staining at baseline in the clinical trial of Example 30 for a 9 mg dose group with measurable disease at baseline.

[00079] Figures 44A and 44B present that Formula IX (SARM) re-sensitized human breast cancer models to CDK 4/6 inhibition in models of CDK 4/6 resistance. Figure 44A depicts a growth curve of PDX GAR15-13 treated with vehicle (n=8), Formula IX labeled as SARM (n=8), Palbo (n=7), or combination (Combo) SARM + Palbo (n=ll). Astericks denoted significantly different tumor volumes at ethical end point, as determined by a two-tailed, unpaired Student’s t-test, for Palbo versus Combo (z=3.7246, d.f. =14, P=0.0022) and SARM versus Combo (z=4.094, d.f.=15, P=0.0010). Data were presented as mean values ± s.e.m. Figure 44B depicts proliferation of Palb ^R cells in response to AR agonist (Formula IX 100 nM) and Palb (125 nM), alone or in combination. Data represented the mean ± s.e.m. of four replicate cell culture wells per condition. Data were analyzed using a one-way ANOVA ( F = 79.71, d.f. = 23, P < 0.0001) followed by Tukey’s multiple comparisons test. P values are indicated by gray asterisks, where ****P<0.0001 for all highlighted comparisons.

[00080] Figure 45 depicts radiographic progression free survival Kaplan-Meier curves for 9 mg enobosarm dose: Group 1 (Patients with AR nuclei staining <40%) and Group 2 (Patients with AR nuclei staining >40%), showing that the prescreening of cancer samples in patients for >40% AR nuclei staining before treatment with a SARM for ER+/AR+/HER2- metastatic breast cancer has an effect on overall survival.

DETAILED DESCRIPTION OF THE INVENTION

[00081] In one aspect, this invention relates to methods of prescreening then treatment of breast cancers with selective androgen receptor modulators (SARMs). The invention further provides methods of: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then beating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado- trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating, preventing, suppressing or inhibiting AR-positive triple negative breast cancer; r) prescreening then treating a subject suffering from HER2-positive breast cancer; s) prescreening then treating a subject suffering from ER mutant expressing breast cancer, t) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, by administering to the subject a therapeutically effective amount of a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a male. In one embodiment, the subject is a female.

[00082] In one embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, V- oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00083] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from metastatic breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00084] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from refractory breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat refractory breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00085] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00086] In one embodiment, the AR-positive breast cancer is ER, PR and HER2-positive. In another embodiment, the AR-positive breast cancer is ER, PR and HER2-negative. In one embodiment, the AR-positive breast cancer is ER-positive, and PR and HER2-negative. In another embodiment, the AR-positive breast cancer is ER and PR-positive, and HER2-negative. In yet another embodiment, the AR-positive breast cancer is ER and HER2 -positive, and PR- negative. In still another embodiment, the AR-positive breast cancer is ER-negative, and PR and HER2 -positive. In a further embodiment, the AR-positive breast cancer is ER and PR- negative, and HER2-positive. In still a further embodiment, the AR-positive breast cancer is ER and HER2-negative, and PR-positive. In one embodiment, the AR-positive breast cancer is ER-negative. In another embodiment, the AR-positive breast cancer is ER-positive.

[00087] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive refractory breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive refractory breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00088] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive metastatic breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00089] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00090] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from ER-positive breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat ER-positive breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00091] In one embodiment, the ER-positive breast cancer is AR-positive. In another embodiment, the ER-positive breast cancer is AR-negative. In one embodiment, ER-positive breast cancer is triple positive (ER, PR, HER2) breast cancer. In another embodiment, ER- positive breast cancer is not triple positive breast cancer.

[00092] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from triple negative breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat triple negative breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00093] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive triple negative breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to AR-positive treat triple negative breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00094] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from advanced breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat advanced breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00095] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin- releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado- trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin- releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado- trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00096] In another embodiment this invention provides a method of prescreening then treating a subject suffering from HER2-positive breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N- oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat HER2 -positive breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[00097] In one embodiment, the HER2-positive breast cancer is HER2 -positive refractory breast cancer. In another embodiment, the HER2 -positive breast cancer is HER2 -positive metastatic breast cancer. In one embodiment, the HER2 -positive breast cancer is ER-negative. In another embodiment, the HER2 -positive breast cancer is ER-positive. In one embodiment, the HER2-positive breast cancer is PR-positive. In another embodiment, the HER2-positive breast cancer is PR-negative. In one embodiment, the HER2 -positive breast cancer is AR- positive. In another embodiment, the HER2 -positive breast cancer is AR-negative.

[00098] In certain embodiment, the HER2-positive breast cancer is ER-positive, PR- positive, and AR-positive. In another embodiment, the HER2-positive breast cancer is ER- positive, PR-negative, and AR-positive. In another embodiment, the HER2 -positive breast cancer is ER-positive, PR-negative, and AR-negative. In another embodiment, the HER2- positive breast cancer is ER-positive, PR-positive, and AR-negative. In another embodiment, the HER2-positive breast cancer is ER-negative, PR-negative, and AR-positive. In another embodiment, the HER2 -positive breast cancer is ER-negative, PR-positive, and AR-positive. In another embodiment, the HER2 -positive breast cancer is ER-negative, PR-positive, and AR- negative. In certain embodiment, the HER2-positive breast cancer is ER-negative, PR- negative, and AR-negative. In certain embodiment, the HER2 -positive breast cancer is triple- positive HER2 breast cancer. [00099] In another embodiment this invention provides a method of prescreening then and treating a subject suffering from ER mutant expressing breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat ER mutant expressing breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000100] In a certain embodiment, the ER mutant expressing breast cancer is Y537S mutation expressing breast cancer.

[000101] In a certain embodiment, the ER mutant expressing breast cancer is D351Y mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is E380Q mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is V422del mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is S432L mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is G442A mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is S463P mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L469V mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536R mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536H mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536P mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536Q mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is Y537N mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is Y537C mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is Y537D mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is D538G mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is E542G mutation expressing breast cancer. In one embodiment, ER mutant expressing breast cancer refers to mutants of ER-alpha.

[000102] In a certain embodiment, the ER mutant expressing breast cancer is as described in Cancer Cell 2018, 33, 173-186, or in Nat Rev Cancer 2018, 18(6):377-388, which are incorporated herein by reference. In one embodiment, ER mutant expressing breast cancer refers to mutants of ER-alpha.

[000103] In one aspect, this invention provides a method of prescreening a breast cancer in a subject for whether said breast cancer is susceptible to selective androgen receptor modulator (SARM) treatment, comprising obtaining a biological sample from said subject prior to said SARM treatment and analyzing for whether said sample has an androgen receptor (AR)- positive staining. In some embodiments, the SARM for the treatment is a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate,N-oxide , crystal, polymorph, prodrug or any combination thereof. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 40%, or 50%, or 60%, or 70%, or 80%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 30%. In other embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 55%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 65%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 75%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 80%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 85%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 90%.

[000104] In one aspect, this invention provides a method of prescreening a breast cancer in a subject for whether said breast cancer is susceptible to selective androgen receptor modulator (SARM) treatment, comprising obtaining a biological sample from said subject prior to said SARM treatment and analyzing for whether said sample has a percent androgen receptor (AR)- positive staining above a threshold value. In some embodiments, the SARM for the treatment is a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-ox, i cdreystal, polymorph, prodrug or any combination thereof. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 40%, or 50%, or 60%, or 70%, or 80%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 55%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 65%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 75%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 80%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 85%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 90%.

[000105] In one aspect, the invention provides a method of treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM), comprising analyzing a biological sample obtained from said subject prior to treatment to determine whether said sample has an androgen receptor (AR)-positive staining then administering to said subject a therapeutically effective amount of the selective androgen receptor modulator (SARM). In some embodiments, the biological same is analyzed for whether AR-positive staining is above a threshold level. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 40%, or 50%, or 60%, or 70%, or 80% In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 30%. In other embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 55%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 65%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 75%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 80%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 85%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 90%. In some embodiments, the SARM is a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N- oxide, crystal, polymorph, prodrug or any combination thereof. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000106] In one aspect, this invention provides method of treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM), comprising analyzing a biological sample obtained from said subject prior to treatment to determine whether said sample has a percent androgen receptor (AR)-positive staining above a threshold value then administering to said subject a therapeutically effective amount of the selective androgen receptor modulator (SARM). In some embodiments, the SARM is a compound of Formulae I- XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 40%, or 50%, or 60%, or 70%, or 80%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 55%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 65%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 70%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 75%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 80%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 85%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 90%.

[000107] In some embodiments of the method of the invention, e.g., the method of prescreening a breast cancer of the invention then treating said breast cancer of the invention, the SARM compound is represented by a structure of formula I:

I wherein X is a bond, O, CH ₂ , NH, S, Se, PR, NO, or NR;

G is O or S;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl, or OH; Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ;

R ₂ is H, F, Cl, Br, I, CH ₃ , CF ₃ , OH, CN, N0 ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, alkyl, arylalkyl, OR, NH ₂ , NHR, N(R) ₂ , or SR;

R ₃ is H, F, Cl, Br, I, CN, N0 ₂ , COR, COOH, CONHR, CF ₃ , Sn(R) ₃ , or R ₃ together with the benzene ring to which it is attached forms a fused ring system represented by the structure:

Z is N0 ₂ , CN, COR, COOH, or CONHR;

Y is CF ₃ , F, Br, Cl, I, CN, or Sn(R) ₃ ; Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH3, NHCSCF3, NHCSR, NHSO2CH3, NHSO2R, OR, COR, OCOR, OSO2R, SO2R, or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C: n is an integer of 1-4; and m is an integer of 1-3, or an optical isomer, a racemic mixture, a pharmaceutically acceptable salt, a pharmaceutical product, a hydrate, an N-oxide, or a crystal thereof.

[000108] In some embodiments, the SARM compound is represented by a structure of formula II: wherein

X is a bond, O, CH ₂ , NH, Se, PR, or NR;

G is O or S;

T is OH, OR, -NHCOCH3, or NHCOR; Z is NO2, CN, COR, COOH, or CONHR;

Y is I, CF ₃ , Br, Cl, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHSO ₂ CH ₃ , NHSO ₂ R,

OR, COR, OCOR, OSO2R, SO2R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C;

R is a C1-C4 alkyl, aryl, phenyl, alkenyl, hydroxyl, a C1-C4 haloalkyl, halogen, or haloalkenyl; and Ri is CH ₃ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ .

[000109] In some embodiments, the SARM compound is represented by a structure of formula VIII, IX, X, XI, XII, XIII, or XIV:

XI,

XIV.

[000110] In some embodiments, the SARM compound is represented by a structure of formula IX:

IX.

[000111] In some embodiments of the method of prescreening then treatment of a breast cancer of the invention, the breast cancer is an AR-positive breast cancer, ER-positive breast cancer, triple negative breast cancer, HER2-positive breast cancer, advanced breast cancer, refractory breast cancer, metastatic breast cancer, or breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof

[000112] In some embodiments, the breast cancer is AR-positive metastatic breast cancer. In other embodiments, the breast cancer is AR-positive refractory breast cancer. In some embodiments, the breast cancer is AR-positive and ER-positive breast cancer. In other embodiments, the breast cancer is AR-negative and ER-positive breast cancer.

[000113] In some embodiments, the ER-positive breast cancer is AR-positive and ER-positive breast cancer. In other embodiments, the ER-positive breast cancer is AR-negative and ER- positive breast cancer. [000114] In some embodiments, the AR-positive breast cancer is ER-negative; ER-negative,

PR-negative, and HER2-negative; ER-negative, PR-negative, and HER2-positive; ER- negative, PR-positive, and HER2-negative; ER-negative, PR-positive, and HER2 -positive; ER- positive, PR-negative, and HER2-negative; ER-positive, PR-positive, and HER2-negative; ER- positive, PR-negative, and HER2-positive; or ER-positive, PR-positive, and HER2 -positive. [000115] In some embodiments, the method of the invention further prolongs the survival of the subject suffering from breast cancer or prolongs the progression-free survival of the subject suffering from breast cancer.

[000116] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 2% to 100%, or from 5% to 100%, or from 10% to 100%, or from 15% to about 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100% or from 55% to 100%, or from 60% to 100%, or from 65% to 100%, or from 70% to 100%. In other embodiments, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 10% to 100%, or from 15% to 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to

100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to

100%, or from 55% to 100%, or from 60% to 100%, or from 65% to 100%, or from 70% to

100%. In other embodiments, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 10% to 100%, or from 15% to 100%, or from 20% to

100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to

100%, or from 45% to 100%, or from 50% to 100%, or from 55% to 100%, or from 60% to

100%, or from 65% to 100%, or from 70% to 100%, or from 75% to 100%, or from 80% to

100%, or from 85% to 100%, or from 90% to 100%. In other embodiments, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 10% to 100%, or from 15% to 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 60% to 100%, or from 70% to 100%.

[000117] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of greater than or equal to 2%, or greater than or equal to 5%, or greater than or equal to 7%, or greater than or equal to 10%, or greater than or equal to 15%, or greater than or equal to 20%, or greater than or equal to 25%, or greater than or equal to 30%, or greater than or equal to 35%, or greater than or equal to 40%, or greater than or equal to 45%, or greater than or equal to 50%, or greater than or equal to 55%, or greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%.

[000118] In other embodiments, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of greater than or equal to 10%, greater than or equal to 15%, greater than or equal to 20%, greater than or equal to 25%, greater than or equal to 30%, greater than or equal to 35%, greater than or equal to 40%, or greater than or equal to 45%, or greater than or equal to 50%, or greater than or equal to 55%, or greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%. In other embodiments, the biological sample obtained from the subject said sample has an androgen receptor (AR)-positive staining of greater than or equal to 10%, greater than or equal to 15%, greater than or equal to 20%, greater than or equal to 25%, greater than or equal to 30%, greater than or equal to 35%, greater than or equal to 40%, or greater than or equal to 45%, or greater than or equal to 50%, greater than or equal to 60%, or greater than or equal to 70%.

[000119] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of greater than or equal to 35%, or greater than or equal to 45%, or greater than or equal to 50%, or greater than or equal to 60%, or greater than or equal to 70%.

[000120] In some embodiments, the average radiographic progression free survival after said treatment is for greater than or equal to 3 months, or for greater than or equal to 4 months, or for greater than or equal to 5.0 months, or for greater than or equal to 6.0 months, or for greater than or equal to 8.0 months, or for greater than or equal to 9.0 months, or for greater than or equal to 10 months, or for greater than or equal to 12 months, or for greater than or equal to 1.5 years, or for greater than or equal to 2.0 years, or for greater than or equal to 2.5 years, or for greater than or equal to 3.0 years, or for greater than or equal to 5.0 years, or for greater than or equal to 10 years.

[000121] In some embodiments, the average radiographic progression free survival after said treatment is for greater than or equal to 3 months, or for greater than or equal to 4 months, or for greater than or equal to 6.0 months, or for greater than or equal to 12 months, or for greater than or equal to 1.5 years, or for greater than or equal to 2.0 years, or for greater than or equal to 2.5 years, or for greater than or equal to 3.0 years, or for greater than or equal to 5.0 years, or for greater than or equal to 10 years. In other embodiments, the average radiographic progression free survival after said treatment is for greater than or equal to 3 months, or for greater than or equal to 4 months, or for greater than or equal to 6.0 months, or for greater than or equal to 12 months, or for greater than or equal to 1.5 years, or for greater than or equal to 2.0 years, or for greater than or equal to 2.5 years, or for greater than or equal to 3.0 years. [000122] As used herein, in some embodiments, the term “average radiographic progression free survival” refers to the average/mean time period that elapses on study while a patient does not have a progression in their disease. The progression in this case is detected radiographically using scans such as a CT scan, MRI or bone scan. [000123] In some embodiments, the clinical benefit response rate of said treatment is at least

20%, is at least 30%, is at least 40%, or is at least 60%, or at least 70%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or about 100%. In other embodiments, the clinical benefit response rate of said treatment is at least 20%, or is at least 30%, at least 40%, or is at least 60%, or at least 70%, or at least 80%, or at least 85%, or at least 90%. [000124] As used herein, in some embodiments, the term “clinical benefit response rate” refers to the percentage of patients that have an objective response (partial responses (PR) or complete responses (CR) per RECIST criteria) or stable disease (SD) while on study. Therefore, it is the people that have not progressed.

[000125] In some embodiments of the method of the invention, the subject has previously received a chemotherapy. In some embodiments, the subject has previously received a non- endocrine based chemotherapy.

[000126] In some embodiments of the method of the invention, the subject has failed a prior treatment. In other embodiments, the subject has failed two prior treatments. In other embodiments, the subject has failed three to five prior treatments. In other embodiments, the subject has failed more than five prior treatments.

[000127] In some embodiments of the method of the invention, the subject has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof.

[000128] In some embodiments, the subject has failed treatment with a selective estrogen receptor modulator (SERM). In some embodiments, the SERM is tamoxifen, toremifene, or raloxifene.

[000129] In some embodiments, the subject has failed treatment with a cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor. In other embodiments, the subject is resistant or non-responsive to the CDK 4/6 inhibitor. In some embodiments, the CDK 4/6 inhibitor is palbociclib (Ibrance), ribociclib (Kisqali), trilaciclib, lerociclib, or abemaciclib (Vorzenio). In some embodiments, the CDK 4/6 inhibitor is palbociclib (Ibrance). In some embodiments, the CDK 4/6 inhibitor is abemaciclib (Vorzenio).

[000130] In some embodiments of the method of the invention, the SARM compound, or an optical isomer, a racemic mixture, a pharmaceutically acceptable salt, a pharmaceutical product, a hydrate, an N-oxide, or a crystal thereof, is in the form of a pellet, a tablet, a capsule, a solution, a suspension, an emulsion, an elixir, a gel, a cream, a suppository or a parenteral formulation.

[000131] In some embodiments of the method of the invention, the SARM compound of Formulae I-XIV as described herein, or an optical isomer, a racemic mixture, a pharmaceutically acceptable salt, a pharmaceutical product, a hydrate, an N-oxide, or a crystal thereof, is administered intravenously, intraarterially, intramuscularly, subcutaneously, orally, or topically. In some embodiments, the composition of the invention is administered orally.

[000132] In some embodiments of the method of the invention, the selective androgen receptor modulator is dosed from 1 mg to 50 mg per day, or from 1 mg to 40 mg per day, or from 1 mg to 30 mg per day, or from 1 mg to 25 mg per day, or from 1 mg to 20 mg per day. In some embodiments, the selective androgen receptor modulator is dosed at 9 mg per day. In other embodiments, the selective androgen receptor modulator is dosed at 18 mg per day.

[000133] In some embodiments, the selective androgen receptor modulator is dosed from 1 mg to 50 mg per day. In some embodiments, the selective androgen receptor modulator is dosed per day from about 1 mg to about 5 mg, or from about 5 mg to about 50 mg, or from about 5 mg to about 10 mg, or from about 5 mg to about 15 mg, or from about 5 mg to about 20 mg, or from about 5 mg to about 30 mg, or from about 10 mg to about 50 mg, or from about 10 mg to about 40 mg, or from about 10 mg to about 30 mg, or from about 10 mg to about 20 mg, or from about 15 mg to about 50 mg, or from about 20 mg to about 50 mg, or from about 25 mg to about 50 mg, or from about 30 mg to about 50 mg, or from about 30 mg to about 40 mg. In some embodiments, the selective androgen receptor modulator is dosed about 9 mg per day or about 18 mg per day.

[000134] As used herein, in one embodiment the term "treating" may refer to treating, delaying the progression, preventing the recurrence or treating the recurrence. In one embodiment, the term "treating" refers to a reduction in morbidity, mortality, or a combination thereof, in association with breast cancer.

[000135] The term “preventing” may refer to preventing the initial occurrence of a disorder, reducing risk factors, minimize the disability or potential health threat of a disorder.

[000136] As used herein, the term "breast cancer" may refer to breast cancer; advanced breast cancer; metastatic breast cancer; AR-positive breast cancer; ER-positive breast cancer; AR- positive breast cancer with or without expression of ER, PR and/or HER2; triple-positive breast cancer (ER, PR and HER2-positive), AR-positive breast cancer with or without expression of ER; ER-positive breast cancer with or without expression of AR; AR-positive and ER-positive breast cancer; refractory breast cancer; AR-positive refractory breast cancer; ER-positive refractory breast cancer; AR-positive metastatic breast cancer; ER-positive metastatic breast cancer; breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; or triple negative breast cancer; or any combination thereof.

[000137] In one embodiment, the term "breast cancer" refers to a condition characterized by anomalous rapid proliferation of abnormal cells in one or both breasts of a subject. The abnormal cells often are referred to as “neoplastic cells,” which refers to, in some embodiments, transformed cells that can form a solid tumor. The term “tumor”, in some embodiments, refers to an abnormal mass or population of cells (i.e., two or more cells) that result from excessive or abnormal cell division, whether malignant or benign, and pre-cancerous and cancerous cells. Malignant tumors are distinguished from benign growths or tumors in that, in addition to uncontrolled cellular proliferation, they can invade surrounding tissues and can metastasize.

[000138] In breast cancer, neoplastic cells may be identified in one or both breasts only and not in another tissue or organ, in one or both breasts and one or more adjacent tissues or organs (e.g., lymph node), or in a breast and one or more non-adjacent tissues or organs to which the breast cancer cells have metastasized.

[000139] The term “metastasis”, in some embodiments, refers to a process in which cancer cells travel from one organ or tissue to another non-adjacent organ or tissue. Cancer cells in the breast(s) can spread to tissues and organs of a subject, and conversely, cancer cells from other organs or tissue can invade or metastasize to a breast. Cancerous cells from the breast(s) may invade or metastasize to any other organ or tissue of the body. Breast cancer cells often invade lymph node cells and/or metastasize to the liver, brain and/or bone and spread cancer in these tissues and organs. The term “invasion”, in some embodiments, refers to the spread of cancerous cells to adjacent surrounding tissues. [000140] As used herein, the term "advanced breast cancer" refers to cancer that has spread to other places in the body and usually cannot be cured or controlled with current treatment.

[000141] As used herein, the term "AR-positive breast cancer" may refer to breast cancer wherein at least a portion of the cancer cells express at least the androgen receptor (AR). [000142] As used herein, the term "ER-positive breast cancer" may refer to breast cancer wherein at least a portion of the cancer cells express at least the estrogen receptor (ER).

[000143] As used herein, the term "triple negative breast cancer" may refer to breast cancer cells that do not have estrogen receptors (ER), progesterone receptors (PR), or large amounts of HER2/neu protein. "Triple negative breast cancer" may also be referred to herein as "ER- negative PR-negative HER2/neu-negative breast cancer".

[000144] As used herein, the term "triple positive breast cancer" may refer to breast cancer cells that express estrogen receptors (ER), progesterone receptors (PR), and large amounts of HER2/neu (HER2) protein. "Triple positive breast cancer" may also be referred to herein as "ER-positive PR-positive HER2/neu-positive breast cancer" or “ER, PR, and HER2 breast cancer”.

[000145] As used herein, the term "refractory" may refer to breast cancer that does not respond to treatment. The breast cancer may be resistant at the beginning of treatment or it may become resistant during treatment. "Refractory breast cancer" may also be referred to herein as "resistant cancer". [000146] As used herein, the term “HER2 -positive breast cancer” may refer to breast cancers wherein at least a portion of the cancer cells express elevated levels of HER2 protein (HER 2 (from human epidermal growth factor receptor 2) or HER2/neu) which promotes rapid growth of cells.

[000147] As used herein, the term “ER mutant expressing breast cancer” may refer to breast cancers that express estrogen receptor alpha (ER-oc) with therapy resistance conferring mutations. Often these mutations are located within the ligand binding domain of ER-oc, are treatment emergent, and/or confer resistance to certain or all endocrine therapies such as SERMs, AIs, SERDs, and/or GnRH agonists. As used herein, the term “Y537S ER mutant expressing breast cancer” may refer to breast cancers that express estrogen receptor alpha (ER-α ) with the point mutation Y537S.

[000148] In another embodiment of the present invention, a method is provided for prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat, prevent, suppress or inhibit metastasis in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000149] In another embodiment of the present invention, a method is provided for prescreening then prolonging the survival of a subject with breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to prolong the survival of a subject with breast cancer. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000150] In another embodiment of the present invention, a method is provided for prescreening then slowing the progression of breast cancer in a subject, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to slow the progression of breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000151 ] In another embodiment of the present invention, a method is provided for prescreening then prolonging progression-free survival of a subject with breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to prolong progression-free survival of a subject with breast cancer. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000152] In one embodiment, breast cancer of this invention refers to in one embodiment to ER-positive metastatic breast cancer. In another embodiment to ER-positive refractory breast cancer. In another embodiment to ER-positive PR-positive HER2-negative breast cancer. In another embodiment to AR-positive ER-positive breast cancer. In another embodiment to AR- positive ER-positive refractory breast cancer. In another embodiment to AR-positive ER- positive metastatic breast cancer. In another embodiment to triple positive breast cancer. In another embodiment to advanced ER-positive breast cancer; In another embodiment to AR- positive. In another embodiment to ER-positive breast cancer. In another embodiment to breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof.

[000153] In another embodiment of the present invention, a method is provided for lowering biomarker levels in a subject with breast cancer comprising the step of administering to the subject a compound of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N- oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to lower the biomarker level in said subject. In another embodiment, the method comprises administering a compound of Formulae I-XIV of this invention. As used herein, the term “biomarker” may refer to a substance used as an indicator of a process, event, or condition. A biomarker can be a biomolecule such as a nucleic acid molecule (e.g., microRNA, genomic DNA, etc.), a protein, a polysaccharide, and the like. Biomarkers include tumor antigens and tumor markers. In one embodiment, a biomarker indicates the presence of cancer, e.g., breast cancer. In one embodiment, a biomarker may be used to determine the efficacy of treatment. In one embodiment, a biomarker may be used to determine the progression of a condition, e.g., breast cancer.

[000154] The MUC-1 associated antigen, or CA 27.29, is a cancer antigen highly associated with breast cancer. As used herein, the term “CA27.29 biomarker” refers to a biomarker for breast cancer. In one embodiment, CA27.29 is a biomarker for advanced breast cancer.

[000155] “PSA (prostate- specific antigen) biomarker” is used as a biomarker for prostate cancer, however PSA was also found in the blood of women with breast cancer at higher levels compared to women without breast cancer. PSA is useful also as a biomarker for breast cancer.

[000156] “CTX biomarker” and “NTX biomarker” are the C-telopeptide and N-telopeptide of collagen type I, respectively, which are used as biomarkers of bone turnover. NTX and CTX biomarkers may be sensitive indicators of the presence of bone metastases in breast cancer patients.

[000157] In one embodiment, a method of this invention lowers CA27.29 biomarker in a subject. In one embodiment, a method of this invention lowers PSA in a subject. In one embodiment, a method of this invention lowers CTX biomarker in a subject. In one embodiment of this invention, a method of this invention lowers NTX biomarker in a subject. In another embodiment, a method of this invention maintains the level of CA27.29 in a subject. In another embodiment, a method of this invention maintains the level of PSA in a subject. In another embodiment, a method of this invention maintains the level of CTX biomarker in a subject. In another embodiment, a method of this invention maintains the level of NTX biomarker. In one embodiment, the subject has breast cancer. In one embodiment, the subject has advanced breast cancer. In another embodiment, the subject has refractory breast cancer. In yet another embodiment, the subject has AR-positive breast cancer. In still another embodiment, the subject has ER-positive breast cancer. [000158] In one embodiment, the SARM compound of Formulae I-XIV as described herein is an antagonist. In another embodiment, the SARM compound of Formulae I-XIV as described herein is an agonist. In yet another embodiment, the SARM compound of Formulae I-XIV as described herein is a partial agonist/partial antagonist. In one embodiment, a SARM compound of Formulae I-XIV as described herein is an AR agonist. In another embodiment, a compound is an AR antagonist. In yet another embodiment, a compound is a partial AR agonist and AR antagonist. In one embodiment, a SARM compound of Formulae I-XIV as described herein is a PR agonist. In another embodiment, a SARM compound of Formulae I-XIV as described herein is a PR antagonist. In yet another embodiment, a SARM compound of Formulae I-XIV as described herein is a partial PR agonist and PR antagonist.

[000159] In one embodiment, a SARM compound of Formulae I-XIV as described herein is an AR agonist and a PR antagonist.

[000160] As used herein, “estrogen-deprivation therapy” may refer to therapy which is given in response to breast cancer in a subject. Known treatments include treatment with GnRH agonists, SERMs, SERDs, or aromatase inhibitors (AI). For example, and in one embodiment, the compounds as herein described are useful in treating a bone-related disorder that arises as a result of cancer metastasis to bone, or in another embodiment, as a result of estrogen- deprivation therapy, for example, given in response to breast cancer in the subject. Menopause can also be induced using GnRH agonists such as gosarelin (Zoladex) which maintains endogeneous estrogens at low levels via inhibition of the hypothalamus-pituitary-gonadal axis.

[000161] In one embodiment, this invention provides for the treatment, prevention, suppression or inhibition of, or the reduction of the risk of developing a skeletal-related event (SRE), such as bone fractures, surgery of the bone, radiation of the bone, spinal cord compression, new bone metastasis, bone loss, or a combination thereof in a subject with cancer, comprising administering a compound as herein described and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, or any combination thereof. The invention relates, inter alia, to treatment of an SRE with the compound of Formulae I-XIV as described herein: (a) in a subject with prostate cancer undergoing or having undergone androgen deprivation therapy (ADT); or (b) in a subject with breast cancer undergoing or having undergone estrogen-deprivation therapy. [000162] In one embodiment, the skeletal-related events treated using the methods provided herein and/or utilizing the compositions provided herein, are fractures, which in one embodiment, are pathological fractures, non-traumatic fractures, vertebral fracture, non- vertebral fractures, morphometric fractures, or a combination thereof. In some embodiments, fractures may be simple, compound, transverse, greenstick, or comminuted fractures. In one embodiment, fractures may be to any bone in the body, which in one embodiment, is a fracture in any one or more bones of the arm, wrist, hand, finger, leg, ankle, foot, toe, hip, collar bone, or a combination thereof. In breast cancer, metastasis occurs most often to the hip and vertebrae. In one embodiment, the skeletal-related is fractures to the hip and/or vertebrae.

[000163] In another embodiment, the methods and/or compositions provided herein, are effective in treatment, prevention, suppression, inhibition or reduction of the risk of skeletal- related events such as pathologic fractures, spinal cord compression, hypercalcemia, bone- related pain, or their combination.

[000164] In another embodiment, the skeletal-related events sought to be treated using the methods provided herein and/or utilizing the compositions provided herein, comprise the necessity for bone surgery and/or bone radiation, which in some embodiments, is for the treatment of pain resulting in one embodiment from bone damage, or nerve compression. In another embodiment, the skeletal-related events sought to be treated using the methods provided herein and/or utilizing the compositions provided herein, comprise spinal cord compression, or the necessity for changes in antineoplastic therapy, including changes in hormonal therapy, in a subject. In some embodiments, skeletal-related events sought to be treated using the methods provided herein and/or utilizing the compositions provided herein, comprise treating, suppressing, preventing, reducing the incidence of, or delaying progression or severity of bone metastases, or bone loss. In one embodiment, bone loss may comprise osteoporosis, osteopenia, or a combination thereof. In one embodiment, skeletal-related events may comprise any combination of the embodiments listed herein.

[000165] In one embodiment, the methods provided herein and/or utilizing the compositions provided herein, are effective in reducing metastases to the bone, such as in terms of number of foci, the size of foci, or a combination thereof. According to this aspect of the invention and in one embodiment, provided herein is a method of preventing or inhibiting cancer metastasis to bone in a subject, comprising the step of administering to the subject a composition comprising toremifene, raloxifene, tamoxifen or an analogue, functional derivative, metabolite or a combination thereof, or a pharmaceutically acceptable salt thereof. In one embodiment, such metabolites may comprise ospemifene, fispemifene or their combination. In one embodiment, the cancer is prostate cancer. In one embodiment, the cancer is breast cancer.

[000166] In one embodiment, the skeletal-related events are a result of cancer therapy. In one embodiment, the skeletal-related events are a result of hormone deprivation therapy, while in another embodiment, they are a product of androgen deprivation therapy (ADT), and in another embodiment they are a product of estrogen-deprivation therapy

[000167] As used herein, the term “libido”, may refer to sexual desire, or as defined in Example 9.

[000168] As used herein, the term "quality of life" may refer to the focuses on the health and life of a subject suffering from a condition or disease, for example suffering from breast cancer, post treatment until the end of life. It covers the physical, psychosocial, and economic issues faced by the subject, beyond the diagnosis and treatment phases. The term "quality of life" may also be referred to herein as "survivorship". In one embodiment, survivorship includes issues related to the ability to get health care and follow-up treatment, late effects of treatment, second cancers, and quality of life. Family members, friends, and caregivers are also considered part of the survivorship experience.

[000169] In one embodiment, the methods of this invention are useful to a subject, which is a human. In one embodiment, the subject is male. In another embodiment, the subject is female. In some embodiments, while the methods as described herein may be useful for treating either males or females, females may respond more advantageously to administration of certain compounds, for certain methods. In other embodiments, while the methods as described herein may be useful for treating either males or females, males may respond more advantageously to administration of certain compounds, for certain methods.

Selective Androgen Receptor Modulator (SARM) Compounds and Uses Thereof

[000170] In one aspect, this invention provides a method of prescreening a breast cancer in a subject for whether said breast cancer is susceptible to selective androgen receptor modulator (SARM) treatment, comprising obtaining a biological sample from the subject prior to the SARM treatment and analyzing for whether said sample has an androgen receptor (AR)- positive staining.

[000171] In one aspect, this invention provides a method of prescreening a breast cancer in a subject for whether said breast cancer is susceptible to selective androgen receptor modulator (SARM) treatment, comprising obtaining a biological sample from said subject prior to said SARM treatment and analyzing for whether said sample has a percent androgen receptor (AR)- positive staining above a threshold value. In some embodiments, the threshold value refers to when the treatment occurs the percent AR-positive staining, e.g., greater than or equal to 5%, or 10%, or 15%, or 20%, or 25%, or 30%, 35%, or 40%, or 45%, or 50%, or 55%, or 60%, or 65%, or 70%, or 75%, or 80%.

[000172] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 2% to 100%, or from 5% to 100%, or from 10% to 100%, or from 15% to 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 55% to 100%, or from 60% to 100%, or from 65% to 100%, or from 70% to 100%. In other embodiments, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 10% to 100%, or from 15% to

100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to

100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 55% to

100%, or from 60% to 100%, or from 65% to 100%, or from 70% to 100%, or from 75% to

100%, or from 80% to 100%, or from 85% to 100%, or from 90% to 100%.

[000173] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of greater than or equal to 2%, or greater than or equal to 5%, or greater than or equal to 7%, or greater than or equal to 10%, or greater than or equal to 15%, or greater than or equal to 20%, or greater than or equal to 25%, or greater than or equal to 30%, or greater than or equal to 35%, or greater than or equal to 40%, or greater than or equal to 45%, or greater than or equal to 50%, or greater than or equal to 55%, or greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%. [000174] In some embodiments, patients with a high percentage of AR staining, e.g., greater than or equal to 5%, or 10%, or 15%, or 20%, or 25%, or 30%, or 35%, or greater than or equal to 40%, or greater than or equal to 50%, or greater than or equal to 60%, or greater than or equal to 70%, have longer responses to the treatments with a SARM compound as well as a pharmaceutical composition comprising a SARM compound and an additional therapeutic agent as described herein. For example, such patients have a doubled median radiographic PFS (radiographic progression free survival), e.g., about 8-9 months, whereas patients with a lower AR staining, e.g., less than 40%, progress in 3 months or less.

[000175] In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 35%, or 40%, or 50%, or 60%, or 70%, or 80% In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR- positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 35%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 55%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 65%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 70%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 75%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 80%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 85%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 90%. [000176] In another aspect, the invention provides a method of treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM) compound, comprising analyzing a biological sample obtained from the subject prior to treatment to determine whether said sample has an androgen receptor (AR)-positive staining and then administering to the subject the selective androgen receptor modulator (SARM) compound if the percent AR-positive staining is above a threshold value.

[000177] In one aspect, this invention provides a method of treating a breast cancer in a subject in need thereof with a selective androgen receptor modulator (SARM), comprising analyzing a biological sample obtained from said subject prior to treatment to determine whether said sample has a percent androgen receptor (AR)-positive staining above a threshold value then administering to said subject a therapeutically effective amount of the selective androgen receptor modulator (SARM). In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 10%, or 15%, or 20%, or 25%, or 30%, or 35%, or 40%, or 50%, or 60%, or 70%, or 80%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 5%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 10%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 15%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 20%. In some embodiments, the treatment occurs if the AR-positive staining is greater than or equal to 25%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 30%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 35%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 40%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 45%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 50%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 55%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 60%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 65%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 70%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 75%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 80%. In some embodiments, the treatment occurs if the percent AR- positive staining is greater than or equal to 85%. In some embodiments, the treatment occurs if the percent AR-positive staining is greater than or equal to 90%.

[000178] As used herein, in some embodiments, the term “androgen receptor positive staining” refers to the positive signal that is observed using immunohistochemicai analysis with a monoclonal antibody that recognizes the N-terminal portion of the androgen receptor (AR). The number of positive nuclei is counted and that is divided by the total number of nuclei/cells in the area being analyzed.

[000179] Methods for analyzing a biological sample to measure the percentage and intensity of AR-positive staining are well known in the art (e.g., Rangel et al. Cells, 2020, 9, 1064). Staining of AR is generally considered positive when >1% of tumor cell nuclei are stained. Such values are prognostic and not used as a prescreen to determine whether a patient is to receive a therapy in the art. Currently there are no selective androgen receptor modulators (SARMs) approved for any use, much less for use in any type of breast cancer. Further, this invention demonstrated that treatment of breast cancers with % AR-positive staining <40% are not correlated with a substantial clinical benefit response ratio (CBRR) nor substantial delayed radiographic progression free survival (rPFS). The methods of the invention allow the skilled in the art to apply a clinical threshold value of % AR staining to patients to enrich the CBRR and rPFS associated with SARM treatment. Patients with % AR staining below the threshold may be better served with by a therapy other than SARM treatment.

[000180] It is one aspect of the present invention that androgen receptor is used as a target for prescreening then treatment of breast cancers in a subject prior to treatments with a selective androgen receptor modulator (SARM) compound of Formulae I-XIV as described herein. Surprisingly, it is discovered that there is correlation between the percentage of AR staining in a biological sample obtained from a patient in need of treatment and the efficacy of the SARM compounds as described herein in the treatment. In some embodiments, patients with a high percentage of AR staining, e.g., greater than or equal to 40%, have longer responses to the treatments with a SARM compound as described herein. For example, such patients have a doubled median radiographic PFS (radiographic progression free survival), e.g., about 8-9 months, whereas patients with a lower AR staining, e.g., less than 40%, progress in 3 months or less. [000181] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 2% to 100%, or from 5% to 100%, or from 10% to 100%, or from 15% to 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%.

[000182] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 2% to 100%, or from 5% to 100%, or from 10% to 100%, or from 15% to 100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to 100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 55% to 100%, or from 60% to 100%, or from 65% to 100%, or from 70% to 100%. In other embodiments, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of from 10% to 100%, or from 15% to

100%, or from 20% to 100%, or from 25% to 100%, or from 30% to 100%, or from 35% to

100%, or from 40% to 100%, or from 45% to 100%, or from 50% to 100%, or from 55% to

100%, or from 60% to 100%, or from 65% to 100%, or from 70% to 100%, or from 75% to

100%, or from 80% to 100%, or from 85% to 100%, or from 90% to 100%.

[000183] In some embodiments of the method of the invention, the biological sample obtained from the subject has an androgen receptor (AR)-positive staining of greater than or equal to 2%, or greater than or equal to 5%, or greater than or equal to 7%, or greater than or equal to 10%, or greater than or equal to 15%, or greater than or equal to 20%, or greater than or equal to 25%, or greater than or equal to 30%, or greater than or equal to 35%, or greater than or equal to 40%, or greater than or equal to 45%, or greater than or equal to 50%, or greater than or equal to 55%, or greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%.

[000184] In one embodiment, the SARM compound as described herein which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; and/or p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2-positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula I, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxid,e crystal, polymorph, prodrug or any combination thereof:

I

X is a bond, O, CH ₂ , NH, S, Se, PR, NO, or NR;

G is O or S; T is OH, OR, -NHCOCH3, or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF3, CF ₂ CF3, aryl, phenyl, halogen, alkenyl, or OH;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ;

R ₂ is H, F, Cl, Br, I, CH ₃ , CF ₃ , OH, CN, N0 ₂ , NHCOCH3, NHCOCF3, NHCOR, alkyl, arylalkyl, OR, NH ₂ , NHR, N(R) ₂ , or SR;

R ₃ is H, F, Cl, Br, I, CN, N0 ₂ , COR, COOH, CONHR, CF ₃ , Sn(R) ₃ , or R ₃ together with the benzene ring to which it is attached forms a fused ring system represented by the structure:

Z is N0 ₂ , CN, COR, COOH, or CONHR; Y is CF ₃ , F, Br, Cl, I, CN, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH3, NHCOCF3, NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH3, NHCSCF3, NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R, or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C; n is an integer of 1-4; and m is an integer of 1-3. [000185] In one embodiment, this invention relates to prescreening then treating of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR- positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prescreening then prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER- positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER- positive breast cancer; h) prescreening then treating a subject suffering from refractory ER- positive breast cancer; i) prescreening then treating a subject suffering from AR-positive ER- positive breast cancer; j) prescreening then treating a subject suffering from AR-positive ER- positive refractory breast cancer; k) prescreening then treating a subject suffering from AR- positive ER-positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2-positive breast cancer; u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula I:

I

X is a bond, O, CH ₂ , NH, S, Se, PR, NO, or NR; G is O or S;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl, or OH;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ; R ₂ is H, F, Cl, Br, I, CH ₃ , CF ₃ , OH, CN, N0 ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, alkyl, arylalkyl, OR, NH ₂ , NHR, N(R) ₂ , or SR;

R is H, F, Cl, Br, I, CN, N0 ₂ , COR, COOH, CONHR, CF ₃ , Sn(R) ₃ , or R ₃ together with the benzene ring to which it is attached forms a fused ring system represented by the structure:

Z is N0 ₂ , CN, COR, COOH, or CONHR;

Y is CF ₃ , F, Br, Cl, I, CN, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R, or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C; n is an integer of 1-4; and m is an integer of 1-3; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide , crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000186] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then treating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula I: wherein

X is a bond, O, CH ₂ , NH, S, Se, PR, NO or NR;

G is O or S;

T is OH, OR, -NHCOCH ₃ , or NHCOR; R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ;

R ₂ is H, F, Cl, Br, I, CH ₃ , CF ₃ , OH, CN, N0 ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, alkyl, arylalkyl, OR, NH ₂ , NHR, N(R) ₂ , or SR; R is H, F, Cl, Br, I, CN, N0 ₂ , COR, COOH, CONHR, CF ₃ , Sn(R) ₃ , or R ₃ together with the benzene ring to which it is attached forms a fused ring system represented by the structure:

Z is NO2, CN, COR, COOH, or CONHR;

Y is CF ₃ , F, Br, Cl, I, CN, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R,

OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C; n is an integer of 1-4; and m is an integer of 1-3; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000187] In one embodiment, G in Formula I is O. In another embodiment, X in Formula I is O. In another embodiment, T in Formula I is OH. In another embodiment, Ri in Formula I is CH ₃ . In another embodiment, Z in Formula I is N0 ₂ . In another embodiment, Z in Formula I is CN. In another embodiment, Y in Formula I is CF ₃ . In another embodiment, Y in Formula I is Cl. In another embodiment, Q in Formula I is CN. In another embodiment, Q in Formula I is halogen. In another embodiment, Q in Formula I is F. In another embodiment, Q in Formula I is Cl. In another embodiment, Q in Formula I is NHCOCH ₃ . In another embodiment, Q in Formula I is CN and R ₂ is F. In another embodiment, Q in Formula I is Cl and R ₂ is F. In another embodiment, Q in Formula I is in the para position. In another embodiment, Z in Formula I is in the para position. In another embodiment, Y in Formula I is in the meta position.

[000188] The substituents Z, Y and R ₃ can be in any position of the ring carrying these substituents (hereinafter “A ring”). In one embodiment, the substituent Z is in the para position of the A ring. In another embodiment, the substituent Y is in the meta position of the A ring. In another embodiment, the substituent Z is in the para position of the A ring and substituent Y is in the meta position of the A ring.

[000189] The substituents Q and R2 can be in any position of the ring carrying these substituents (hereinafter “B ring”). In one embodiment, the substituent Q is in the para position of the B ring. In another embodiment, the substituent R2 is in the meta position of the B ring. In another embodiment, the substituent Q is CN and is in the para position of the B ring.

[000190] As contemplated herein, when the integers m and n are greater than one, the substituents R2 and R3 are not limited to one particular substituent, and can be any combination of the substituents listed above.

[000191] In another embodiment, the SARM compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a compound of Formula II, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxid,e crystal, polymorph, prodrug or any combination thereof:

II wherein

X is a bond, O, CH ₂ , NH, Se, PR, or NR;

G is O or S;

T is OH, OR, -NHCOCH3, or NHCOR;

Z is NO2, CN, COR, COOH or CONHR; Y is I, CF ₃ , Br, Cl, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR,

COR, OCOR, 0S0 ₂ R, S0 ₂ R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C;

R is a C1-C4 alkyl, aryl, phenyl, alkenyl, hydroxyl, a C1-C4 haloalkyl, halogen, or haloalkenyl; and

Ri is CH ₃ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ .

[000192] In one embodiment, this invention relates to prescreening then treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR-positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prescreening then prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER-positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER-positive breast cancer; h) prescreening then treating a subject suffering from refractory ER-positive breast cancer; i) prescreening then treating a subject suffering from AR- positive ER-positive breast cancer; j) prescreening then treating a subject suffering from AR- positive ER-positive refractory breast cancer; k) prescreening then treating a subject suffering from AR-positive ER-positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3- kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2-positive breast cancer; u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula II: wherein

X is a bond, O, CH ₂ , NH, Se, PR, or NR;

G is O or S;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

Z is NO2, CN, COR, COOH or CONHR;

Y is I, CF ₃ , Br, Cl, or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, OSO2R, SO2R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C;

R is a C1-C4 alkyl, aryl, phenyl, alkenyl, hydroxyl, a C1-C4 haloalkyl, halogen, or haloalkenyl; and

Ri is CH ₃ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000193] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then treating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then beating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula II:

II wherein X is a bond, O, CH ₂ , NH, Se, PR, or NR;

G is O or S;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

Z is NO2, CN, COR, COOH or CONHR;

Y is I, CF ₃ , Br, Cl, or Sn(R) ₃ ; Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR,

NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C;

R is a C1-C4 alkyl, aryl, phenyl, alkenyl, hydroxyl, a C1-C4 haloalkyl, halogen, or haloalkenyl; and

Ri is CH ₃ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000194] In one embodiment, G in Formula II is O. In another embodiment, X in Formula II is O. In another embodiment, T in Formula II is OH. In another embodiment, Ri in Formula II is CH3. In another embodiment, Z in Formula II is NO2. In another embodiment, Z in Formula II is CN. In another embodiment, Y in Formula II is CF3. In another embodiment, Y in Formula II is halogen. In another embodiment, Y in Formula II is Cl. In another embodiment, Q in Formula II is CN. In another embodiment, Q in Formula II is halogen. In another embodiment, Q in Formula II is Cl. In another embodiment, Q in Formula II is F. In another embodiment, Q in Formula II is NHCOCH3. In another embodiment, Q in Formula II is in the para position. In another embodiment, Z in Formula II is in the para position. In another embodiment, Y in Formula II is in the meta position. In another embodiment, G in Formula II is O, T is OH, Ri is CH3, X is O, Z is CN, Y is CF3 or halogen and Q is CN or F. In another embodiment, G in Formula II is O, T is OH, Ri is CH ₃ , X is O, Z is N0 ₂ , Y is CF ₃ and Q is NHCOCH3, F or Cl.

[000195] The substituents Z and Y can be in any position of the ring carrying these substituents (hereinafter “A ring”). In one embodiment, the substituent Z is in the para position of the A ring. In another embodiment, the substituent Y is in the meta position of the A ring. In another embodiment, the substituent Z is in the para position of the A ring and substituent Y is in the meta position of the A ring.

[000196] The substituent Q can be in any position of the ring carrying this substituent (hereinafter “B ring”). In one embodiment, the substituent Q is in the para position of the B ring. In another embodiment, the substituent Q is CN and is in the para position of the B ring.

[000197] In another embodiment, the SARM compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR- positive refractory breast cancer; f) prescreening then treating a subject suffering from AR- positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR- positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression- free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula III, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxid,e crystal, polymorph, prodrug or any combination thereof: wherein

Z is NO2, CN, COOH, COR, NHCOR or CONHR; Y is CF ₃ , F, I, Br, Cl, CN, C(R) or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH. [000198] In one embodiment, this invention relates to prescreening then treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR-positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prescreening then prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER-positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER-positive breast cancer; h) prescreening then treating a subject suffering from refractory ER-positive breast cancer; i) prescreening then treating a subject suffering from AR- positive ER-positive breast cancer; j) prescreening then treating a subject suffering from AR- positive ER-positive refractory breast cancer; k) prescreening then treating a subject suffering from AR-positive ER-positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3- kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2-positive breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula III:

III wherein

Z is NO2, CN, COOH, COR, NHCOR or CONHR;

Y is CF ₃ , F, I, Br, Cl, CN, C(R) ₃ or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000199] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then treating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula III: wherein

Z is NO2, CN, COOH, COR, NHCOR or CONHR; Y is CF ₃ , F, I, Br, Cl, CN, C(R) ₃ or Sn(R) ₃ ;

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000200] In one embodiment, Z in Formula III is NO2. In another embodiment, Z in Formula III is CN. In another embodiment, Y in Formula III is CF3. In another embodiment, Y in Formula III is Cl. In another embodiment, Y in Formula III is halogen. In another embodiment, Q in Formula III is CN. In another embodiment, Q in Formula III is halogen. In another embodiment, Q in Formula III is F. In another embodiment, Q in Formula III is Cl. In another embodiment, Q in Formula III is NHCOCH3. In another embodiment, Z is CN, Y is CF3 or halogen, and Q is CN or F. In another embodiment, Z is NO2, Y is CF3, and Q is NHCOCH3, F or Cl.

[000201] In another embodiment, the SARM compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR- positive refractory breast cancer; f) prescreening then treating a subject suffering from AR- positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR- positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula IV, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof:

IV wherein

X is a bond, O, CH ₂ , NH, S, Se, PR, NO or NR; G is O or S;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH; A is a ring selected from: B is a ring selected from: wherein A and B cannot simultaneously be a benzene ring;

Z is NO2, CN, COOH, COR, NHCOR or CONHR;

Y is CF ₃ , F, I, Br, Cl, CN, C(R) ₃ or Sn(R) ₃ ;

Qi and Q2 are independently hydrogen, alkyl, halogen, CF ₃ , CN, C(R) ₃ , Sn(R) ₃ , N(R)2, NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHSO2R, OR, COR, OCOR, OSO2R, S0 ₂ R, SR, or

Q ₃ and Q4 are independently of each other a hydrogen, alkyl, halogen, CF ₃ , CN, C(R) ₃ , Sn(R) ₃ , N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHSO2R, OR, COR, OCOR, OSO2R, SO2R or SR;

Wi is O, NH, NR, NO or S; and W ₂ is N or NO.

[000202] In one embodiment, this invention relates to prescreening then treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR-positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prescreening then prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER-positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER-positive breast cancer; h) prescreening then treating a subject suffering from refractory ER-positive breast cancer; i) prescreening then treating a subject suffering from AR- positive ER-positive breast cancer; j) prescreening then treating a subject suffering from AR- positive ER-positive refractory breast cancer; k) prescreening then treating a subject suffering from AR-positive ER-positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3- kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2-positive breast cancer; u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula IV :

IV wherein

X is a bond, O, CH ₂ , NH, S, Se, PR, NO or NR;

G is O or S;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH;

A is a ring selected from: wherein A and B cannot simultaneously be a benzene ring; Z is N0 ₂ , CN, COOH, COR, NHCOR or CONHR;

Y is CF ₃ , F, I, Br, Cl, CN, C(R) ₃ or Sn(R) ₃ ;

Qi and Q ₂ are independently hydrogen, alkyl, halogen, CF ₃ , CN, C(R) ₃ , Sn(R) ₃ , N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCTH, NHCSCF ₃ , NHCSR, NHS0 ₂ CH ₃ , NHS0 ₂ R, OR, COR, OCOR, 0S0 ₂ R, S0 ₂ R, SR, or

Q3 and Q4 are independently of each other a hydrogen, alkyl, halogen, CF3, CN, C(R)3, Sn(R) ₃ , N(R)2, NHCOCH3, NHCOCF3, NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCOCH ₃ , NHCSCF3, NHCSR, NHSO2CH3, NHSO2R, OR, COR, OCOR, OSO2R, SO2R or SR;

Wi is O, NH, NR, NO or S; and W ₂ is N or NO; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000203] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then beating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then beating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2-positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula IV :

IV wherein

X is a bond, O, CH ₂ , NH, S, Se, PR, NO or NR; G is O or S;

Ri is CH ₃ , CH ₂ F, CHF ₂ , CF ₃ , CH ₂ CH ₃ , or CF ₂ CF ₃ ;

T is OH, OR, -NHCOCH ₃ , or NHCOR;

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH; A is a ring selected from: wherein A and B cannot simultaneously be a benzene ring; Z is N0 ₂ , CN, COOH, COR, NHCOR or CONHR;

Y is CF ₃ , F, I, Br, Cl, CN, C(R) ₃ or Sn(R) ₃ ; Qi and Q ₂ are independently hydrogen, alkyl, halogen, CF ₃ , CN, C(R) ₃ , Sn(R) ₃ , N(R) ₂ , NHCOCH3, NHCOCF3, NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH3, Q ₃ and Q ₄ are independently of each other a hydrogen, alkyl, halogen, CF ₃ , CN, C(R) ₃ ,

Sn(R) ₃ , N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHSO ₂ CH ₃ , NHSO ₂ R, OR, COR, OCOR, OSO ₂ R, SO2R or SR;

Wi is O, NH, NR, NO or S; and W ₂ is N or NO; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject. [000204] In one embodiment, G in Formula IV is O. In another embodiment, X in Formula

IV is O. In another embodiment, T in Formula IV is OH. In another embodiment, Ri in Formula IV is CH ₃ . In another embodiment, Z in Formula IV is NO ₂ . In another embodiment, Z in Formula IV is CN. In another embodiment, Y in Formula IV is CF ₃ . In another embodiment, Y in Formula IV is halogen. In another embodiment, Y in Formula IV is Cl. In another embodiment, Qi in Formula II is CN. In another embodiment, Qi in Formula IV is F. In another embodiment, Qi in Formula IV is Cl. In another embodiment, Qi in Formula II is NHCOCH ₃ . In another embodiment, Qi in Formula IV is in the para position. In another embodiment, Z in Formula IV is in the para position. In another embodiment, Y in Formula IV is in the meta position. In another embodiment, G in Formula IV is O, T is OH, Ri is CH ₃ , X is O, Z is NO ₂ or CN, Y is CF ₃ or halogen and Qi is CN, F, Cl, or NHCOCH ₃ .

[000205] The substituents Z and Y can be in any position of the ring carrying these substituents (hereinafter “A ring”). In one embodiment, the substituent Z is in the para position of the A ring. In another embodiment, the substituent Y is in the meta position of the A ring. In another embodiment, the substituent Z is in the para position of the A ring and substituent Y is in the meta position of the A ring.

[000206] The substituents Qi and Q2 can be in any position of the ring carrying these substituents (hereinafter “B ring”). In one embodiment, the substituent Qi is in the para position of the B ring. In another embodiment, the substituent is Q2 is H. In another embodiment, the substituent Qi is in the para position of the B ring and the substituent is Q2 is H. In another embodiment, the substituent Qi is CN and is in the para position of the B ring, and the substituent is Q2 is H.

[000207] As contemplated herein, other specific embodiments of compounds included within the scope of the present invention, and which are useful in: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer;, are Formula V or VI. It is understood that included within the scope of the present invention are analogs, derivatives, metabolites, isomers, pharmaceutically acceptable salts, pharmaceutical products, hydrates, N-oxides, polymorphs, crystals, prodrugs or combinations thereof of these compounds:

V or

VI wherein

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH3, NHCSCF3, NHCSR, NHSO2CH3, NHSO2R, OR, COR, OCOR, OSO2R, SO2R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

A B C; and R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH.

[000208] In one embodiment, this invention relates to prescreening then treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR-positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER-positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER-positive breast cancer; h) prescreening then treating a subject suffering from refractory ER-positive breast cancer; i) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer; j) prescreening then treating a subject suffering from AR-positive ER-positive refractory breast cancer; k) prescreening then treating a subject suffering from AR-positive ER- positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR- positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2-positive breast cancer; u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer , comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by the following structures of Formula V or VI:

V or

VI wherein

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH3, NHCSCF3, NHCSR, NHSO2CH3, NHSO2R, OR, COR, OCOR, OSO2R, SO2R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH2F, CHF2, CF ₃ , CF2CF ₃ , aryl, phenyl, halogen, alkenyl or OH; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject. [000209] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then treating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula V or VI:

V or

VI wherein

Q is CN, alkyl, halogen, N(R) ₂ , NHCOCH ₃ , NHCOCF ₃ , NHCOR, NHCONHR, NHCOOR, OCONHR, CONHR, NHCSCH ₃ , NHCSCF ₃ , NHCSR, NHSO ₂ CH ₃ , NHSO ₂ R, OR, COR, OCOR, OSO2R, SO2R or SR; or Q together with the benzene ring to which it is attached is a fused ring system represented by structure A, B or C:

R is alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH ₂ F, CHF ₂ , CF ₃ , CF ₂ CF ₃ , aryl, phenyl, halogen, alkenyl or OH; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000210] In one embodiment, Q in Formula V or VI is CN. In one embodiment, Q in Formula V or VI is halogen. In one embodiment, Q in Formula V or VI is F. In one embodiment, Q in Formula V or VI is Cl. In one embodiment, Q in Formula V or VI is NHCOCH ₃ .

[000211] In another embodiment, the SARM compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR- positive refractory breast cancer; f) prescreening then treating a subject suffering from AR- positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR- positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula VII, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof:

VII wherein Z is Cl or CF3.

[000212] In one embodiment, this invention relates to prescreening and treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR- positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prescreening then prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER- positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER- positive breast cancer; h) prescreening then treating a subject suffering from refractory ER- positive breast cancer; i) prescreening then treating a subject suffering from AR-positive ER- positive breast cancer; j) prescreening then treating a subject suffering from AR-positive ER- positive refractory breast cancer; k) prescreening then treating a subject suffering from AR- positive ER-positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatment with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PBKa)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2-positive breast cancer; and/or u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by the following structures of Formula VII:

VII wherein Z is Cl or CF3; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject

[000213] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then beating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then beating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by a compound of Formula VII:

VII wherein Z is Cl or CF3; and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000214] In another embodiment, the compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula VIII, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof:

[000215] In another embodiment, the compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula K, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxid,e crystal, polymorph, prodrug or any combination thereof:

IX. [000216] In another embodiment, the compound as descried herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3- kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula X, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof:

[000217] In another embodiment, the compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula XI, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxid,e crystal, polymorph, prodrug or any combination thereof:

XI.

[000218] In another embodiment, the compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula XII, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxid,e crystal, polymorph, prodrug or any combination thereof: [000219] In another embodiment, the compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a compound of Formula XIII, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof:

XIII.

[000220] In another embodiment, the compound as described herein, which is effective at: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening thenslowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, is a compound represented by a structure of Formula XIV, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof:

XIV.

[000221] In one embodiment, this invention relates to prescreening then treatment of androgen receptor-positive breast cancer in a subject, for example a female subject. Accordingly, this invention provides methods for: a) prescreening then treating AR-positive breast cancer in a subject; b) prescreening then treating metastatic AR-positive breast cancer, or advanced AR-positive breast cancer; c) prescreening then treating refractory AR-positive breast cancer; d) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; e) prescreening then prolonging progression-free survival of a subject suffering from breast cancer; f) prescreening then treating a subject suffering from ER-positive breast cancer; g) prescreening then treating a subject suffering from metastatic ER-positive breast cancer; h) prescreening then treating a subject suffering from refractory ER-positive breast cancer; i) prescreening then treating a subject suffering from AR- positive ER-positive breast cancer; j) prescreening then treating a subject suffering from AR- positive ER-positive refractory breast cancer; k) prescreening then treating a subject suffering from AR-positive ER-positive metastatic breast cancer; 1) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; m) prescreening then treating a subject suffering from AR-positive ER-positive breast cancer with or without expression of PR, and/or HER2; n) prescreening then treating a subject suffering from advanced ER-positive breast cancer; o) prescreening then treating a subject suffering from ER-positive breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3- kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; p) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from ER-positive breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; and/or t) prescreening then treating a subject suffering from AR-positive HER2 -positive breast cancer; u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by the following structures of Formulae VIII, IX, X, XI, XII, XIII and XIV:

XIII; and

XIV and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000222] In another embodiment, this invention provides methods for: a) prescreening then treating a subject suffering from HER2 -positive breast cancer; b) prescreening then treating a subject suffering from HER2 -positive refractory breast cancer; c) prescreening then treating a subject suffering from HER2 -positive metastatic breast cancer; d) prescreening then treating a subject suffering from HER2 -positive and ER-negative breast cancer; e) prescreening then treating a subject suffering from HER2 -positive and ER-positive breast cancer; f) prescreening then treating a subject suffering from HER2-positive and PR-positive breast cancer; g) prescreening then treating a subject suffering from HER2-positive and PR-negative breast cancer; h) prescreening then treating a subject suffering from HER2-positive and AR-positive breast cancer; i) prescreening then treating a subject suffering from HER2 -positive and AR- negative breast cancer; j) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-positive, and AR-positive breast cancer; k) prescreening then treating a subject suffering from HER2 -positive, ER-positive, PR-negative, and AR-positive breast cancer; 1) prescreening then treating a subject suffering from HER2-positive, ER-positive, PR- negative, and AR-negative breast cancer; m) prescreening then treating a subject suffering from HER2- positive, ER-positive, PR-positive, and AR-negative breast cancer; n) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-negative, and AR-positive breast cancer; o) prescreening then treating a subject suffering from HER2 -positive, ER- negative, PR-positive, and AR-positive breast cancer; p) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR-positive, and AR-negative breast cancer; and/or q) prescreening then treating a subject suffering from HER2 -positive, ER-negative, PR- negative, and AR-negative breast cancer; comprising administering to the subject a therapeutically effective amount of a selective androgen receptor modulator (SARM) compound represented by the following structures of Formulae VIII, IX, X, XI, XII, XIII and XIV:

XII;

XIV and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein. In one embodiment, the subject is a female subject. In one embodiment, the subject is a male subject.

[000223] In one embodiment, the methods of this invention make use of a compound of Formula VIII. In one embodiment, the methods of this invention make use of a compound of

Formula IX. In one embodiment, the methods of this invention make use of a compound of

Formula X. In one embodiment, the methods of this invention make use of a compound of

Formula XI. In one embodiment, the methods of this invention make use of a compound of

Formula XII. In one embodiment, the methods of this invention make use of a compound of Formula XIII. In one embodiment, the methods of this invention make use of a compound of

Formula XIV.

[000224] In one embodiment, the methods of the present invention comprise administering an analog of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a derivative of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering an isomer of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a metabolite of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a pharmaceutically acceptable salt of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a pharmaceutical product of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a hydrate of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering an N-oxide of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a polymorph of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a crystal of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a prodrug of the compound of Formulae I-XIV. In another embodiment, the methods of the present invention comprise administering a combination of any of an analog, derivative, metabolite, isomer, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N- oxide, polymorph, crystal or prodrug of the compound of Formulae I-XIV.

[000225] In one embodiment, the methods of this invention comprise administering a compound of Formulae I-XIV. In another embodiment, the methods of this invention comprise administering a compound of Formula I. In another embodiment, the methods of this invention comprise administering a compound of Formula II. In another embodiment, the methods of this invention comprise administering a compound of Formula III. In another embodiment, the methods of this invention comprise administering a compound of Formula IV. In another embodiment, the methods of this invention comprise administering a compound of Formula V. In another embodiment, the methods of this invention comprise administering a compound of Formula VI. In another embodiment, the methods of this invention comprise administering a compound of Formula VII. In another embodiment, the methods of this invention comprise administering a compound of Formula VIII. In another embodiment, the methods of this invention comprise administering a compound of Formula IX. In another embodiment, the methods of this invention comprise administering a compound of Formula X. In another embodiment, the methods of this invention comprise administering a compound of Formula XI. In another embodiment, the methods of this invention comprise administering a compound of Formula XII. In another embodiment, the methods of this invention comprise administering a compound of Formula XIII. In another embodiment, the methods of this invention comprise administering a compound of Formula XIV.

[000226] The compounds as described herein, either alone or as in a pharmaceutical composition, are useful for: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then beating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado- bastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then prolonging survival of a subject with ER-positive breast cancer; r) prescreening then slowing the progression of ER-positive breast cancer in a subject; s) prescreening then prolonging progression-free survival of a subject with ER-positive breast cancer; t) prescreening then treating a subject suffering from AR-positive HER2 -positive breast cancer, u) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or v) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer.

[000227] The compounds as described herein offer a significant advantage over steroidal androgen treatment since treatment of breast cancer with these compounds will not be accompanied by serious side effects, inconvenient modes of administration, or high costs and still have the advantages of oral bioavailability, lack of cross-reactivity with other steroid receptors, lack of aromatizability, and long biological half-lives.

[000228] In one embodiment, this invention relates to prescreening then treatment of androgen receptor-positive breast cancer in a subject. Accordingly, this invention provides methods of: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR- positive refractory breast cancer; f) prescreening then treating a subject suffering from AR- positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR- positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating a subject suffering from HER2 -positive breast cancer; r) prescreening then treating a subject suffering from ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer, by administering to the subject a therapeutically effective amount of a selective androgen receptor modulator of Formulae I-XIV as described herein, and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, as described herein.

[000229] As defined herein, the term “isomer” includes, but is not limited to, optical isomers and analogs, structural isomers and analogs, conformational isomers and analogs, and the like. As used herein, the term "isomer" may also be referred to herein as an "enantiomer" having all of the qualities and properties of an "isomer".

[000230] In one embodiment, this invention encompasses the use of various optical isomers of the selective androgen receptor modulator. It will be appreciated by those skilled in the art that the selective androgen receptor modulators of Formulae I-XIV as described hereincontain at least one chiral center. Accordingly, the selective androgen receptor modulators used in the methods of the present invention may exist in, and be isolated in, optically-active or racemic forms. Some compounds may also exhibit polymorphism. It is to be understood that the present invention encompasses any racemic, optically-active, polymorphic, or stereoisomeric form, or any combination thereof, which form possesses properties useful in the treatment of androgen- related conditions described herein. In one embodiment, the selective androgen receptor modulators are the pure (R)-isomers. In another embodiment, the selective androgen receptor modulators are the pure (5)-isomers. In another embodiment, the selective androgen receptor modulators are a mixture of the ( R ) and the ( S ) isomers. In another embodiment, the selective androgen receptor modulators are a racemic mixture comprising an equal amount of the (R) and the (S) isomers. It is well known in the art how to prepare optically-active forms (for example, by resolution of the racemic form by recrystallization techniques, by synthesis from optically- active starting materials, by chiral synthesis, or by chromatographic separation using a chiral stationary phase).

[000231] The invention includes uses of “pharmaceutically acceptable salts” of the SARM compounds as described herein, which may be produced, by reaction of a SARM compound of Formulae I-XIV as described herein with an acid or base.

[000232] The invention includes uses of pharmaceutically acceptable salts of amino- substituted compounds with organic and inorganic acids, for example, citric acid and hydrochloric acid. The invention also includes N-oxides of the amino substituents of the compounds described herein. Pharmaceutically acceptable salts can also be prepared from the phenolic compounds by treatment with inorganic bases, for example, sodium hydroxide. Also, esters of the phenolic compounds can be made with aliphatic and aromatic carboxylic acids, for example, acetic acid and benzoic acid esters.

[000233] Suitable pharmaceutically acceptable salts of the compounds of Formulae I-XIV may be prepared from an inorganic acid or from an organic acid. In one embodiment, examples of inorganic salts of the SARM compounds as described herein are bisulfates, borates, bromides, chlorides, hemisulfates, hydrobromates, hydrochlorates, 2-hydroxy ethylsulfonates (hydroxyethanesulfonates), iodates, iodides, isothionates, nitrates, persulfates, phosphate, sulfates, sulfamates, sulfanilates, sulfonic acids (alkylsulfonates, arylsulfonates, halogen substituted alkylsulfonates, halogen substituted arylsulfonates), sulfonates and thiocyanates.

[000234] In one embodiment, examples of organic salts of the SARM compounds as described herein may be selected from aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, examples of which are acetates, arginines, aspartates, ascorbates, adipates, anthranilates, algenates, alkane carboxylates, substituted alkane carboxylates, alginates, benzenesulfonates, benzoates, bisulfates, butyrates, bicarbonates, bitartrates, citrates, camphorates, camphorsulfonates, cyclohexylsulfamates, cyclopentanepropionates, calcium edetates, camsylates, carbonates, clavulanates, cinnamates, dicarboxylates, digluconates, dodecylsulfonates, dihydrochlorides, decanoates, enanthuates, ethanesulfonates, edetates, edisylates, estolates, esylates, fumarates, formates, fluorides, galacturonates gluconates, glutamates, glycolates, glucorate, glucoheptanoates, glycerophosphates, gluceptates, glycollylarsanilates, glutarates, glutamate, heptanoates, hexanoates, hydroxymaleates, hydroxycarboxlic acids, hexylresorcinates, hydroxybenzoates, hydroxynaphthoate, hydrofluorate, lactates, lactobionates, laurates, malates, maleates, methylenebis(beta-oxynaphthoate), malonates, mandelates, mesylates, methane sulfonates, methylbromides, methylnitrates, methylsulfonates, monopotassium maleates, mucates, monocarboxylates, nitrates, naphthalenesulfonates, 2-naphthalenesulfonates, nicotinates, napsylates, N- m el h y 1 g 1 u c a m i n es , oxalates, octanoates, oleates, pamoates, phenylacetates, picrates, phenylbenzoates, pivalates, propionates, phthalates, phenylacetate, pectinates, phenylpropionates, palmitates, pantothenates, polygalacturates, pyruvates, quinates, salicylates, succinates, stearates, sulfanilate, subacetates, tartrates, theophyllineacetates, p- toluenesulfonates (tosylates), trifluoroacetates, terephthalates, tannates, teoclates, trihaloacetates, triethiodide, tricarboxylates, undecanoates and valerates.

[000235] In one embodiment, the salts may be formed by conventional means, such as by reacting the free base or free acid form of the product with one or more equivalents of the appropriate acid or base in a solvent or medium in which the salt is insoluble or in a solvent such as water, which is removed in vacuo or by freeze drying or by exchanging the ions of an existing salt for another ion or suitable ion-exchange resin.

[000236] This invention further includes derivatives of the selective androgen receptor modulators. The term “derivatives” includes but is not limited to ether derivatives, acid derivatives, amide derivatives, ester derivatives and the like. In addition, this invention further includes hydrates of the selective androgen receptor modulators. The term “hydrate” includes but is not limited to hemihydrate, monohydrate, dihydrate, trihydrate and the like.

[000237] This invention further includes uses of metabolites of the selective androgen receptor modulators. The term “metabolite” means any substance produced from another substance by metabolism or a metabolic process.

[000238] This invention further includes uses of pharmaceutical products of the selective androgen receptor modulators. The term “pharmaceutical product” means a composition suitable for pharmaceutical use (pharmaceutical composition), as defined herein.

[000239] This invention further includes uses of prodrugs of the selective androgen receptor modulators. The term “prodrug” means a substance which can be converted in vivo into a biologically active agent by such reactions as hydrolysis, esterification, de-esterification, activation, salt formation and the like.

[000240] This invention further includes uses of crystals of the selective androgen receptor modulators. Furthermore, this invention provides polymorphs of the selective androgen receptor modulators. The term “crystal” means a substance in a crystalline state. The term “polymorph” refers to a particular crystalline state of a substance, having particular physical properties such as X-ray diffraction, IR spectra, melting point, and the like.

[000241] In one embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as describe herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000242] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from metastatic breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000243] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from refractory breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat refractory breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000244] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000245] In one embodiment, the AR-positive breast cancer is ER, PR and HER2 -positive. In another embodiment, the AR-positive breast cancer is ER, PR and HER2-negative. In one embodiment, the AR-positive breast cancer is ER-positive, and PR and HER2-negative. In another embodiment, the AR-positive breast cancer is ER and PR-positive, and HER2-negative. In yet another embodiment, the AR-positive breast cancer is ER and HER2 -positive, and PR- negative. In still another embodiment, the AR-positive breast cancer is ER-negative, and PR and HER2 -positive. In a further embodiment, the AR-positive breast cancer is ER and PR- negative, and HER2-positive. In still a further embodiment, the AR-positive breast cancer is ER and HER2-negative, and PR-positive. In one embodiment, the AR-positive breast cancer is ER-negative. In another embodiment, the AR-positive breast cancer is ER-positive.

[000246] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive refractory breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive refractory breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject. [000247] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive metastatic breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000248] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from ER-positive breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat ER-positive breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000249] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000250] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from ER-positive refractory breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat ER-positive refractory breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000251] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from ER-positive metastatic breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat ER-positive metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject. [000252] In one embodiment, an ER-positive breast cancer is AR-positive. In another embodiment, an ER-positive breast cancer is AR-negative.

[000253] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from advanced breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat advanced breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject. [000254] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive and ER-positive refractory breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000255] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from AR-positive and ER-negative breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat AR-positive and ER-negative metastatic breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000256] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from triple negative breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat triple negative breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000257] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000258] In another embodiment of the present invention, a method is provided for prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat, prevent, suppress or inhibit metastasis in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000259] In another embodiment of the present invention, a method is further provided for treating and/or preventing skeletal related events in a subject suffering, comprising the step of administering to the subject a selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat and/or prevent skeletal related events in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000260] In another embodiment of the present invention, a method is provided for prescreening then and treating a subject suffering from HER2-positive breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV of this invention and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat HER2-positive breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000261] In one embodiment, the HER2-positive breast cancer is HER2 -positive refractory breast cancer. In another embodiment, the HER2 -positive breast cancer is HER2 -positive metastatic breast cancer. In one embodiment, the HER2 -positive breast cancer is ER-negative. In another embodiment, the HER2 -positive breast cancer is ER-positive. In one embodiment, the HER2-positive breast cancer is PR-positive. In another embodiment, the HER2-positive breast cancer is PR-negative. In one embodiment, the HER2 -positive breast cancer is AR- positive. In another embodiment, the HER2 -positive breast cancer is AR-negative.

[000262] In certain embodiment, the HER2-positive breast cancer is ER-positive, PR- positive, and AR-positive. In another embodiment, the HER2-positive breast cancer is ER- positive, PR-negative, and AR-positive. In another embodiment, the HER2 -positive breast cancer is ER-positive, PR-negative, and AR-negative. In another embodiment, the HER2- positive breast cancer is ER-positive, PR-positive, and AR-negative. In another embodiment, the HER2-positive breast cancer is ER-negative, PR-negative, and AR-positive. In another embodiment, the HER2 -positive breast cancer is ER-negative, PR-positive, and AR-positive. In other embodiment, the HER2 -positive breast cancer is ER-negative, PR-positive, and AR- negative. In certain embodiment, the HER2-positive breast cancer is ER-negative, PR- negative, and AR-negative. [000263] In another embodiment of the present invention, a method is provided for prescreening then treating a subject suffering from ER mutant expressing breast cancer, comprising the step of administering to the subject a compound of Formulae I-XIV of this invention and/or its analog, derivative, isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, hydrate, N-oxide, crystal, polymorph, prodrug or any combination thereof, in an amount effective to treat ER mutant expressing breast cancer in the subject. In one embodiment, the subject is a female subject. In another embodiment, the subject is a male subject.

[000264] In certain embodiment, the ER mutant expressing breast cancer is Y537S mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is D351Y mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is E380Q mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is V422del mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is S432L mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is G442A mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is S463P mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L469V mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536R mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536H mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536P mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is L536Q mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is Y537N mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is Y537C mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is Y537D mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is D538G mutation expressing breast cancer. In a certain embodiment, the ER mutant expressing breast cancer is E542G mutation expressing breast cancer. In one embodiment, ER mutant expressing breast cancer refers to mutants of ER- alpha.

[000265] In a certain embodiment, the ER mutant expressing breast cancer is as described in Cancer Cell 2018, 33, 173-186, or in Nat Rev Cancer. 2018 Jun;18(6):377-388, which are incorporated herein by reference. In one embodiment, ER mutant expressing breast cancer refers to mutants of ER-alpha.

[000266] The substituent R is defined herein as an alkyl, haloalkyl, dihaloalkyl, trihaloalkyl, CH2F, CHF2, CF3, CF2CF3; aryl, phenyl, halogen, alkenyl, or hydroxyl (OH). [000267] An “alkyl” group refers to a saturated aliphatic hydrocarbon, including straight- chain, branched-chain and cyclic alkyl groups. In one embodiment, the alkyl group has 1-12 carbons. In another embodiment, the alkyl group has 1-7 carbons. In another embodiment, the alkyl group has 1-6 carbons. In another embodiment, the alkyl group has 1-4 carbons. The alkyl group may be unsubstituted or substituted by one or more groups selected from halogen, hydroxy, alkoxy carbonyl, amido, alkylamido, dialkylamido, nitro, amino, alkylamino, dialkylamino, carboxyl, thio and thioalkyl.

[000268] A “haloalkyl” group refers to an alkyl group as defined above, which is substituted by one or more halogen atoms, e.g., by F, Cl, Br or I.

[000269] An “aryl” group refers to an aromatic group having at least one carbocyclic aromatic group or heterocyclic aromatic group, which may be unsubstituted or substituted by one or more groups selected from halogen, haloalkyl, hydroxy, alkoxy carbonyl, amido, alkylamido, dialkylamido, nitro, amino, alkylamino, dialkylamino, carboxy or thio or thioalkyl. Nonlimiting examples of aryl rings are phenyl, naphthyl, pyranyl, pyrrolyl, pyrazinyl, pyrimidinyl, pyrazolyl, pyridinyl, furanyl, thiophenyl, thiazolyl, imidazolyl, isoxazolyl, and the like. [000270] A “hydroxyl” group refers to an OH group. An “alkenyl” group refers to a group having at least one carbon to carbon double bond. A halo group refers to F, Cl, Br or I.

[000271] An “arylalkyl” group refers to an alkyl bound to an aryl, wherein alkyl and aryl are as defined above. An example of an aralkyl group is a benzyl group.

Biological Activity of Selective Androgen Receptor Modulators [000272] The selective androgen receptor modulators provided herein are a new class of compounds, which suppress growth of AR-positive breast cancers. The SARM compounds as described herein have a tissue-selective myoanabolic activity profile of a nonsteroidal ligand for the androgen receptor. Furthermore, the SARM compounds as described herein are non- aromatizable, non-virilizing, and are not commonly cross-reactive with ER and PR. In addition, in one embodiment, the selective androgen receptor modulators (SARMs) as described herein are beneficial to refractory breast cancer patients undergoing chemotherapy due to anabolism.

[000273] As contemplated herein, the appropriately substituted selective androgen receptor modulators of Formulae I-XIV as described herein are useful for: a) prescreening then treating a subject suffering from breast cancer; b) prescreening then treating a subject suffering from metastatic breast cancer; c) prescreening then treating a subject suffering from refractory breast cancer; d) prescreening then treating a subject suffering from AR-positive breast cancer; e) prescreening then treating a subject suffering from AR-positive refractory breast cancer; f) prescreening then treating a subject suffering from AR-positive metastatic breast cancer; g) prescreening then treating a subject suffering from AR-positive and ER-positive breast cancer; h) prescreening then treating a subject suffering from AR-positive breast cancer with or without expression of ER, PR, and/or HER2; i) prescreening then treating a subject suffering from triple negative breast cancer; j) prescreening then treating a subject suffering from advanced breast cancer; k) prescreening then treating a subject suffering from breast cancer that has failed treatments with selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3-kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab- cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan- nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof; 1) prescreening then treating a subject suffering from ER-positive breast cancer; m) prescreening then treating, preventing, suppressing or inhibiting metastasis in a subject suffering from breast cancer; n) prescreening then prolonging survival of a subject with breast cancer; o) prescreening then slowing the progression of breast cancer in a subject; p) prescreening then prolonging progression-free survival of a subject with breast cancer; q) prescreening then treating HER2-positive breast cancer; r) prescreening then treating ER mutant expressing breast cancer, and/or s) prescreening then treating a subject suffering from Y537S ER mutant expressing breast cancer.

[000274] In one embodiment, a “refractory breast cancer” is a breast cancer that has not responded to treatment. In another embodiment, a “refractory breast cancer” is a breast cancer resistant to treatment. In one embodiment, refractory breast cancer is refractory metastatic breast cancer. In one embodiment, refractory breast cancer has not responded to treatment with anthracy clines, taxanes, capecitabine, ixabepilone, selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof or any combination thereof.

[000275] In one embodiment, a “triple negative breast cancer” is defined by lack of expression of estrogen, progesterone, and ErbB2 (also known as human epidermal growth factor receptor 2 (HER2)) receptors. This subgroup accounts for 15% of all types of breast cancer. This subtype of breast cancer is clinically characterized as more aggressive and less responsive to standard treatment and associated with poorer overall patient prognosis.

[000276] In one embodiment, the methods of this invention are directed to prescreening then treating a subject suffering from AR-positive breast cancer, regardless of grade, stage or prior treatments.

[000277] In one embodiment, the methods of this invention are directed to prescreening then treating a subject suffering from HER2-positive breast cancer, regardless of grade, stage or prior treatments.

[000278] In one embodiment, the methods of this invention are first, second, third, or fourth line therapies for breast cancer. A first line therapy refers to a medical therapy recommended for the initial treatment of a disease, sign or symptom. A second line therapy therapy is given when initial treatment (first-line therapy) does not work, or stops working. Third line therapy is given when both initial treatment (first-line therapy) and subsequent treatment (second-line therapy) does not work, or stop working, etc.

[000279] As used herein, “kinases” are a group of enzymes that catalyze the transfer of a phosphate group from a donor, such as ADP or ATP, to an acceptor. In one embodiment, phosphorylation results in a functional change of the target protein (substrate) by changing enzyme activity, cellular location, or association with other protein kinases. Kinases regulate the majority of cellular pathways, especially those involved in signal transduction. In one embodiment, deregulated kinase activity is a frequent cause of disease, in particular cancer, wherein kinases regulate many aspects that control cell growth, movement and death. In one embodiment, drugs that inhibit specific kinases are used to treat kinase-related diseases, including cancer. In one embodiment, HER2-positive breast cancers are susceptible to HER2 kinase inhibitors (e.g., trastuzumab and lapatinib) and are generally used in metastatic disease. However, some breast cancers are refractory to HER2 kinase inhibitor treatment.

[000280] As used herein, receptors for extracellular signaling molecules are collectively referred to as "cell signaling receptors". Many cell signaling receptors are transmembrane proteins on a cell surface; when they bind an extracellular signaling molecule (i.e., a ligand), they become activated so as to generate a cascade of intracellular signals that alter the behavior of the cell. In contrast, in some cases, the receptors are inside the cell and the signaling ligand has to enter the cell to activate them; these signaling molecules therefore must be sufficiently small and hydrophobic to diffuse across the plasma membrane of the cell. [000281] Steroid hormones are one example of small hydrophobic molecules that diffuse directly across the plasma membrane of target cells and bind to intracellular cell signaling receptors. These receptors are structurally related and constitute the intracellular receptor superfamily (or steroid-hormone receptor superfamily). Steroid hormone receptors include but are not limited to progesterone receptors, estrogen receptors, androgen receptors, glucocorticoid receptors, and mineralocorticoid receptors. In one embodiment, the present invention is directed to androgen receptors. In one embodiment, the present invention is directed to androgen receptor agonists. In one embodiment, the present invention is directed to progesterone receptors. In one embodiment, the present invention is directed to progesterone receptor antagonists.

[000282] In addition to ligand binding to the receptors, the receptors can be blocked to prevent ligand binding. When a substance binds to a receptor, the three-dimensional structure of the substance fits into a space created by the three-dimensional structure of the receptor in a ball and socket configuration. The better the ball fits into the socket, the more tightly it is held. This phenomenon is called affinity. If the affinity of a substance is greater than the original hormone, it will compete with the hormone and bind the binding site more frequently. Once bound, signals may be sent through the receptor into the cells, causing the cell to respond in some fashion. This is called activation. On activation, the activated receptor then directly regulates the transcription of specific genes. But the substance and the receptor may have certain attributes, other than affinity, in order to activate the cell. Chemical bonds between atoms of the substance and the atoms of the receptors may form. In some cases, this leads to a change in the configuration of the receptor, which is enough to begin the activation process (called signal transduction).

[000283] In one embodiment, the SARM compounds as described herein inhibit the intratumoral expression of genes and pathways that promote breast cancer development through their actions on the AR. In one embodiment, a SARM compound of Formulae I-XIV as described herein inhibits intratumoral expression of Muc 1 , SLUG, VCAM1 , SPARC or MMP2, or any combination thereof. In another embodiment, Formula VIII inhibits gene expression that promotes breast cancer.

[000284] In one embodiment, a receptor antagonist is a substance which binds receptors and inactivates them. In one embodiment, a selective androgen receptor modulator is a molecule that exhibits in vivo tissue selectivity, activating signaling activity of the androgen receptor (AR) in anabolic (muscle, bone, etc.) tissues to a greater extent than in the androgenic tissues. Thus, in one embodiment, the selective androgen receptor modulators of Formulae I-XIV as described herein are useful in binding to and activating steroidal hormone receptors. In one embodiment, the SARM compound as described herein is an agonist which binds the androgen receptor. In another embodiment, the compound has high affinity for the androgen receptor.

[000285] Assays to determine whether the compounds of the present invention are AR agonists or antagonists are well known to a person skilled in the art. For example, AR agonistic activity can be determined by monitoring the ability of the selective androgen receptor modulators to maintain and/or stimulate the growth of AR containing androgenic tissue such as prostate and seminal vesicles, as measured by weight, in castrated animals. AR antagonistic activity can be determined by monitoring the ability of the selective androgen receptor modulators to inhibit the growth of AR containing tissue in intact animals or counter the effects of testosterone in castrated animals.

[000286] An androgen receptor (AR) is an androgen receptor of any species, for example a mammal. In one embodiment, the androgen receptor is an androgen receptor of a human. Thus, in another embodiment, the selective androgen receptor modulators bind reversibly to an androgen receptor of a human. In another embodiment, the selective androgen receptor modulators bind reversibly to an androgen receptor of a mammal.

[000287] As contemplated herein, the term “selective androgen receptor modulator” (SARM) refers to, in one embodiment, a molecule that exhibits in vivo tissue selectivity, activating signaling activity of the androgen receptor in anabolic (muscle, bone, etc.) tissues to a greater extent than in the androgenic tissues. In another embodiment, a selective androgen receptor modulator selectively binds the androgen receptor. In another embodiment, a selective androgen receptor modulator selectively affects signaling through the androgen receptor. In one embodiment, the SARM is a partial agonist. In one embodiment, the SARM is a tissue- selective agonist, or in some embodiments, a tissue-selective antagonist.

[000288] In one embodiment, a SARM of this invention exerts its effects on the androgen receptor in a tissue-dependent manner. In one embodiment, a SARM of this invention will have an IC50 or EC50 with respect to AR, as determined using AR transactivation assays, as known in the art, or, in other embodiments, as described herein. [000289] The term “IC50” refers, in some embodiments, to a concentration of the SARM which reduces the activity of a target (e.g., AR) to half- maximal level.

[000290] The term “EC50” refers, in some embodiments, to a concentration of the SARM that produces a half-maximal effect. [000291] For example, utilizing transactivation assays, Figure 5 shows that SARM compounds as described herein exhibit AR agonist activity in MDA-MB-231 cells transfected with AR.

[000292] As defined herein, “contacting" means that the selective androgen receptor modulators of Formulae I-XIV as described herein are introduced into a sample containing the receptor in a test tube, flask, tissue culture, chip, array, plate, microplate, capillary, or the like, and incubated at a temperature and time sufficient to permit binding of the selective androgen receptor modulators to the receptor. Methods for contacting the samples with the selective androgen receptor modulators or other specific binding components are known to those skilled in the art and may be selected depending on the type of assay protocol to be ran. Incubation methods are also standard and are known to those skilled in the art.

[000293] In another embodiment, the term “contacting” means that the selective androgen receptor modulators of Formulae I-XIV as described herein are introduced into a subject receiving treatment, and the selective androgen receptor modulator is allowed to come in contact with the androgen receptor in vivo. [000294] As used herein, in some embodiments, the term “prescreening” or “prescreen” refers to analyzing a biological sample obtained from a patient and identifying or selecting said patient, including participants in clinical trials, to assess the patient's responses to a treatment prior to giving the treatment. In some embodiments, the prescreening is performed to identify or select patients as candidates for selective androgen receptor modulator (SARM) treatment. In some embodiments, the prescreening is based on the measurement prior to treatment of the percentage of androgen receptor (AR) staining. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 2%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 5%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 10%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 15%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 20%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 25%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 30%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 40%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 45%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 50%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 55%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 60%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 65%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 70%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 75%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 80%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 85%. In some embodiments, the prescreening identifies or selects patients as candidates for selective androgen receptor modulator (SARM) treatment if the percent of AR staining is greater than or equal to 90%. The terms “prescreening” and “prescreen” are used herein interchangeably.

[000295] As used herein, the term “treating” includes disorder remitative treatment. As used herein, the terms “reducing”, “suppressing” and “inhibiting” have their commonly understood meaning of lessening or decreasing. As used herein, the term “progression” means increasing in scope or severity, advancing, growing or becoming worse. As used herein, the term “recurrence” means the return of a disease after a remission. As used herein, the term “delaying” means stopping, hindering, slowing down, postponing, holding up or setting back. As used herein, the term “metastasis” refers to the transfer of a disease from one organ or part thereof to another not directly connected with it. Metastasis can occur for example as a result of transfer of malignant cells from one organ (for example breast) to other organs.

[000296] In one embodiment, "treating" refers to reducing tumor growth by 75%, as demonstrated in, e.g., Example 8. In another embodiment, treating refers to reducing tumor growth by at least 75%. In another embodiment, treating refers to reducing tumor growth by at least 50%. In another embodiment, treating refers to reducing tumor growth by at least 25%. In another embodiment, treating refers to reducing tumor growth by 50-100%. In another embodiment, treating refers to reducing tumor growth by 70-80%. In another embodiment, treating refers to reducing tumor growth by 25-125%.

[000297] In another embodiment, "treating" refers to reducing tumor weight by 50%, as demonstrated in, e.g., Example 8. In another embodiment, treating refers to reducing tumor weight by at least 50%. In another embodiment, treating refers to reducing tumor weight by at least 40%. In another embodiment, treating refers to reducing tumor weight by at least 30%. In another embodiment, treating refers to reducing tumor weight by at least 20%. In another embodiment, treating refers to reducing tumor weight by 25-75%. In another embodiment, treating refers to reducing tumor weight by 25-100%.

[000298] As used herein, the term “administering” refers to bringing a subject in contact with a compound as described herein. As used herein, administration can be accomplished in vitro, i.e., in a test tube, or in vivo, i.e., in cells or tissues of living organisms, for example humans. In one embodiment, the present invention encompasses administering the compounds of the present invention to a subject.

[000299] In one embodiment, a compound of Formulae I-XIV as described herein is administered to a subject once a week. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject twice a week. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject three times a week. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject four times a week. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject five times a week. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject daily. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject weekly. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject bi-weekly. In another embodiment, a compound of Formulae I-XIV as described herein is administered to a subject monthly.

[000300] In one embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator as the sole active ingredient. However, also encompassed within the scope of the present invention are methods for treating breast cancer, for delaying the progression of breast cancer, and for preventing and treating the recurrence of breast cancer and/or breast cancer metastasis, which comprise administering the selective androgen receptor modulators in combination with one or more therapeutic agents. These agents include, but are not limited to: selective estrogen receptor modulator (SERM) (tamoxifen, toremifene, raloxifene), gonadotropin-releasing hormone (GnRH) agonist (goserelin), aromatase inhibitor (AI) (letrozole, anastrozole, exemestane), fulvestrant, cyclin- dependent kinase 4/6 (CDK 4/6) inhibitor (palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Vorzenio), trilaciclib, lerociclib), alpelisib (Piqray) (an inhibitor of phosphatidylinositol-3 -kinase subunit alpha (PI3Ka)), mTOR inhibitor (everolimus), poly ADP ribose polymerase (PARP) inhibitor (olaparib (Lynparza) or talazoparib (Talzenna)), human epidermal growth factor receptor 2 (HER2) kinase inhibitor (lapatinib, neratinib (Nerlynx), dacomitinib (Vizimpro), or tucatinib (Tukysa)), HER2 antibody (trastuzumab (Herceptin), pertuzumab (Perjeta), margetuximab-cmkb (Margenza)), HER2 antibody drug conjugate (HER2 ADC) (am-trastuzumab-deruxtecan-nxki (Enhertu), ado-trastuzumab emtansine (Kadcyla), or pertuzumab/ trastuzumab/hyaluronidase-zzxf (Phesgo)), atezolizumab (Tecentriq) (PD-L1 blocking antibody), pembrolizumab (Keytruda) (PD-L1 blocking antibody), sacituzumab govitecan (Trodelvy) (antibody drug conjugate for TNBC), bevacizumab (Avastin), and/or sabizabulin or a pharmaceutically acceptable salt thereof, HDAC inhibitors (entinostat), PI3K inhibitors (buparlisib, tapelisib, alpelisib), vaccines and immune stimulants or adjuvants (NeuVax®), CTLA-4 (cytotoxic T-lymphocyte associated protein-4) inhibitors (tramelimumab), PD-1 inhibitors (pembrolizumab), PD-L1 inhibitors (atezolizumb, avelumab, durvalumab), chemotherapeutic agents, taxanes, anthracyclines, epothilones, LHRH analogs, reversible antiandrogens, antiestrogens, anticancer drugs, 5-alpha reductase inhibitors, progestins, agents acting through other nuclear hormone receptors such as progesterone and estrogen receptors, estrogens, progestins, PDE5 inhibitors, apomorphine, bisphosphonate, growth factor inhibitors (such as those that inhibit VEGF, IGF and the like), or one or more additional selective androgen receptor modulators (SARMs).

[000301] Additional therapeutic agents that may be administered in combination with a selective androgen receptor modulator compound of Formulae I-XIV as described herein include, but are not limited to: abemaciclib, Abitrexate ® (methotrexate), Abraxane® (paclitaxel albumin-stabilized nanoparticle formulation), ado-trastuzumab emtansine, adriamycin PFS (doxorubicin hydrochloride), adriamycin RDF (doxorubicin hydrochloride), Adrucil® (fluorouracil), Afinitor® (everolimus), alpelisib, anastrozole, Arimidex® (anastrozole), Aromasin® (exemestane), velumab, atezolizumb, bicalutamide, buparlisib, Caelyx® (pegylated liposomal doxorubicin), capecitabine, carboplatin, cisplatin, Clafen® (cyclophosphamide), cyclophosphamide, Cytoxan® (cyclophosphamide), docetaxel, doxorubicin hydrochloride, durvalumab, Efudex® (fluorouracil), Ellence® (epirubicin hydrochloride), entinostat, enzalutamide, epirubicin hydrochloride, eribulin, ethynyl estradiol, everolimus, Evista® (raloxifene), exemestane, Fareston® (toremifene), Faslodex® (fulvestrant), Femara® (letrozole), Fluoroplex® (5-fluorouracil), fluorouracil, fluoxymesterone, Folex® (methotrexate), Folex PFS® (methotrexate), fulvestrant, gemcitabine hydrochloride, Gemzar® (gemcitabine hydrochloride), Halaven® (eribulin mesylate), Herceptin® (trastuzumab), ixabepilone, Ixempra® (ixabepilone), lapatinib ditosylate, letrozole, megestrol acetate, methotrexate, methotrexate FPF (methotrexate), Mexate® (methotrexate), Mexate-AQ® (methotrexate), Neosar® (cyclophosphamide), NeuVax® (nelipepimut-S), Nolvadex® (tamoxifen citrate), paclitaxel, paclitaxel albumin- stabilized nanoparticle formulation, palbociclib, pembrolizumab, Perjeta® (pertuzumab), pertuzumab, Piqray® (alpelisib), raloxifene, ribociclib, tamoxifen citrate, taselisib, Taxol® (paclitaxel), Taxotere® (docetaxel), trastuzumab, tremelimumab, toremifene, Tykerb® (lapatinib ditosylate), vinorelbine, and Xeloda® (capecitabine).

[000302] Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a selective estrogen receptor modulator. Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a selective estrogen receptor degrader (fulvestrant). Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a CDK4/6 inhibitor (palbociclib, ribociclib, abemaciclib, trilaciclib, lerociclib). Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a PIK3A inhibitor (alpelisib, buparlisib, tapelisib). Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a HER2 inhibitor (lapatinib, trastuzumab, neratinib). Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a VEGF-A inhibitor (bevacizumab). Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with a chemotherapeutic agent. In one embodiment, the chemotherapeutic agent is a taxane. In another embodiment, the chemotherapeutic agent is an anthracycline. In one embodiment, the chemotherapeutic agent is an epothilone (ixabepilone). Thus, in one embodiment, the methods of the present invention comprise administering the selective androgen receptor modulator, in combination with an LHRH analog. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator, in combination with a reversible antiandrogen. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator, in combination with an antiestrogen. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator, in combination with an anticancer drug. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator, in combination with a 5-alpha reductase inhibitor. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with an aromatase inhibitor. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a progestin. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with an agent acting through other nuclear hormone receptors. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a selective estrogen receptor modulator (SERM). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a progestin or anti-progestin. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with an estrogen. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a PDE5 inhibitor. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with apomorphine. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a bisphosphonate (pamidronate, zoledronic acid). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a denosumab (Xgeva®). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with a growth factor inhibitor. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with one or more additional selective androgen receptor modulators (SARMs).

[000303] In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Abitrexate® (methotrexate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Abraxane® (paclitaxel albumin- stabilized nanoparticle formulation). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with ado-trastuzumab emtansine. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Adriamycin PFS® (doxorubicin hydrochloride). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Adriamycin RDF ® (doxorubicin hydrochloride). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Adrucil® (fluorouracil). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Afinitor® (everolimus). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with anastrozole. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Arimidex® (anastrozole). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Aromasin® (exemestane). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with capecitabine. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Clafen® (cyclophosphamide). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with cyclophosphamide. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Cytoxan® (cyclophosphamide). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with docetaxel. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with doxorubicin hydrochloride. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Efudex® (fluorouracil). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Ellence® (epirubicin hydrochloride). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with epirubicin hydrochloride. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with everolimus. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with exemestane. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Fareston® (toremifene). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Evista® (raloxifene). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Faslodex® (fulvestrant). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Femara® (letrozole).

[000304] In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Fluoroplex® (5-fluorouracil). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with fluorouracil. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Folex® (methotrexate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Folex PFS® (methotrexate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with fulvestrant. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with gemcitabine hydrochloride. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Gemzar® (gemcitabine hydrochloride). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Herceptin® (trastuzumab). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Ibrance (palbociclib). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Kisquali (ribociclib). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Verenzio (abemaciclib). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with trilaciclib. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with lerociclib. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with ixabepilone. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Ixempra® (ixabepilone). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with lapatinib ditosylate. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with letrozole. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with methotrexate. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with methotrexate LPF (methotrexate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Mexate® (methotrexate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Mexate- AQ® (methotrexate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Neosar® (cyclophosphamide). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator ofFormulae I-XIV as described herein, in combination with Nolvadex® (tamoxifen citrate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with paclitaxel. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with paclitaxel albumin- stabilized nanoparticle formulation. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Perjeta® (pertuzumab). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with pertuzumab. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with tamoxifen citrate. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Taxol® (paclitaxel). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Taxotere® (docetaxel). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator ofFormulae I-XIV as described herein, in combination with trastuzumab. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with oremifene. In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Tykerb® (lapatinib ditosylate). In another embodiment, the methods of the present invention comprise administering a selective androgen receptor modulator of Formulae I-XIV as described herein, in combination with Xeloda® (capecitabine).

[000305] In one embodiment, the methods of the present invention comprise administering a pharmaceutical composition (or pharmaceutical preparation, used herein interchangeably) comprising the selective androgen receptor modulator of Formulae I-XIV as described herein and/or its analog, derivative, isomer, metabolite, pharmaceutical product, hydrate, N-oxide, polymorph, crystal, prodrug or any combination thereof; and a suitable carrier or diluent.

Pharmaceutical Compositions

[000306] As used herein, "pharmaceutical composition" means therapeutically effective amounts of the selective androgen receptor modulator together with suitable diluents, preservatives, solubilizers, emulsifiers, adjuvant and/or carriers. A "therapeutically effective amount" as used herein refers to that amount which provides a therapeutic effect for a given condition and administration regimen. Such compositions are liquids or lyophilized or otherwise dried formulations and include diluents of various buffer content (e.g., Tris-HCl, acetate, phosphate), pH and ionic strength, additives such as albumin or gelatin to prevent absorption to surfaces, detergents (e.g., Tween 20®, Tween 80®, Pluronic F68®, bile acid salts), solubilizing agents (e.g., glycerol, polyethylene glycerol), anti-oxidants (e.g., ascorbic acid, sodium metabisulfite), preservatives (e.g., Thimerosal ®, benzyl alcohol, parabens), bulking substances or tonicity modifiers (e.g., lactose, mannitol), covalent attachment of polymers such as polyethylene glycol to the protein, complexation with metal ions, or incorporation of the material into or onto particulate preparations of polymeric compounds such as polylactic acid, polglycolic acid, hydrogels, etc, or onto liposomes, microemulsions, micelles, unilamellar or multilamellar vesicles, erythrocyte ghosts, or spheroplasts). Such compositions will influence the physical state, solubility, stability, rate of in vivo release, and rate of in vivo clearance. Controlled or sustained release compositions include formulation in lipophilic depots (e.g., fatty acids, waxes, oils). [000307] In one embodiment, the pharmaceutical compositions comprising the SARM compounds of Formulae I-XIV as described herein make use in the methods of this invention of a dosage of between 1 and 50 mg of a SARM compound of Formulae I-XIV as described herein. In another embodiment, the dosage is 1 mg, 3 mg, 9 mg, 10 mg, 18 mg or 30 mg of the SARM compound of Formulae I-XIV as described herein. In another embodiment, the pharmaceutical compositions comprising the SARM compounds as described herein make use in the methods of this invention of a dosage of 1 mg of a SARM compound of Formulae I-XIV as described herein. In another embodiment, the pharmaceutical compositions comprising the SARM compounds of Formulae I-XIV as described herein make use in the methods of this invention of a dosage of 3 mg of a SARM compound of Formulae I-XIV as described herein. In another embodiment, the pharmaceutical compositions comprising the SARM compounds of Formulae I-XIV as described herein make use in the methods of this invention of a dosage of 9 mg of a SARM compound of Formulae I-XIV as described herein. In another embodiment, the pharmaceutical compositions comprising the SARM compounds of Formulae I-XIV as described herein make use in the methods of this invention of a dosage of 10 mg of a SARM compound of Formulae I-XIV as described herein. In another embodiment, the pharmaceutical compositions comprising the SARM compounds as described herein make use in the methods of this invention of a dosage of 18 mg of a SARM compound of Formulae I-XIV as described herein. In another embodiment, the pharmaceutical compositions comprising the SARM compounds of Formulae I-XIV as described herein make use in the methods of this invention of a dosage of 30 mg of a SARM compound of Formulae I-XIV as described herein.

[000308] Also comprehended by the invention are particulate compositions coated with polymers (e.g., poloxamers or poloxamines). Other embodiments of the compositions of the invention incorporate particulate forms protective coatings, protease inhibitors or permeation enhancers for various routes of administration, including parenteral, pulmonary, nasal and oral. In one embodiment the pharmaceutical composition is administered parenterally, paracancerally, transmucosally, transdermally, intramuscularly, intravenously, intradermally, subcutaneously, intraperitoneally, intraventricularly, intravaginally, intracranially and intratumorally.

[000309] Further, as used herein "pharmaceutically acceptable carriers" are well known to those skilled in the art and include, but are not limited to, 0.01-0.1 M and preferably 0.05 M phosphate buffer or about 0.8% saline. Additionally, such pharmaceutically acceptable carriers may be aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non- aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media.

[000310] Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's and fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers such as those based on Ringer's dextrose, and the like. Preservatives and other additives may also be present, such as, for example, antimicrobials, antioxidants, collating agents, inert gases and the like.

[000311] Controlled or sustained release compositions include formulation in lipophilic depots (e.g., fatty acids, waxes, oils). Also comprehended by the invention are particulate compositions coated with polymers (e.g., poloxamers or poloxamines) and the compound coupled to antibodies directed against tissue- specific receptors, ligands or antigens or coupled to ligands of tissue-specific receptors.

[000312] Other embodiments of the compositions of the invention incorporate particulate forms, protective coatings, protease inhibitors or permeation enhancers for various routes of administration, including parenteral, pulmonary, nasal and oral.

[000313] Compounds modified by the covalent attachment of water-soluble polymers such as polyethylene glycol, copolymers of polyethylene glycol and polypropylene glycol, carboxymethyl cellulose, dextran, polyvinyl alcohol, polyvinylpyrrolidone or polyproline are known to exhibit substantially longer half-lives in blood following intravenous injection than do the corresponding unmodified compounds (Abuchowski et al, 1981; Newmark et al, 1982; and Katre et al, 1987). Such modifications may also increase the compound's solubility in aqueous solution, eliminate aggregation, enhance the physical and chemical stability of the compound, and greatly reduce the immunogenicity and reactivity of the compound. As a result, the desired in vivo biological activity may be achieved by the administration of such polymer- compound abducts less frequently or in lower doses than with the unmodified compound.

[000314] In yet another embodiment, the pharmaceutical composition can be delivered in a controlled release system. For example, the agent may be administered using intravenous infusion, an implantable osmotic pump, a transdermal patch, liposomes, or other modes of administration. In one embodiment, a pump may be used (see Langer, supra ; Sefton, CRC Crit. Ref. Biomed. Eng. 14:201 (1987); Buchwald et ai, Surgery 88:507 (1980); Saudek et ai, N. Engl. J. Med. 321:574 (1989). In another embodiment, polymeric materials can be used. In yet another embodiment, a controlled release system can be placed in proximity to the therapeutic target, i.e., the brain, thus requiring only a fraction of the systemic dose (see, e.g., Goodson, in Medical Applications of Controlled Release, supra, vol.2, pp. 115-138 (1984). Other controlled release systems are discussed in the review by Langer (Science 249:1527-1533 (1990).

[000315] The pharmaceutical preparation can comprise the selective androgen receptor modulator alone, or can further include a pharmaceutically acceptable carrier, and can be in solid or liquid form such as tablets, powders, capsules, pellets, solutions, suspensions, elixirs, emulsions, gels, creams, or suppositories, including rectal and urethral suppositories. Pharmaceutically acceptable carriers include gums, starches, sugars, cellulosic materials, and mixtures thereof. The pharmaceutical preparation containing the selective androgen receptor modulator can be administered to a subject by, for example, subcutaneous implantation of a pellet; in a further embodiment, the pellet provides for controlled release of selective androgen receptor modulator over a period of time. The preparation can also be administered by intravenous, intraarterial, or intramuscular injection of a liquid preparation, oral administration of a liquid or solid preparation, or by topical application. Administration can also be accomplished by use of a rectal suppository or a urethral suppository.

[000316] The pharmaceutical preparations of the invention can be prepared by known dissolving, mixing, granulating, or tablet-forming processes. For oral administration, the selective androgen receptor modulators or their physiologically tolerated derivatives such as salts, esters, Mo x ides, and the like are mixed with additives customary for this purpose, such as vehicles, stabilizers, or inert diluents, and converted by customary methods into suitable forms for administration, such as tablets, coated tablets, hard or soft gelatin capsules, aqueous, alcoholic or oily solutions. Examples of suitable inert vehicles are conventional tablet bases such as lactose, sucrose, or cornstarch in combination with binders such as acacia, cornstarch, gelatin, with disintegrating agents such as cornstarch, potato starch, alginic acid, or with a lubricant such as stearic acid or magnesium stearate. [000317] Examples of suitable oily vehicles or solvents are vegetable or animal oils such as sunflower oil or fish-liver oil. Preparations can be effected both as dry and as wet granules. For parenteral administration (subcutaneous, intravenous, intraarterial, or intramuscular injection), the selective androgen receptor modulators or their physiologically tolerated derivatives such as salts, esters, N-oxides, and the like are converted into a solution, suspension, or emulsion, if desired with the substances customary and suitable for this purpose, for example, solubilizers or other auxiliaries. Examples are sterile liquids such as water and oils, with or without the addition of a surfactant and other pharmaceutically acceptable adjuvants. Illustrative oils are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, or mineral oil. In general, water, saline, aqueous dextrose and related sugar solutions, and glycols such as propylene glycols or polyethylene glycols are preferred liquid carriers, particularly for injectable solutions.

[000318] The preparation of pharmaceutical compositions which contain an active component is well understood in the art. Such compositions can be prepared as aerosols of the active component delivered to the nasopharynx or as injectables, either as liquid solutions or suspensions; however, solid forms suitable for solution in, or suspension in, liquid prior to injection can also be prepared. The preparation can also be emulsified. The active therapeutic ingredient is often mixed with excipients which are pharmaceutically acceptable and compatible with the active ingredient. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like or any combination thereof.

[000319] In addition, the composition can contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents which enhance the effectiveness of the active ingredient.

[000320] An active component can be formulated into the composition as neutralized pharmaceutically acceptable salt forms. Pharmaceutically acceptable salts include the acid addition salts (formed with the free amino groups of the polypeptide or antibody molecule), which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed from the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like. [000321] For topical administration to body surfaces using, for example, creams, gels, drops, and the like, the selective androgen receptor modulators or their physiologically tolerated derivatives such as salts, esters, N-oxides, and the like are prepared and applied as solutions, suspensions, or emulsions in a physiologically acceptable diluent with or without a pharmaceutical carrier.

[000322] In another embodiment, the active compound can be delivered in a vesicle, in particular a liposome (see Langer, Science 249:1527-1533 (1990); Treat et ai, in Liposomes in the Therapy of Infectious Disease and Cancer, Lopez- Berestein and Fidler (eds.), Liss, New York, pp. 353-365 (1989); Lopez-Berestein, ibid., pp. 317-327; see generally ibid).

[000323] For use in medicine, the salts of the selective androgen receptor modulator will be pharmaceutically acceptable salts. Other salts may, however, be useful in the preparation of the compounds of Formulae I-XIV as described herein or of their pharmaceutically acceptable salts. Suitable pharmaceutically acceptable salts of the SARM compounds as described herein include acid addition salts which may, for example, be formed by mixing a solution of the SARM compound with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulphuric acid, methanesulphonic acid, fumaric acid, maleic acid, succinic acid, acetic acid, benzoic acid, oxalic acid, citric acid, tartaric acid, carbonic acid or phosphoric acid.

[000324] In one embodiment, the term “about”, refers to a deviance of between 0.0001-5% from the indicated number or range of numbers. In one embodiment, the term “about”, refers to a deviance of between 1-10% from the indicated number or range of numbers. In one embodiment, the term “about”, refers to a deviance of up to 25% from the indicated number or range of numbers.

[000325] In some embodiments, the term “comprise” or grammatical forms thereof, refers to the inclusion of the indicated active agent, such as the SARM compound of Formulae I-XIV as described herein, as well as inclusion of other active agents, and pharmaceutically acceptable carriers, excipients, emollients, stabilizers, etc., as are known in the pharmaceutical industry. In some embodiments, the term “consisting essentially of’ refers to a composition, whose only active ingredient is the indicated active ingredient, however, other compounds may be included which are for stabilizing, preserving, etc. the formulation, but are not involved directly in the therapeutic effect of the indicated active ingredient. In some embodiments, the term “consisting essentially of’ may refer to components, which exert a therapeutic effect via a mechanism distinct from that of the indicated active ingredient. In some embodiments, the term “consisting essentially of’ may refer to components, which exert a therapeutic effect and belong to a class of compounds distinct from that of the indicated active ingredient. In some embodiments, the term “consisting essentially of’ may refer to components, which exert a therapeutic effect and belong to a class of compounds distinct from that of the indicated active ingredient, by acting via a different mechanism of action, for example, and representing an embodiment of this invention, polypeptides comprising T cell epitopes present in a composition may be specifically combined with polypeptides comprising B cell epitopes. In some embodiments, the term “consisting essentially of’ may refer to components which facilitate the release of the active ingredient. In some embodiments, the term “consisting” refers to a composition, which contains the active ingredient and a pharmaceutically acceptable carrier or excipient.

[000326] Further, as used herein, the term “comprising” is intended to mean that the system includes the recited elements, but not excluding others which may be optional. By the phrase “consisting essentially of’ it is meant a method that includes the recited elements but exclude other elements that may have an essential significant effect on the performance of the method. “Consisting of’ shall thus mean excluding more than traces of other elements. Embodiments defined by each of these transition terms are within the scope of this invention.

[000327] In one embodiment, the present invention provides combined preparations. In one embodiment, the term "a combined preparation" defines especially a "kit of parts" in the sense that the combination partners as defined above can be dosed independently or by use of different fixed combinations with distinguished amounts of the combination partners i.e., simultaneously, concurrently, separately or sequentially. In some embodiments, the parts of the kit of parts can then, e.g., be administered simultaneously or chronologically staggered, that is at different time points and with equal or different time intervals for any part of the kit of parts. The ratio of the total amounts of the combination partners, in some embodiments, can be administered in the combined preparation. In one embodiment, the combined preparation can be varied, e.g., in order to cope with the needs of a patient subpopulation to be treated or the needs of the single patient which different needs can be due to a particular disease, severity of a disease, age, sex, or body weight as can be readily made by a person skilled in the art.

[000328] In one embodiment, the term “a” or “one” or “an” refers to at least one. In one embodiment the phrase “two or more” may be of any denomination, which will suit a particular purpose. In one embodiment, “about” may comprise a deviance from the indicated term of + 1%, or in some embodiments, - 1%, or in some embodiments, ± 2.5%, or in some embodiments, ± 5%, or in some embodiments, ± 7.5%, or in some embodiments, ± 10%, or in some embodiments, ± 15%, or in some embodiments, ± 20%, or in some embodiments, ± 25%. [000329] The following examples are presented in order to more fully illustrate the preferred embodiments of the invention. They should in no way be construed, however, as limiting the broad scope of the invention.

EXPERIMENTAL DETAILS SECTION

General Experimental Methods Cell Growth Conditions

[000330] HCC 1937, HCC 1954, HCC 38, T47D-Kbluc, MDA-MB-453, and MDA-MB-231 cells were grown in RPMI-1640 medium containing 2 mM L-glutamine supplemented with 10% fetal bovine serum (FBS). Cells were maintained in a 5% C0 ₂ /95% air humidified atmosphere at 37°C. MCF-7 cells were grown in Minimum Essential Medium supplemented with 10% FBS.

[000331] Breast cancer tumors typically express AR 70-90% of the time, however breast cancer cell lines typically do not express AR. This makes development of a preclinical model for the study of androgen effects on breast cancer very difficult. Consequently, the AR has been introduced by adenoviral infection (stably incorporated into the genome) into some breast cancer cell lines used in the studies below.

Sulforhodamine B (SRB) assay

[000332] The SRB assay was used to determine cell number during cytotoxocity experiments. The following protocol was used:

1. Cells were detached with 0.25% trypsin. 2. Experimental cultures were cultured in 96- well microtiter plates (200 pL growth medium per well; 1,000-200,000 cells per well).

3. Cultures were fixed with 50 pL 50% TCA (4°C). (see cell fixation protocol for details).

4. Fixed cells were stained with 50 pL 0.4% (wt/vol) SRB in 1% acetic acid for 10 minutes.

5. SRB was removed and the cultures were quickly* rinsed 5 times with 1% acetic acid to remove unbound dye.**

6. Cultures were air-dried overnight until there was no visible moisture.

7. The cellular protein-bound SRB was dissolved with 200 m L unbuffered Tris base (10 mM, pH 10.5) for 30 minutes on a rocking platform shaker.

8. Absorbance was read at 540 nm.

* quickly performing rinsing process was to prevent desorption of protein-bound SRB ** completely removed residual wash solution by sharply flicking plates over sink.

Fixation of cells attached to the plastic substratum

[000333] The following protocol was used for fixing cells: a. 50 pL of 50% TCA (4°C) was gently layered on the top of growth medium in each well to make a final TCA concentration of 10%. b. Cultures were incubated at 4°C for 1 hour. c. Cultures were washed 5 times with tap water to remove TCA, growth medium, low- molecular-weight metabolites, and serum protein. d. Plates were air-dried until there was no visible moisture.

EXAMPLE 1

EFFECT OF FORMULA IX ON GROWTH IN DIFFERENT BREAST CANCERS CELL LINES EXPRESSING ANDROGEN RECEPTOR

Materials and Methods:

[000334] MDA-MB-231 and HCC-38 triple negative breast cancer cells were used to analyze growth effects of various compounds.

[000335] MDA-MB-231 and HCC-38 triple negative breast cancer cells were infected with 200 pL or 500 pL adenovirus containing LacZ (negative control) or AR, and were treated with various AR ligands (agonists: DHT and Formula IX, and antagonist: bicalutamide) or a non- AR binder that is structurally similar to Formula IX, /^-enantiomer of Formula IX. Cells were treated in charcoal stripped FBS (Figures 1C, IE, 1G and II; 2C, 2E and 2G or full serum (Figures ID, IF, 1H and 1J; 2D, 2F and 2H for 3 days, fixed and stained with sulforhodamine blue (SRB) to measure cell viability. IC50 values were calculated. Results:

[000336] Expression of AR in cells infected with AR or LacZ was evaluated using Western blotting (Figure 1A and Figure 2A).

[000337] Only the AR agonists, DHT and Formula IX, inhibited MDA-MB-231 and HCC- 38 triple negative breast cancer cell growth (Figures 1C, ID, IE, IF and Figures 2C, 2D, 2E and 2F). This inhibition was observed only in the presence of AR (compare w/lacZ and w/AR). IC50 values in AR-positive cells for DHT and Formula IX are presented in Figure IB and Figure 2B.

EXAMPLE 2 REVERSAL OF EFFECT OF FORMULA IX ON GROWTH

Materials and Methods:

[000338] To determine if the growth inhibition observed with DHT and Formula IX in AR- positive cells is AR dependent, MDA-MB-231 cells were infected with adenovirus containing FacZ (negative control) or AR and were treated with AR agonists, DHT or Formula IX, in the presence or absence of the AR antagonist, bicalutamide. Cells were treated in charcoal stripped FBS (Figures 3A and 3C or full serum (Figures 3B and 3D for 3 days, fixed and stained with sulforhodamine blue (SRB) to measure cell viability. IC ₅₀ values were calculated.

Results:

[000339] Both DHT and Formula IX required AR to inhibit MDA-MB-231 cell growth, as demonstrated by the weakened growth inhibitory effects in the presence of bicalutamide (Figures 3A-3D). IC ₅₀ values for DHT and Formula IX in AR-positive cells pretreated with or without bicalutamide are presented in Figure 3E.

EXAMPLE 3

EFFECT OF AR LIGANDS ON BREAST CANCER CELL GROWTH Materials and Methods:

[000340] To determine if all AR ligands inhibit the growth of triple negative breast cancer cells, MDA-MB-231 cells were infected with adenovirus containing FacZ or AR and were treated with various AR ligands (agonists: DHT, Formula VIII, Formula IX, Formula X, Formula XIII, Formula XIV ; antagonist: bicalutamide) and a non- AR-binder: /^-enantiomer of Formula IX. Cells were treated in charcoal stripped FBS (Figures 4A, 4C, 4E, 4G, 41, 4K, 4M and 40) or full serum (Figures 4B, 4D, 4F, 4H, 4J, 4L, 4N and 4P) for 3 days, fixed and stained with sulforhodamine blue (SRB) to measure cell viability. Anti-proliferative IC50 values were calculated in breast cancer cells and compared to transactivation values, i.e., EC50 (agonists) and IC50 (antagonists) values, generated in HEK-293 cells. The growth regulatory properties in breast cancer cells of these molecules in breast cancer cells are comparable to the transactivation values obtained in HEK-293 cells.

Results:

[000341] Only AR agonists inhibited the growth of MDA-MB-231 cells (Figures 4A, 4B, 4E- 4H, and 4K-4P) and the growth inhibitory potential of these ligands rank order with their agonistic activity observed in HEK-293 cells (Figure 4Q).

[000342] Example 4 demonstrates as well that AR agonists inhibited the proliferation of MDA-MB-231 cells stably transfected with AR.

EXAMPLE 4 AR TRANSACTIVATION ASSAYS IN BREAST CANCER CELLS

Materials and Methods:

[000343] To ensure that the ligands that elicited growth inhibitory properties are agonists in MDA-MB-231 cells, AR transactivation assays were performed in MDA-MB-231 cells. Though AR transactivation assay was performed in HEK-293 cells, the ability of ligands to function as agonists or antagonists depends on cellular microenvironment. Hence, MDA-MB- 231 cells were transfected using lipofectamine with AR, GRE-LUC and CMV-LUC as normalization control. The cells were treated 24 h after transfection and luciferase assay performed 48 h after transfection.

Results: [000344] Figure 5 shows that all AR ligands that elicited anti-proliferative activity are agonists in MDA-MB-231 cells transfected with AR and their agonist and growth inhibitory properties compare well. In other words, growth inhibitory ligands are AR agonists in MDA- MB-231 cells transfected with AR. EXAMPLE 5

ANALYSIS OF GROWTH INHIBITORY EFFECTS IN BREAST CANCER CELLS EXPRESSING ESTROGEN RECEPTOR

Materials and Methods:

[000345] To ensure that growth inhibitory effects in MDA-MB-231 cells are selective to AR, and to determine if the ligand dependent growth inhibitory effects are exclusive to AR and also to ensure that the effects are not artifacts of adenoviral infection, MDA-MB-231 triple negative breast cancer cells were infected with ER-a or ER-b adenovirus constructs and were treated with ER agonist: 17 b-estradi ol (E2) or ER antagonist: ICI 182,780 (ICI) in charcoal stripped serum (Figure 6C) or full serum (Figures 6D and 6E) for 3 days. Cells were fixed and stained with sulforhodamine blue (SRB) to measure cell viability. Expression of ER in infected cells was evaluated using Western blotting.

Results:

[000346] Figures 6A-6B show the presence or absence of ERa or Eϋb in MDA-MB-231 cells following transfection. These results show that the anti-proliferative effects observed with androgens is unique to ligand activated AR and not an artifact of adenovirus. Figures 6C-6E show that over-expression of ER-a or ER-b in MDA-MB-231 cells failed to promote growth inhibition either in the presence of ER agonists or antagonists. Thus, the observed growth inhibitory effects in MDA-MB-231 cells are selective to the presence of the AR and AR agonists.

EXAMPLE 6

EFFECT OF AR AGONIST ON MORPHOLOGY OF BREAST CANCER CELLS

Materials and Methods:

[000347] MDA-MB-231 cells were stably transfected with AR using lentivirus. Following transfection, cells were treated for 3 days with the indicated concentrations of DHT or bicalutamide. Live cells were visualized using a light-microscope and photographed. The cells were imaged at the same magnification and under the same microscopic conditions.

Results:

[000348] Figure 7 shows that DHT altered the morphology of MDA-MB-231 cells into more anchorage dependent and differentiated cells, indicating that AR agonist-bound AR expressing breast cancer cells will have less invasive and migratory properties (e.g., less likely to metastasize).

[000349] DHT and SARMs alter the morphology of AR-positive MDA-MB-231 cells. MDA- MB-231 cells were stably transfected with AR using lentivirus and were treated with vehicle or AR agonists at the indicated concentrations. At the end of 3 days of incubation, the cells were imaged under a microscope (40X).

[000350] DHT and SARMs, but not the AR antagonist, bicalutamide (data not shown), or the inactive isomer of Formula IX, altered the morphology of the cells into a more anchorage- dependent phenotype (Figure 12).

EXAMPLE 7

CROSS-REACTIVITY OF FORMULA VIII WITH OTHER NUCLEAR HORMONE

RECEPTORS

[000351] In order to determine whether SARM compounds of Formulae I-XIV as described hereinaffected other nuclear hormone receptor signaling, the ability of a compound represented by Formula VIII to stimulate (agonist) or inhibit (antagonist) ERa-, Eϋb-, GR-, PR-, or MR- mediated transcriptional activation, was analyzed.

Materials and Methods:

Transient Transfection

[000352] Rat GR, MR, PR, ER-oc and ER-b were individually cloned into a pCR3.1 vector backbone. Sequencing was performed to verify the absence of any mutations. HEK-293 cells were plated at 90,000 cells per well of a 24 well plate in Dulbecco’s Minimal Essential Media supplemented with 5% charcoal-stripped FBS. The cells were transfected using Lipofectamine (Invitrogen, Carlsbad, CA) with 0.25 qg GRE-LUC for GR, MR and PR and ERE-LUC for ER- oc and ER-b, 0.5 ng CMV-LUC (renilla luciferase) and 12.5-25 ng of the respective expression vector for each receptor. The cells were treated 24 h after transfection with Formula VIII in the absence (agonist mode) and presence (antagonist mode) of known agonists (17β-estradiol for ER; dexamethasone for GR; aldosterone for MR; progesterone for PR) as controls. Luciferase assays were performed 48 h after transfection. Transcriptional activation values are represented as firefly luciferase normalized to renilla luciferase.

Results: [000353] The agonist effects of Formula VIII on ER-b, ER-oc, GR, PR and MR were tested and compared to the activities of the known ligands, as well (Figure 8). A compound of Formula VIII failed to activate ER-b or ER-oc even at the highest tested concentration (1 mM) whereas 1 nM 17β-estradiol induced ERa- and ERb-mediated transactivation by 3- and 5-fold, respectively. A compound of Formula VIII failed to activate GR- or MR-mediated transactivation. A compound of Formula VIII at all the tested concentrations did not induce GR- or MR-mediated transactivation, whereas the known ligands (dexamethasone and aldosterone) induced the activities of GR or MR by 70- and 60-fold, respectively, at a concentration of 1 nM. However, a compound of Formula VIII increased the transactivation of PR at 1 mM and 10 mM by 3 and 8 fold, respectively. Progesterone activated PR by 23 folds at a 1 nM concentration, indicating that a compound of Formula VIII is greater than 10,000-fold weaker than the endogenous agonist for PR.

[000354] The ability of a compound of Formula VIII to inhibit the effects of a known agonist for each of the above mentioned receptors was tested as well.

[000355] Co-incubation of HEK 293 cells with the indicated concentrations of Formula VIII failed to alter the 17b-estradiol-induced ER-b or ER-oc activity, dexamethasone-induced GR- mediated transactivation or aldosterone-induced MR-mediated transactivation.

[000356] A dose response curve for a compound of Formula VIII in antagonist mode demonstrated potent partial inhibition of PR activity (Figure 9). In comparison to Formula IX, Formula VIII was 10-times more potent, and 100-times more potent than /^-enantiomer of Formula IX. In comparison to RU486, Formula VIII was about 1,000 fold weaker as a PR antagonist, than RU486.

[000357] Compounds of Formulae VIII and IX are specific for the AR and do not stimulate or inhibit receptor-mediated transactivation of ERa, ERb, GR, or MR. Unexpectedly, Formula VIII exhibited moderate potency partial agonist activity for PR, and potent PR partial antagonism (see Figure 9). Combined AR-agonism and PR-antagonism will be beneficial in certain breast cancers (e.g., PR-positive breast cancers).

EXAMPLE 8

FORMULA VIII AND FORMULA IX INHIBIT TRIPLE NEGATIVE BREAST CANCER CELL TUMOR GROWTH IN MICE Materials and Methods:

[000358] MDA-MB-231-AR triple negative breast cancer cells (2 million cells/mouse; MDA- MB-231 cells stably transfected with AR using lentivirus) were mixed with matrigel (1:1) and injected subcutaneously into the flanks of intact female nude mice (n=5/group). When the tumors reached 150-200 mm ³ , the animals were separated into two groups, one receiving vehicle and the other receiving 30 mg/kg Formula VIII orally. Tumor volume was measured thrice weekly and % tumor growth inhibition (TGI) was calculated. At the end of 35 days of treatment, the animals were sacrificed, tumors excised, weighed, and collected for various analyses. Blood was collected and serum separated for drug concentration measurement.

Results:

[000359] Formula VIII significantly reduced the tumor growth with TGI of -75% (Figure 10B). Tumor weights were also reduced by more than 50% by Formula VIII treatment (Figure 11, right panel) as were tumor size (Figure 11, left panel (mm ³ ) and middle panel (% change)). Formula VIII elicited these results without any associated toxicity or changes in body weight (Figure 10A). Uterus weight also increased in response to Formula VIII treatment (not shown), indicative of in vivo androgenic response.

[000360] The results presented in Figure 24 shows the increase of body weight by the SARMs at all doses of Formula VIII and Formula IX, indicative of healthy growth and a lack of toxicity. By comparison, the vehicle treated animal did not grow as robustly.

[000361] In summary, the Formula VIII SARM is extremely effective in regressing the growth of AR expressing triple negative breast cancer xenografts in mice, and is likely to be effective in a wide variety of AR-positive breast cancers in humans, as described supra and infra.

EXAMPLE 9

EFFECT OF FORMULA IX IN WOMEN WITH METASTATIC OR ER AND/OR AR- POSITIVE REFRACTORY BREAST CANCER

[000362] This clinical trial assessed the safety and efficacy of 9 mg of the compound represented by the structure of Formula IX (Formula IX), in 22 post-menopausal women who have estrogen receptor (ER) positive metastatic breast cancer, and who have responded previously to adjuvant and/or salvage endocrine therapy. The goal of this study was to determine the importance of the AR status as a therapeutic target in women with ER-positive metastatic breast cancer (MBC) that had previously responded to hormone therapy. The treatment was continued until disease progression (PD).

[000363] Primary endpoint was clinical benefit response (CBR) by 6 months (m) defined as patients having a complete response (CR), partial response (PR), or stable disease (SD). CBR will be correlated with AR status of metastatic tumor biopsy.

[000364] Seram prostate specific antigen (PSA) was evaluated as a biomarker of AR activity.

[000365] Results: Formula IX was well-tolerated, with no drug related serious adverse events and none exceeding Grade 3. Conclusions: Formula IX demonstrated promise as a novel targeted therapy for AR-positive MBC. The primary endpoint has been achieved, with 6/17 AR+ patients meeting statistical threshold for success, as outlined in the Tables 1-5 herein below. Serum PSA appeared to be a surrogate marker for AR activity and disease response.

Materials and Methods:

Subject Population [000366] Female subjects with ER-positive metastatic breast cancer who have previously been treated with up to 3 prior hormonal therapies for the treatment of breast cancer. Subjects must have been treated with and responded to previous adjuvant therapy for > 3 years or hormonal therapy for metastatic disease for > 6 months prior to progression. Details of subject selection criteria are presented below: [000367] To be eligible for participation in this study, subjects must meet all of the following criteria, including give voluntary, signed informed consent in accordance with institutional policies; be a woman that has been diagnosed with ER-positive metastatic breast cancer; and be clinically confirmed as postmenopausal. Subjects must have undergone the onset of spontaneous, medical or surgical menopause prior to the start of this study. (Spontaneous menopause is defined as the natural cessation of ovarian function as indicated by being amenorrheic for at least 12 months. If the subject has been amenorrheic for > 6 months but < 12 months they must have a serum FSH concentration of > 50 mlU/mL and an 17 b-estradiol concentration of < 25 pg/mL; medical menopause is defined as treatment with a luteinizing hormone receptor hormone agonist; and surgical menopause is defined as bilateral oophorectomy).

[000368] Additional requirement that subjects must meet include that they have been treated and responded to previous adjuvant hormonal therapy for > 3 years or previous hormonal therapy for metastatic disease for > 6 months prior to disease progression; that they have not had radiation therapy for breast cancer within 2 weeks of randomization in this study and are not planned to have radiation therapy during participation in this study. Subjects must be willing to provide tissue sample from a biopsy of a metastatic tumor lesion(s) for determination of AR and ER status. Tissue samples from a biopsy of a primary tumor lesion will also be provided if available. Further subjects must have ECOG score < 2 and be age > 18 years.

[000369] Subjects with any of the following exclusion criteria will NOT be eligible for enrollment in this study: have triple negative breast cancer; have, in the judgment of the Investigator, a clinically significant concurrent illness or psychological, familial, sociological, geographical or other concomitant condition that would not permit adequate follow-up and compliance with the study protocol; have uncontrolled hypertension, congestive heart failure or angina; have Stage 4 chronic obstructive pulmonary disease (COPD); have positive screen for hepatitis B consisting of HBsAg (Hepatitis B Surface Antigen), unless subject was diagnosed > 10 years prior to enrollment and no evidence of active liver disease; have ALT/SGOT or AST/SGPT above 1.5 times the upper limit of normal (ULN); have positive screen for hepatitis A antibody IgM or HIV ; have received chemotherapy for metastatic breast cancer within the 3 months prior to enrollment in the study or be expected to receive chemotherapy for metastatic breast cancer during the study; be currently taking testosterone, methyltestosterone, oxandrolone (Oxandrin®), oxymetholone, danazol, fluoxymesterone (Halotestin®), testosterone-like agents (such as dehydroepiandrosterone (DHEA), androstenedione, and other androgenic compounds, including herbals), or antiandrogens; previous therapy with testosterone and testosterone-like agents is acceptable with a 30-day washout (if previous testosterone therapy was long term depot within the past 6 months, the site should contact the medical monitor for this study to determine appropriate washout period); have untreated or uncontrolled brain metastasis; have been diagnosed with or treated for cancer within the previous two years, other than breast cancer or non-melanoma carcinoma of the skin

[000370] Androgen receptor (AR) status was assessed in all subjects from primary and/or metastatic lesions after enrollment. It was observed that the majority (17/19) of subjects with ER-positive breast cancer also expressed AR) in their primary tumor samples, which correlated well with previous literature which predicted 70-95% would be AR-positive (Niemeier LA, et.al. Androgen receptor in breast cancer: expression in estrogen receptor-positive tumors and in estrogen-negative tumors with apocrine differentiation. Modern Pathology 23:205-212, 2010; Narita D, et al. Immunohistochemical expression of androgen receptor and prostate- specific antigen in breast cancer. Folia Flistochemica Et Cytobiologica 44: 165- 172, 2006). High percentages (72-84%) of metastatic lesions obtained from women with advanced breast cancer have also been found to be AR-positive (Lea OA. et al. Improved measurement of androgen receptors in human breast cancer. Cancer Research 49:7162-7167, 1989).

[000371] As 70% or greater of the women with ER-positive breast cancer were expected to have tumors that are AR-positive, the study was designed to enroll approximately 27 subjects (of 40 originally intended to be enrolled) with AR-positive breast cancer in each dose arm, enabling assessment of the primary endpoint in AR-positive subjects, as well as the secondary and tertiary endpoints in subsets based on AR status (i.e., all subjects, AR-positive subjects, and AR-negative subjects).

[000372] At the time of this writing, patient demographics were: mean age 63.7 years, mean time from diagnosis 11.0 years, 72.7% prior chemotherapy, 89% (17/19) AR-f, 41% delectable baseline PSA and 86.4% previous radiation. [000373] Table 1; The baseline characteristic by response was as follows:

Table 2: Table of Subjects Assessed as Having Clinical Benefit as Best Response

10

Table 3: Table of Subjects Assessed as Having Clinical Benefit at 6 Months

5

10

Table 4: Table of Subjects Assessed as Having Progressive Disease at 6 Months or Prior

Treatment

[000374] Subjects received 9 mg daily dose of Formula IX, with baseline and regular on study assessments of safety and efficacy. [000375] Measurable and non-measurable lesions (primary and/or metastatic) were identified and assessed by a modified Response Evaluation Criteria In Solid Tumors (RECIST 1.1) classification over the course of this study (described in detail below).

Study Duration

[000376] Each subject enrolled into this study received intervention until a progression free survival (PFS) endpoint has been reached (tumor progression or death). Subjects will be followed after treatment has been discontinued for vital status only.

Efficacy Endpoints

[000377] The primary efficacy analysis was the clinical benefit in subjects with AR-positive breast cancer at 6 months as measured by a modified Response Evaluation Criteria in Solid Tumors (RECIST 1.1) classification. Key secondary endpoints of clinical benefit in all subjects and AR-negative subjects, as well as objective response rate, progression free survival, time to progression, duration of response, incidence of SREs, and time to first SRE in subsets based on AR status (i.e., all subjects, AR-positive subjects, and AR-negative subjects) was also assessed. Effects on CA 27-29, PSA, bone turnover markers, QOL, and libido were assessed as tertiary endpoints.

Primary Endpoint

[000378] Clinical benefit in a subject is defined as a complete response [CR], a partial response [PR] or stable disease [SD] as measured by modified RECIST 1.1, which is described in detail below. (Eisenhauer EA et al. New response evaluation criteria in solid tumors: revised RECIST guideline (version 1.1). European Journal of Cancer 45:228-247, 2009).

[000379] For subjects with non-measurable (non-target) disease only at baseline, SD was defined as those with non-CR/non-PD combined response. The primary endpoint of the study was to assess the proportion of subjects with clinical benefit (PCB) at 6 months (CR+PR+SD) in subjects with AR-positive breast cancer.

Secondary Endpoints

[000380] The secondary efficacy endpoints include: · To assess the clinical benefit in all subjects with breast cancer treated with

Formula IX. The clinical benefit is defined as the proportion of subjects with complete response [CR] + partial response [PR] + stable disease [SD] as measured by modified RECIST 1.1 (Eisenhauer EA et al. New response evaluation criteria in solid tumors: revised RECIST guideline (Version 1.1). European Journal of Cancer 45: 228-247, 2009). · For subjects with non-measurable (non-target) disease only at baseline, SD was defined as those with non-CR/non-PD combined response.

• To assess objective response rate (ORR) in subjects with breast cancer treated with Formula IX. Objective response rate is defined as the proportion of subjects with a CR or PR at 6 months as measured by modified RECIST 1.1. For subjects with non-measurable (non- target) disease only at baseline, ORR is defined as the proportion of subjects with a CR at 6 months as measured by modified RECIST 1.1.

• To assess progression free survival (PFS) in subjects with breast cancer treated with Formula IX. PFS is defined as the time elapsed between treatment initiation and tumor progression as measured by modified RECIST 1.1 OR death. · To assess time to progression (TTP) in subjects with breast cancer treated with

Formula IX. Time to tumor progression is defined as the time elapsed between treatment initiation and tumor progression as measured by modified RECIST 1.1.

• To assess duration of response in subjects with breast cancer treated with Formula IX. · To assess incidence of skeletal related events (SREs) in subjects treated with

Formula IX.

• To assess time to first skeletal related event (SRE) in subjects treated with

Formula IX. Tertiary Endpoints

• To assess serum CA 27-29 changes in subjects with breast cancer treated with Formula IX.

• To assess serum PSA changes in subjects with breast cancer treated with Formula IX.

• To assess changes in bone turnover markers (serum osteocalcin, serum collagen type I cross linked C-telopeptide [CTX], serum collagen type I cross linked N-telopeptide [NTX], serum bone specific alkaline phosphatase, and urinary NTX in subjects treated with Formula IX.

• To assess the effect of Formula IX on quality of life (QOL) as measured by FACIT-F questionnaire in subjects treated with Formula IX.

• To assess the effect of Formula IX on libido as measured by female sexual function index (FSFI) questionnaire in subjects treated with Formula IX.

• To explore the relationship of various levels of AR expression as determined by immunohistochemistry with primary, secondary and tertiary objectives.

Results:

[000381] After a median follow-up of 81 days (d) (range 7-304 d), preliminary results of the 22 patients were as follows: 9 SD was observed as best response, median duration 212 d. Current disposition of all patients: 15 PD after a median 80 d (range 15 -304 d), 4 SD, and 3 early discontinuations (d 7, 28, 255). Among patients who reached 6 m, six are AR-positive with SD and increased PSA. 1 has yet to reach 6 m and no CR or PR has been observed. Formula IX was well-tolerated, with no drug related serious adverse events and none exceeding Grade

[000382] No useful trends were seen with the biomarkers of bone turnover: bone specific alkaline phosphatase, C-telopeptides, N-telopeptides, and osteocalcin. Likewise breast cancer biomarker CA 27-29 did not demonstrate any useful trends.

[000383] PSA levels appeared to increase in response to Formula IX treatment as was observed in 20 of the 22 patients measured, but correlation with clinical benefit or disease progression is not yet evident. [000384] The following non serous adverse events were observed:

[000385] A-fib(l); anxiety/emotional changes (5), arthralgia (6), bloating (2), bruising (1), cellulitis (1), chills (1), constipation (2), cough (1), dehydration (1), diarrhea (3), dizziness (2), dysgeusia (1), dyspepsia (1), dyspnea (3), edema (2), fatigue (14), fever (1), flatulence (1), glaucoma (1), headache (4), hot flash night sweats (7), hypertension (2), infection (1), insomnia (2), myalgia (5), nail discoloration (1), nausea (11), pain (22), paresthesia (1), pleural effusion (1), polyuria (1), post menopausal bleeding (3), rash/acne (3), stiffness (1), tendonitis (1), vision changes (3), vomiting (2), weight gain (2), and weight loss (2).

[000386] The liver enzymes (ALT, AST and bilirubin) returned to baseline with no interruption of therapy and no increase in total bilirubin.

[000387] Conclusions: Formula IX demonstrated promise as a novel targeted therapy for AR-positive MBC. The primary endpoint was achieved, with 6/17 AR-positive patients meeting statistical threshold for success. Serum PSA appeared to be a surrogate marker for AR activity and disease response.

[000388] Table 5: AR Status and Patient Disposition

Modified RECIST 1.1

[000389] The modified RECIST 1.1 definitions described below was applied:

Measurable Lesions

[000390] A measurable lesion is defined as one lesion whose longest diameter (LD) can be accurately measured as > 10 mm CT or MRI technique by using a 5 mm contiguous reconstruction algorithm.

[000391] Measurable lesions must be at least 2 times the slice thickness or at least two times the size of the CT scan interval cut.

[000392] Lesions seen on chest x-ray but not confirmed by CT or MRI scan are not acceptable as measurable lesions for this study.

[000393] To be considered pathologically enlarged and measurable, a lymph node must be > 15 mm in short axis when assessed by CT scan (CT scan slice thickness recommended to be no greater than 5 mm). At baseline and in follow-up, only the short axis will be measured and followed. [000394] Measurable disease is defined as the presence of at least one measurable lesion.

[000395] All measurements will be taken and recorded in millimeters using an electronic measurement method.

Non-Measurable Lesions

[000396] Non-measurable lesions are defined as any lesion(s) that are smaller than the criteria for measurable lesions stated above (non-nodal lesions with longest diameter < 10mm or pathological lymph nodes with > 10 mm to < 15 mm in short axis) or truly non measurable lesions (or sites of disease). Lesions considered to be truly non-measurable are bone lesions (lytic lesions or mixed lytic -blastic lesions without identifiable soft tissue components, and blastic lesions), leptomeningeal disease, ascites, pleural/pericardial effusions, lymphangitis cutis/pulmonis, inflammatory breast disease, abdominal masses not confirmed by imaging techniques, and cystic lesions.

Target Lesions [000397] Target lesions must be measurable lesions.

[000398] All target lesions up to a maximum of two lesions per organ and five lesions in total, representative of all involved organs, will be selected/confirmed as target lesions, recorded and measured at baseline. [000399] Target lesions should be selected on the basis of their size (lesions with the longest diameter) and their suitability for accurate repetitive measurements by CT/MRI imaging techniques and be most representative of the subject’s tumor burden.

[000400] Target lesions will be measured in one dimension by the size estimation of their diameter. A sum of the diameters (longest for non-nodal lesions and shortest for nodal lesions) for all target lesions will be calculated and reported for each time point. The baseline sum of diameters will be used as reference to further characterize the objective tumor response of the measurable dimension of the disease.

Non -Target Lesions

[000401] All other lesions (or sites of disease) and any measurable lesions that were not selected as target lesions should be identified as non-target lesions and indicated as present at baseline.

[000402] Measurements of the non-target lesions may be performed, however the continued presence or absence as well as the disappearance or progression status of these lesions will be noted throughout follow-up assessments. New Lesions

[000403] New lesions will be called at follow-up visits regardless of whether they occur in anatomic regions that were routinely subjected to follow-up, or in regions without disease at baseline and for which a follow-up scan is performed for clinical suspicion of new disease. New lymph nodes need to have a minimum size of 10 mm in their shortest axis. New non- nodal lesions need not to be measurable or to have a minimum size. Measurements of new lesions may be performed.

Response Criteria Definitions

[000404] The following response criteria will be applied for target and non- target lesions: Target Lesion Response Criteria

[000405] Complete Response (CR): Disappearance of all target lesions. Target lymph node lesions that become < 10 mm in their shortest diameter will be considered to be normal (non- pathologic) and their actual measurement will be recorded. Thus, it follows that if all target node lesions have become < 10 mm, and all other non-nodal lesions have disappeared (whether target or non-target type), the overall response will be considered to be a CR.

[000406] Partial Response (PR): At least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum of the diameters.

[000407] Stable Disease (SD): Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as reference the smallest sum of diameters (nadir).

[000408] Progressive Disease (PD): At least a 20% increase in the sum of the diameters of target lesions taking as reference the smallest sum of diameters (nadir) recorded since the treatment started. In addition to the relative increase of 20%, the sum of diameters must also demonstrate an absolute increase of at least 5 mm. [000409] Not evaluable (NE): NE can be applied if repeated measurements cannot be assessed for reasons such as inadequate or missing imaging.

Non -Target Lesion Response Criteria

[000410] Complete Response (CR): Disappearance of all non-target lesions. All lymph nodes must be non-pathological in size (< 10 mm short axis). Disappearance of bone lesions identified on bone scintigraphy.

[000411] Non-CR/Non-PD: Persistence of one or more non-target lesions. Stability, decrease, or mild increase in uptake of bone lesions on bone scintigraphy.

[000412] Progressive Disease (PD): Unequivocal progression of existing non-target lesions. A perceived increase in bone disease in a preexisting area will not be considered progression. For bone scintigraphy, at least two new lesions are required to conclude to a definite presence of new lesions unless one or more of these lesions are confirmed by radiography, CT or MRI.

[000413] Not Evaluable (NE): NE can be applied if repeated evaluations cannot be assessed for reasons such as inadequate or missing imaging.

Definitions of Combined Response at Each Time Point [000414] Determination of an overall response for each time point is based on the combination of responses for target, non-target, and the presence or absence of new lesions using the algorithm outlined on tables Cl and C2 below.

Table Cl: Summary of Definitions of Response for Patients with Measurable (Target) Disease at Baseline

Table C2: Summary of Definitions of Response for Patients with Non-Measurable (Non -Target) Disease only at Baseline

EXAMPLE 10

SYNTHESIS OF (S) ENANTIOMER OF FORMULA VIII

[000415] (2R)-l-Methacryloylpyrrolidin-2-carboxylic Acid. D-Proline, 14.93 g, 0.13 mol) was dissolved in 71 mL of 2 N NaOH and cooled in an ice bath; the resulting alkaline solution was diluted with acetone (71 mL). An acetone solution (71 mL) of methacryloyl chloride (13.56 g, 0.13 mol) and 2 N NaOH solution (71 mL) were simultaneously added over 40 min to the aqueous solution of D-proline in an ice bath. The pH of the mixture was kept at 10-11°C during the addition of the methacryloyl chloride. After stirring (3 h, room temperature), the mixture was evaporated in vacuo at a temperature at 35-45°C to remove acetone. The resulting solution was washed with ethyl ether and was acidified to pH 2 with concentrated HC1. The acidic mixture was saturated with NaCl and was extracted with EtOAc (100 mL x 3). The combined extracts were dried over Na ₂ SO ₄ , filtered through Celite®, and evaporated in vacuo to give the crude product as a colorless oil. Recrystallization of the oil from ethyl ether and hexanes afforded 16.2 g (68%) of the desired compound as colorless crystals: mp 102-103°C; the NMR spectrum of this compound demonstrated the existence of two rotamers of the title compound. ¹ H NMR (300 MHz, DMSO-iL) d 5.28 (s) and 5.15 (s) for the first rotamer, 5.15 (s) and 5.03 (s) for the second rotamer (totally 2H for both rotamers, vinyl CH2), 4.48-4.44 for the first rotamer, 4.24-4.20 (m) for the second rotamer (totally 1H for both rotamers, CH at the chiral canter), 3.57-3.38 (m, 2H, CH2), 2.27-2.12 (1H, CH), 1.97- 1.72 (m, 6H, CH ₂ , CH, Me); ¹³ C NMR (75 MHz, DMSO-d ₆ ) d for major rotamer 173.3, 169.1, 140.9, 116.4, 58.3, 48.7, 28.9, 24.7, 19.5: for minor rotamer 174.0, 170.0, 141.6, 115.2, 60.3,

45.9, 31.0, 22.3, 19.7; IR (KBr) 3437 (OH), 1737 (C=0), 1647 (CO, COOH), 1584, 1508,

1459, 1369, 1348, 1178 cm ¹ ; [α ]D ²⁶ +80.8° = 1, MeOH); Anal. Calcd. for C ₉ H13NO3: C 59.00, H 7.15, N 7.65. Found: C 59.13, H 7.19, N 7.61. [000416] (3R,8aR)-3-Bromomethyl-3-methyl-tetrahydro-pyrrolo[2,l-c][l, 4]oxazine-

1,4-dione. A solution of NBS (23.5 g, 0.132 mol) in 100 mL of DMF was added dropwise to a stirred solution of the (methyl- aery loyl) -pyrrolidine (16.1 g, 88 mmol) in 70 mL of DMF under argon at room temperature, and the resulting mixture was stirred 3 days. The solvent was removed in vacuo, and a yellow solid was precipitated. The solid was suspended in water, stirred overnight at room temperature, filtered, and dried to give 18.6 g (81%) (smaller weight when dried ~ 34%) of the titled compound as a yellow solid: mp 152-154°C; ¹ H NMR (300 MHz, DMSO-d ₆ ) d 4.69 (dd, J = 9.6 Hz, J = 6.7 Hz, 1H, CH at the chiral center), 4.02 (d, J = 11.4 Hz, 1H, CHH _a ), 3.86 (d, J = 11.4 Hz, 1H, CHH _b ), 3.53-3.24 (m, 4H, CH ₂ ), 2.30-2.20 (m, 1H, CH), 2.04-1.72 (m, 3H, CH ₂ and CH), 1.56 (s, 2H, Me); ¹³ C NMR (75 MHz, DMSO-d ₆ ) d 167.3, 163.1, 83.9, 57.2, 45.4, 37.8, 29.0, 22.9, 21.6; IR (KBr) 3474, 1745 (C=0), 1687 (C=0), 1448, 1377, 1360, 1308, 1227, 1159, 1062cm ¹ ; [α] _D ²⁶ +124.5 ⁰ (c = 1.3, chloroform); Anal. Calcd. for C ₉ H ₁₂ BrN0 ₃ : C 41.24, H 4.61, N 5.34. Found: C 41.46, H 4.64, N 5.32.

[000417] (2R)-3-Bromo-2-hydroxy-2-methylpropanoic Acid. A mixture of bromolactone (18.5 g, 71 mmol) in 300 mL of 24% HBr was heated at reflux for 1 h. The resulting solution was diluted with brine (200 mL), and was extracted with ethyl acetate (100 mL x 4). The combined extracts were washed with saturated NaHCO ₃ (100 mL x 4). The aqueous solution was acidified with concentrated HC1 to pH = 1, which, in turn, was extracted with ethyl acetate (100 mL x 4). The combined organic solution was dried over Na ₂ S0 ₄ , filtered through Celite, and evaporated in vacuo to dryness. Recrystallization from toluene afforded 10.2 g (86%) of the desired compound as colorless crystals: mp 107-109°C; ¹ H NMR (300 MHz, DMSO-rfc) d 3.63 (d, J = 10.1 Hz, 1H, CHH _a ), 3.52 (d, J = 10.1 Hz, 1H, CHH _b ), 1.35 (s, 3H, Me); IR (KBr)

3434 (OH), 3300-2500 (COOH), 1730 (C=0), 1449, 1421, 1380, 1292, 1193, 1085 cm ¹ ; [α ]D ²⁶ +10.5° (C = 2.6, MeOH); Anal. Calcd. for C ₄ H ₇ BrO ₃ : C 26.25, H 3.86. Found: C 26.28, H 3.75.

R- 18

[000418] Synthesis of (2R)-3-bromo-N-(3-chloro-4-cyanophenyl)-2-hydroxy-2- methylpropanamide. Thionyl chloride (7.8 g, 65.5 mmol) was added dropwise to a cooled solution (less than 4°C) of (R)-3-bromo-2-hydroxy-2-methylpropanoic acid (9.0 g, 49.2 mmol) in 50 mL of THF under an argon atmosphere. The resulting mixture was stirred for 3 h under the same condition. To this was added Et3N (6.6 g, 65.5 mol) and stirred for 20 min under the same condition. After 20 min, 4-amino-2-chlorobenzonitrile (5.0 g, 32.8 mmol) and 100 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 100 mL of H2O, extracted with EtOAc (2 x 150 mL). The combined organic extracts were washed with saturated NaHCCL solution (2 x 100 mL) and brine (300 mL), successively. The organic layer was dried over MgSCL and concentrated under reduced pressure to give a solid which was purified from column chromatography using EtO Ac/hexane (50:50) to give 7.7 g (49.4%) of target compound as a brown solid.

[000419] ¾ NMR (CDCL/TMS) d 1.7 (s, 3H, CH ₃ ), 3.0 (s, 1H, OH), 3.7 (d, 1H, CH), 4.0 (d, 1H, CH), 7.5 (d, 1H, ArH), 7.7 (d, 1H, ArH), 8.0 (s, 1H, ArH), 8.8 (s, 1H, NH). MS:342.1 (M+23). Mp 129°C. [000420] Synthesis of (S)-/V-(3-chloro-4-cyanophenyl)-3-(4-cyanophenoxy)-2-hydroxy -

2-methylpropanamide (Formula VIII). A mixture of bromoamide (2.0 g, 6.3 mmol), anhydrous K2CO3 (2.6 g, 18.9 mmol) in 50 mL of acetone was heated to reflux for 2 h and then concentrated under reduced pressure to give a solid. The resulting solid was treated with 4-cyanophenol (1.1 g, 9.5 mmol) and anhydrous K2CO3 (1.7 g, 12.6 mmol) in 50 mL of 2- propanol was heated to reflux for 3 h and then concentrated under reduced pressure to give a solid. The residue was treated with 100 mL of H2O and then extracted with EtOAc (2 xlOO mL). The combined EtOAc extracts were washed with 10% NaOH (4 x 100 mL) and brine, successively. The organic layer was dried over MgS04 and then concentrated under reduced pressure to give an oil which was purified by column chromatography using EtO Ac/hexane (50:50) to give a solid. The solid was recrystallized from CH ₂ C1 ₂ /hexane to give 1.4 g (61.6%) of (S)-N-(3-chloro-4-cyanophenyl)-3-(4-cyanophenoxy)-2-hydroxy- 2-methylpropanamide as a colorless solid.

[000421] ¹ H NMR (CDC1 ₃ /TMS) δ 1.61 (s, 3H, CH ₃ ), 3.25 (s, 1H,OH), 4.06 (d, J= 9.15 Hz, 1H, C H), 4.50 (d, J = 9.15 Hz, 1H, C H), 6.97 - 6.99 (m, 2H, Ar H), 7.53-7.59 (m, 4H, Ar H), 7.97 (d, J = 2.01 Hz, 1H, Ar H), 8.96 (s, 1H, N H). Calculated Mass: 355.1, [M+Na] ⁺ 378.0. Mp: 103-105 °C.

EXAMPLE 11

SYNTHESIS OF (S) ENANTIOMER OF FORMULA IX

[000422] Synthesis of (2R)-3-Bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy - 2-methylpropanamide. Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooled solution (less than 4°C) of (R)-3-bromo-2-hydroxy-2-methylpropanoic acid (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. ( R ) - 3 - B ro m o - 2 - h y d ro x y - 2 - methylpropanoic acid was prepared as described in Example 10. The resulting mixture was stirred for 3 h under the same condition. To this was added Et3N (39.14 g, 0.39 mol) and stirred for 20 min under the same condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 300 mL of ¾0, extracted with EtOAc (2 x 400 mL). The combined organic extracts were washed with saturated NaHC0 ₃ solution (2 x 300 mL) and brine (300 mL). The oJganic layer was dried over MgSO4 and concentrated under reduced pressure to give a solid which was purified from column chromatography using CH2C12/EtOAc (80:20) to give a solid. This solid was recrystallized from CH ₂ C1 ₂ /hexane to give 55.8 g (73.9%) of (2R)-3-bromo-/V- [4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropan amide as alight-yellow solid. [000423] ¾ NMR (CDC13/TMS) d 1.66 (s, 3H, C H3), 3.11 (s, 1H, OH), 3.63 (d, J = 10.8 Hz,

1H, C H ₂ ), 4.05 (d, J = 10.8 Hz, 1H, C H ₂ ), 7.85 (d, J= 8.4 Hz, 1H, Ar H), 7.99 (dd, J = 2.1, 8.4 Hz, 1H, Ar H), 8.12 (d, J = 2.1 Hz, 1H, Ar H), 9.04 (bs, 1H, N H). Calculated Mass: 349.99, [M- H]- 349.0. M.p.: 124-126°C.

[000424] Synthesis of (S)-/V-(4-Cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy )- 2-hydroxy-2-methylpropanamide (Formula IX). A mixture of bromoamide ((2R)-3-bromo- A-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylprop anamide, 50 g, 0.14 mol), anhydrous K2CO3 (59.04 g, 0.43 mol), 4-cyanophenol (25.44 g, 0.21 mol) in 500 mL of 2- propanol was heated to reflux for 3 h and then concentrated under reduced pressure to give a solid. The resulting residue was treated with 500 mL of H2O and then extracted with EtOAc (2 x 300 mL). The combined EtOAc extracts were washed with 10% NaOH (4 x 200 mL) and brine. The organic layer was dried over MgS0 ₄ and then concentrated under reduced pressure to give an oil which was treated with 300 mL of ethanol and an activated carbon. The reaction mixture was heated to reflux for 1 h and then the hot mixture was filtered through Celite®. The filtrate was concentrated under reduced pressure to give an oil. This oil was purified by column chromatography using CH ₂ C1 ₂ /EtOAc (80:20) to give an oil which was crystallized from CH ₂ C1 ₂ /hexane to give 33.2 g (59.9%) of (S)-A-(4-cyano-3-(trifluoromethyl)phenyl)-3- (4-cyanophenoxy)-2-hydroxy-2-methylpropanamide as a colorless solid (a cotton type). [000425] ¹ H NMR (CDC13/TMS) d 1.63 (s, 3H, CH ₃ ), 3.35 (s, IH,OH), 4.07 (d, J = 9.04 Hz,

1H, C H), 4.51 (d, J = 9.04 Hz, 1H, C H), 6.97 - 6.99 (m, 2H, Ar H), 7.57-7.60 (m, 2H, Ar H), 7.81 (d, J = 8.55 Hz, 1H, ArH), 7.97 (dd, J = 1.95, 8.55 Hz, 1H, ArH), 8.12 (d, J = 1.95 Hz, 1H, Ar H), 9.13 (bs, 1H, N H). Calculated Mass: 389.10, [M-H] ^“ 388.1. Mp: 92-94°C.

EXAMPLE 12

SYNTHESIS OF (R) ENANTIOMER OF FORMULA IX

[000426] Synthesis of (2S)-3-bromo-/V-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydrox y- 2-methylpropanamide (precursor toR-enantiomer of Formula IX). Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooled solution (less than 4°C) of (S)-3-bromo- 2-hydroxy-2-methylpropanoic acid (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. The resulting mixture was stirred for 3 h under the same condition. To this was added Et3N (39.14 g, 0.39 mol) and stirred for 20 min under the same condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 300 mL of H ₂ 0, extracted with EtOAc (2 X 400 mL). The combined organic extracts were washed with saturated NaHCO ₃ solution

(2 X 300 mL) and brine (300 mL). The organic layer was dried over MgSO ₄ and concentrated under reduced pressure to give a solid which was purified from column chromatography using CH2Cl2/EtOAc (80:20) to give a solid. This solid was recrystallized from EtOAc/hexane to give 55.8 g (73.9%) of target compound as a light-yellow solid. [000427] ¾ NMR (CDC1 ₃ /TMS) d 1.66 (s, 3H, CH ₃ ), 3.11 (s, 1H, OH), 3.63 (d, J= 10.8 Hz,

1H, CH ₂ ), 4.05 (d, J= 10.8 Hz, 1H, CH ₂ ), 7.85 (d, J= 8.4 Hz, 1H, Ar H), 7.99 (dd, J = 2.1, 8.4 Hz, 1H, Ar H), 8.12 (d, J = 2.1 Hz, 1H, Ar H), 9.04 (bs, 1H, N H).

Calculated Mass: 349.99, [M-H] ^“ 349.0. Mp: 124-126°C. [000428] Synthesis of (R)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy) - 2-hydroxy-2-methylpropanamide (R -enantiomer of Formula IX). A mixture of bromoamide (50.0 g, 0.14 mol), anhydrous K2CO3 (59.04 g, 0.43 mol), 4-cyanophenol (25.44 g, 0.21 mol) in 500 mL of 2-propanol was heated to reflux for 3 h and then concentrated under reduced pressure to give a solid. The resulting residue was treated with 500 mL of H2O and then extracted with EtOAc (2 X 300 mL). The combined EtOAc extracts were washed with 10% NaOH (4 X 200 mL) and brine. The organic layer was dried over MgSCL and then concentrated under reduced pressure to give an oil which was treated with 300 mL of ethanol and an activated carbon. The reaction mixture was heated to reflux for 1 h and then the hot mixture was filtered through Celite®. The filtrate was concentrated under reduced pressure to give an oil. This oil was purified by column chromatography using hexane/EtOAc (20:80) to give an oil which was crystallized from EtOAc/hexane to give 33.2 g (59.9%) of (R)-N-( 4- cyano-3-(trifluoromethyl)phenyl)-3-(4-cyanophenoxy)-2-hydrox y-2-methylpropanamide (R- isomer of Formula IX) as a colorless solid. [000429] ₁ H NMR (CDCL/TMS) d 1.63 (s, 3H, C H3), 3.44 (s, IH,OH), 4.07 (d, J= 9.16 Hz,

1H, C H), 4.51 (d, J = 9.16 Hz, 1H, C H), 6.97 - 6.99 (m, 2H, Ar H), 7.57-7.59 (m, 2H, Ar H), 7.81 (d, J = 8.54 Hz, 1H, Ar H), 7.97 (dd, J= 2.07, 8.54 Hz, 1H, Ar H), 8.12 (d, J = 2.07 Hz, 1H, Ar H), 9.15 (bs, 1H, N H). Calculated Mass: 389.10, [M-H] ^“ 388.1. Mp: 92-94°C.

EXAMPLE 13

SYNTHESIS OF (S) ENANTIOMER OF FORMULA X

F ₃ C

[000430] Synthesis of (2R)-3-bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy - 2-methylpropanamide. Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooled solution (less than 4°C) of (R)-3-bromo-2-hydroxy-2-methylpropanoic acid (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. The resulting mixture was stirred for 3 h under the same condition. To this was added Et3N (39.14 g, 0.39 mol) and stirred for 20 min under the same condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 300 mL of H2O, extracted with EtOAc (2 X 400 mL). The combined organic extracts were washed with saturated NaHCO3 solution (2 X 300 mL) and brine (300 mL). The organic layer was dried over MgSO ₄ and concentrated under reduced pressure to give a solid which was purified by column chromatography using CH ₂ C1 ₂ /EtOAc (80:20) to give a solid. This solid was recrystallized from CH ₂ C1 ₂ /hexane to give a target compound (55.8 g, 73.9%) as a light- yellow solid.

[000431] ₁ H NMR (CDC13/TMS) d 1.66 (s, 3H, CH ₃ ), 3.11 (s, 1H, OH), 3.63 (d, J = 10.8 Hz, 1H, C H ₂ ), 4.05 (d, J = 10.8 Hz, 1H, C H ₂ ), 7.85 (d, J= 8.4 Hz, 1H, Ar H), 7.99 (dd, J = 2.1, 8.4 Hz, 1H, Ar H), 8.12 (d, J = 2.1 Hz, 1H, Ar H), 9.04 (bs, 1H, N H). Calculated Mass: 349.99, [M-

H]- 349.0. Mp: 124-126°C.

[000432] Synthesis of (S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluorophenoxy )- 2-hydroxy-2-methylpropanamide (Formula X). A mixture of bromoamide (10.0 g, 28.5 mmol), anhydrous K2CO3 (11.8 g, 85.4 mmol) in 150 mL of acetone was heated to reflux for 1 h and then concentrated under reduced pressure to give a solid. The resulting residue was treated with 4-fluorophenol (4.8 g, 42.7 mmol), anhydrous K2CO3 (7.9 g, 57.0 mmol), 150 mL of 2-propanol and then heated to reflux for 2 h. The resulting mixture was concentrated under reduced pressure to give a solid. This solid was treated with 300 mL of H2O and extracted with EtOAc (2 X 250 mL). The combined EtOAc extracts were washed with a saturated NaHC0 ₃ solution (2 X 250 mL) and brine. The organic layer was dried over MgS0 ₄ and then concentrated under reduced pressure to give an oil which was purified by column chromatography using CH2Cl2/EtOAc (80:20) to give a solid. This solid was recrystallized from CH2Cl2/hexane to give (S)-A-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-fluorophenoxy )- 2-hydroxy-2-methylpropanamide (Lormula X, 10.04 g, 92.2%) as a colorless solid.

[000433] ¾ NMR (CDCb/TMS) d 1.59 (s, 3H, C H ₃ ), 3.36 (s, IH,OH), 3.95 (d, J= 9.00 Hz, 1H, C H), 4.43 (d, J = 9.00 Hz, 1H, C H), 6.87-6.88 (m, 2H, Ar H), 6.96-7.02 (m, 2H, Ar H), 7.81 (d, J= 8.45 Hz, 1H, Ar H), 7.94-7.98 (m, 1H, Ar H), 8.10 (d, J= 1.79 Hz, 1H, Ar H), 9.11 (s, 1H, N H). Calculated Mass: 382.31, [M-H] ^“ 380.9. Mp: 139-141°C.

EXAMPLE 14

SYNTHESIS OF (S) ENANTIOMER OF FORMULA XIII

R- 19

[000434] Synthesis of (2R)-3-Bromo-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy - 2-methylpropanamide. Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooled solution (less than 4°C) of R-18 (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. R-18 is (R)-3-bromo-2-hydroxy-2-methylpropanoic acid was prepared as described in Example 10. The resulting mixture was stirred for 3 h under the same condition. To this was added Et3N (39.14 g, 0.39 mol) and stirred for 20 min under the same condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 300 mL of H2O, extracted with EtOAc (2 x 400 mL). The combined organic extracts were washed with saturated NaHCO ₃ solution (2 x 300 mL) and brine (300 mL). The organic layer was dried over MgSCri and concentrated under reduced pressure to give a solid which was purified from column chromatography using CH2Cl2/EtOAc (80:20) to give a solid. This solid was recrystallized from CH2C12/hexane to give 55.8 g (73.9%) of (2R)-3-bromo-A-[4-cyano-3- (trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide (R-19) as a light-yellow solid.

[000435] ₁ H NMR (CDC1 ₃ /TMS) d 1.66 (s, 3H, C H ₃ ), 3.11 (s, 1H, OH), 3.63 (d, 7 = 10.8 Hz, 1H, CH2), 4.05 (d, 7 = 10.8 Hz, 1H, CH2), 7.85 (d, 7= 8.4 Hz, 1H, ArH), 7.99 (dd, 7 = 2.1, 8.4 Hz, 1H, ArH), 8.12 (d, 7 = 2.1 Hz, 1H, ArH), 9.04 (bs, 1H, N H). Calculated Mass: 349.99, [M- H]- 349.0. M.p.: 124-126°C.

R- 19

[000436] Synthesis of (S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyano-3- fluorophenoxy)-2-hydroxy-2-methylpropanamide (Formula XIII). A mixture of bromoamide ((2R)-3-bromo-A-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydrox y-2- methylpropanamide R- 19 (2.0 g, 5.70 mmol)), anhydrous K ₃ C0 ₃ (2.4 g, 17.1 mmol) in 50 mL of acetone was heated to reflux for 2 h and then concentrated under reduced pressure to give a solid. The resulting solid was treated with 2-fluoro-4-hydroxybenzonitrile (1.2 g, 8.5 mmol) and anhydrous K ₃ C0 ₃ (1.6 g, 11.4 mmol) in 50 mL of 2-propanol was heated to reflux for 3 h and then concentrated under reduced pressure to give a solid. The residue was treated with 100 mL of H2O and then extracted with EtOAc (2 x 100 mL). The combined EtOAc extracts were washed with 10% NaOH (4 x 100 mL) and brine, successively. The organic layer was dried over MgSO ₄ and then concentrated under reduced pressure to give an oil which was crystallized from CH ₂ C1 ₂ hexane to give 0.5 g (23%) of (S)-N-(4-cyano-3- (trifluoromethyl)phenyl)-3-(4-cyano-3-fluorophenoxy)-2-hydro xy-2-methylpropanamide as a colorless solid.

[000437] ₁ H NMR (CDC1 ₃ /TMS) d 1.63 (s, 3H, C H ₃ ), 3.34 (bs, 1H,OH), 4.08 (d, J = 9.17

Hz, 1H, C H), 4.50 (d, J = 9.17 Hz, 1H, C H), 6.14 - 6.82 (m, 2H, Ar H), 7.50-7.55 (m, 1H,

Ar H), 7.81 (d, J = 8.50 Hz, 1H, Ar H), 7.97 (q, J = 2.03, 8.50 Hz, 1H, Ar H), 8.11 (d, J = 2.03 Hz, 1H, Ar H), 9.12 (s, 1H, N H). Calculated Mass: 407.1, [M+Na] ⁺ 430.0. Mp: 124-125°C.

EXAMPLE 15

SYNTHESIS OF (S) ENANTIOMER OF FORMULA XIY

(R)-3-bromo-2-hydroxy-2- methylpropanoic acid

R- 18

R- 19

[000438] Synthesis of (2R)-3-Bromo-/V-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydrox y- 2-methylpropanamide. Thionyl chloride (46.02 g, 0.39 mol) was added dropwise to a cooled solution (less than 4°C) of R-18 (51.13 g, 0.28 mol) in 300 mL of THF under an argon atmosphere. R-18 is (R)-3-bromo-2-hydroxy-2-methylpropanoic acid was prepared as described in Example 10. The resulting mixture was stirred for 3 h under the same condition. To this was added Et N (39.14 g, 0.39 mol) and stirred for 20 min under the same condition. After 20 min, 5-amino-2-cyanobenzotrifluoride (40.0 g, 0.21 mol), 400 mL of THF were added and then the mixture was allowed to stir overnight at room temperature. The solvent was removed under reduced pressure to give a solid which was treated with 300 mL of ¾0, extracted with EtOAc (2 X 400 mL). The combined organic extracts were washed with saturated NaHCCL solution (2 X 300 mL) and brine (300 mL). The organic layer was dried over MgSCL and concentrated under reduced pressure to give a solid, which was purified from column chromatography using CH Cl /EtOAc (80:20) to give a solid. This solid was recrystallized from CH2C12/hexane to give 55.8 g (73.9%) of ( 2 R ) - 3 - b ro m o - N - [ 4 - c y a n o - 3 - (trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide (R-19) as a light-yellow solid.

[000439] ¾ NMR (CDC13/TMS) d 1.66 (s, 3H, CH ₃ ), 3.11 (s, 1H, OH), 3.63 (d, J= 10.8 Hz, 1H, C H ₂ ), 4.05 (d, J= 10.8 Hz, 1H, C H ₂ ), 7.85 (d, J= 8.4 Hz, 1H, Ar H), 7.99 (dd, J = 2.1, 8.4 Hz, 1H, Ar H), 8.12 (d, J = 2.1 Hz, 1H, Ar H), 9.04 (bs, 1H, N H). Calculated Mass: 349.99, [M-

H]- 349.0. M.p.: 124-126°C.

R- 19

[000440] Synthesis of (S)-3-(4-chloro-3-fluorophenoxy)-/V-(4-cyano-3- (trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide (Formula XIV)

[000441] A mixture of bromoamide ((2R)-3-bromo-A-[4-cyano-3-(trifluoromethyl)phenyl]- 2-hydroxy-2-methylpropanamide (R-19) 2.0 g, 5.70 mmol)), anhydrous K ₂ CO ₃ (2.4 g, 17.1 mmol) was heated to reflux for 2 h and then concentrated under reduced pressure to give a solid. The resulting solid was treated with 4-chloro-3-fluorophenol (1.3 g, 8.5 mmol) and anhydrous K2CO3 (1.6 g, 11.4 mmol) in 50 mL of 2-propanol was heated to reflux for 3 h and then concentrated under reduced pressure to give a solid. The residue was treated with 100 mL of H2O and then extracted with EtOAc (2 X 100 mL). The combined EtOAc extracts were washed with 10% NaOH (4 X 100 mL) and brine, successively. The organic layer was dried over MgSO ₄ and then concentrated under reduced pressure to give an oil which was purified by column chromatography using EtOAc/hexane (50:50) to give a solid which was recrystallized from CH ₂ C1 ₂ /hexane to give 1.7 g (70.5%) of (5)-3-(4-chloro-3-fluorophenoxy)- iV-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpro panamide as a colorless solid.

[000442] ₁ H NMR (CDC1 ₃ /TMS) d 1.60 (s, 3H, CH ₃ ), 3.28 (s, 1H, OH), 3.98 (d, J = 9.05 Hz, 1H, C H), 6.64 - 6.76 (m, 2H, Ar H), 7.30 (d, J= 8.67 Hz, 1H, Ar H), 7.81 (d, J= 8.52 Hz, 1H, ArH), 7.96 (q, J = 2.07, 8.52 Hz, 1H, Ar H), 8.10 (d, J= 2.07 Hz, 1H, Ar H), 9.10 (s, 1H, N H). Calculated Mass: [M-H] ^“ 414.9. Mp: 132-134°C.

EXAMPLE 16

BINDING AND TRANSACTIVATION OF SARMS IN BREAST CANCER CELLS

[000443] In order to determine whether SARM compounds as described herein are agonists in breast cancer cells, HEK-293 or MDA-MB-231 cells were transfected with 0.25 pg GRE- LUC, 10 ng CMV-renilla LUC, and 25 ng CMV-hAR using lipofectamine. Twenty four hours after transfection, the cells were treated with DHT, compound of Formula VIII or compound of Formula IX and luciferase assay was performed 48 hrs after transfection. Competitive binding of DHT, compound of Formula VIII and compound of Formula IX were measured using an in vitro competitive radioligand binding assay with [ 17α-methyl-3H ]-miholerone ([ ³ H]MIB), a known steroidal and high affinity AR ligand, and purified AR-LBD protein.

Results:

[000444] DHT, compound of Formula VIII and Formula IX are agonists of AR in breast cancer cells as presented in Figure 13A-13C (HEK-293 cells in Figure 13 A and MDA-MB- 231 cells in Figures 13B-13C). The relative binding affinities (RBAs) for AR of DHT, Formula IX, Formula VIII, and bicalutamide were 1.0, 0.330, 0.314, and 0.016, respectively, demonstrating high affinity AR binding for the SARM SARM compounds as described herein (data not shown). EXAMPLE 17

INHIBITION OF INTRATUMORAL GENE EXPRESSION

[000445] AR agonists differentially regulate genes in ER-positive and ER- negative breast cancer cells. MDA-MB-231 and MCF-7 cells infected with AR or GFP containing adenovirus were maintained in charcoal stripped serum containing medium for 3 days and were treated with DHT or Formula VIII. After overnight treatment, the cells were harvested, RNA isolated and real-time PCR for the indicated genes were performed. The expression of various genes in response to either DHT or Formula VIII were measured and normalized to GAPDH, and are presented as composite data (same effects for DHT and Formula VIII) in Table 6. [000446] Table 6: Differential Regulation of Gene Expression by AR Figands in ER-

Positive (MCF7) and ER-Negative (MDA-MB-231) Breast Cancers

VCAM1 - Vascular cell adhesion protein- 1 - Important for anchorage-dependent growth of cells and also is a chemoattractant. SPARC - Secreted protein acidic and rich in cysteine (aka Osteonectin) - extracellular glycoprotein important for angiogenesis.

MUC1 - Mucinl - Extracellular glycoprotein associated with cancers - Its promoter has a strong ARE.

SLUG - Zinc finger transcription factor - Its promoter has a strong ARE. MMP2 - matrix metalloproteinase-2 - gene that is activated by cell-cell clustering. EXAMPLE 18

GENE EXPRESSION ARRAY OF MDA-MB-231-AR XENOGRAFT

[000447] RNA was extracted from MDA-MB-231-AR tumors (n=5/group) treated with vehicle or compound of Formula VIII. RNA was pooled and Affymetrix microarray was performed to determine the change in expression of gene signature.

RESULTS

[000448] The results presented in Figure 15 show that activation of AR in MDA-MB-231- AR xenografts suppressed the expression of more genes than it induced in these tumors. This pattern is unique in breast cancer cells and is different from gene expression results observed in prostate cancer cells, where more genes are induced than repressed (data not shown).

[000449] The results presented in Figure 16 validate the microarray results presented in Figure 15 by analyzing selected genes using realtime PCR TaqMan primers and probe in ABI 7900. EXAMPLE 19

FORMULA VIII INHIBITS THE GROWTH OF MCF-7-AR XENOGRAFT

[000450] MCF-7 cells stably transfected with AR using lentivirus were implanted (2 million cells/mouse; n=5) in nude mice that were ovariectomized and supplemented with 17 b-eslradiol (50 μg/day). Once tumors reached 100-200 mm ³ , the animals were randomized and treated with vehicle or 30 mg/kg per day of Formula VIII. Tumor volumes and body weights were measured thrice weekly. At the end of 5 weeks of treatment, the animals were sacrificed, tumors weighed and stored for RNA and protein isolation and histology. * significance at P<0.05.

[000451] In addition, uterus weights were measured in these xenograft studies, and Western blot from MCF-7 tumor xenografts were probed for AR.

RESULTS

[000452] The graph presented in Figure 17 demonstrates inhibition of triple-positive breast cancer (ER, PR, and HER2) using Formula VIII. The results show that Formula VIII inhibited the growth of MCF-7 breast cancer cell xenografts by greater than 50%.

[000453] The results presented in Figure 18 show Formula VIII inhibited uterus weight in these estrogen supplemented animals.

[000454] The results presented in Figure 19 demonstrate that the AR expression pattern in response to agonist (Formula VIII) is similar to that observed in prostate cancer cells (data not shown).

EXAMPLE 20

FORMULA VIII UP-REGULATES JNK PHOSPHORYLATION IN MCF7-AR

TUMORS [000455] Protein from MCF-7-AR tumors that were treated with vehicle or compound of

Formula VIII were extracted and incubated with phospho MAPK array to determine the effect of compound of Formula VIII on phosphorylation of various kinases.

RESULTS

[000456] The results presented in Figure 21 show that JNK phosphorylation is upregulated in MCF-7-AR tumors by treatment with compound of Formula VIII. JNK plays a critical role in death receptor- mediated intrinsic and extrinsic apoptotic pathways. JNK activates apoptotic signaling by up-regulating pro-apoptotic genes. The observed phosphorylation of the pro- apoptotic kinase, JNK, may be suggestive of a possible mechanistic explanation of the anti- proliferation.

EXAMPLE 21

GENE EXPRESSION ANALYSIS OF MDA-MB-231-AR AND MCF-7-AR XENOGRAFTS FOLLOWING TREATMENT WITH FORMULA VIII AND

FORMULA IX

[000457] Microarray Analysis was performed on RNA from MDA-MB-231-AR and MCF-7- AR tumors in order to identify and compare changes in gene expression in ER-negative (MDA- MB-231-AR; triple negative) an ER-positive (MCF-7-AR; triple positive) breast cancer tumors treated with a compound of Formula VIII (30 mg/kg/day p.o. for 4 weeks). Affymetrix analysis of the xenografts was done on pooled samples of the xenografts. The analysis included -70,000 sequences with -30,000 genes and variations thereof represented, as well as microRNA’s. RNA was isolated and expression of genes was evaluated using microarray (Affymetrix Human Gene ST 2.0 array). Expression of genes in compound of Formula VIII- treated samples was compared with the expression in vehicle-treated samples. Genes that were up- or down- regulated by more than 2 fold were considered differentially regulated by compound of Formula VIII.

RESULTS

[000458] Table 7 below presents the sum totals of up-regulated and down-regulated genes in MDA-MB-231-AR and MCF-7-AR tumors [000459] Table 7:

[000460] Of particular interest was that of the 1547 regulated genes identified in MCF-7- AR tumors and the 1536 regulated genes identified in MDA-MB-231-AR tumors, the subset of overlapping genes was only 245 genes. This result indicated that Formula VIII regulated distinct sets of genes in MCF-7-AR (ER-positive; triple positive) and MDA-MB-231-AR (ER- negative; triple negative) breast cancer cells.

[000461] Tables 8 and 9 below present genes involved in mammary tumorigenesis that were differentially regulated (by at least 2 fold) by Formula VIII in MDA-MB-231-AR tumors (Table 8) and MCF-7-AR tumors (Table 9). Indications of up-regulation or down-regulation are presented in the right-most column.

[000462]Table 8: Breast cancer relevant genes modulated in MDA-MB-231-AR tumors

[000463] Table 9: Breast cancer relevant genes modulated in MCF-7-AR tumors [000464] The results presented in Tables 7 and 8 show that SARM treatment (Formula VIII) caused net down-regulation of genes in MDA-MB-231-AR tumors (N =1042 suppressed; N = 640 induced; threshold of 2-2.5-fold increase or decrease (note: plot is log of fold change; follow-up RT-PCR demonstrated 10-20-fold changes). Well known androgen-dependent genes (e.g., FKP5 and MUC1 ; See Table 10 below) were elevated, showing SARM penetration into the tumor. Also 29/36 known breast cancer-related genes were shown to be decreased, supporting a rational basis for the anti-proliferation activity of Formula VIII in ER-negative breast cancer. [000465] Further analysis of the results in MDA-MB-231-AR tumors showed that Formula

VIII induced known androgen-responsive genes (Table 10 below). Thus, breast cancer relevant genes such as beta2- adrenergic receptor and PARP1 were suppressed by Formula VIII; whereas ARE-dependent genes were induced by treatment of Formula VIII.

[000466] Table 10

[000467] The results presented in Tables 7 and 9 show that Formula VIII did not have as strong of a gene suppressive tone in MCF-7-AR triple positive (ER-positive) tumors as in triple negative (ER-negative) tumors. Interestingly though, the MCF-7-AR analysis showed that androgen-dependent genes were up regulated and estrogen-dependent genes were suppressed (Table 11 below), as validated by RT-PCR.

[000468] Table 11 [000469] The results presented in Figure 20 validate the microarray results presented in the above analyses, by analyzing selected genes using realtime PCR TaqMan primers and probe in ABI 7900. [000470] The results presented in Figure 22 show inhibition of triple negative breast cancer growth using Formulae VIII and IX. Formula VIII and Formula IX demonstrated -85% TGI at all doses tried (5, 10 mg per kg for Formula VIII; 5, 10, 30 mg per kg for Formula IX) in the triple negative breast cancer model using MDA-MB-231-AR cells in nude mice.

[000471] The results presented in Figure 23 demonstrate inhibition of triple negative breast cancer using Formulae VIII and IX. Tumor weights were likewise reduced for all doses of Formula VIII and Formula IX. Spleen enlargement (680 mg vs. 200-300 mg for normal mice) was seen only in vehicle treated mice, possibly indicative of prevention by the SARMs of tumor metastasis to the spleen.

[000472] The in vitro data shown in MCF-7 cells with and without AR (Figures 25A-25E) support that SARM-activated AR may sequester the co-factors that are used by ER. Adding AR to the MCF-7 cells increased the effect of 17 b-estradiol (when unopposed) on the ER target genes PR and pS2, but the antagonism caused by SARM alone or SARM + 17 b-estradiol (E2) was enhanced in this setting (Figures 25B and 25D) as compared to GFP (i.e. no AR; Figures 25A and 25C). Figure 25E shows that AR target genes are enhanced by SARM even in the presence of 17 b-estradiol .

EXAMPLE 22

XENOGRAFT EXPERIMENT WITH FORMULA IX

[000473] Xenograft experiment. NSG mice obtained from JAX labs were housed with five animals per cage and were allowed free access to tap water and commercial rat chow (Harlan Teklad 22/5 rodent diet - 8640). During the course of the study, the animals were maintained on a 12 hr light:dark cycle. Animals were anesthetized and BR-0001 TNBC fragments of 1 mm ³ (approximately) were implanted subcutaneously in NSG mice. Once the tumor size reached 100-200 mm ³ , the animals were randomized and treated with vehicle control (polyethylene glycol:DMSO 9:1 ratio) or 10 mg/kg/day Formula IX (n=12) or enzalutamide orally. Tumor volume was measured thrice weekly. Tumor volume was calculated using the formula lengthxwidthxwidthxO.5236. Once tumors reached greater than 1500-2000 mm ³ , animals were sacrificed and tumors weighted and stored for various analysis. Two regions of the same BR-0001 tumor, an AR-positive TNBC xenograft, were immunohistochemically stained with AR antibody (AR N20 from SCBT) (Figures 26A and 26B) and compared to an AR-negative (Figure 26C) TNBC as a negative control. Figures 26A and 26B show that AR expression is consistent throughout this formalin-fixed, paraffin-embedded (FFPE) tissue, whereas similar FFPE in AR-negative TNBC demonstrated no staining (no AR expression). The tumor xenograft efficacy experimental results are provided in 27A-27C, with Figures 27A and 27B being replicate experiments. Formula IX (lower trace) produced some tumor growth inhibition of this AR-positive TNBC tumor in each experiment whereas enzalutamide was indistinguishable from vehicle treatment (Figures 26A and 26B). Formula IX reduced tumor weight in experiment 2 by -40%.

EXAMPLE 23

Ki-67 STAINING WAS REDUCED IN AR-POSITIVE TNBC TUMORS OF ANIMALS TREATED WITH FORMULA IX

[000474] Figures 28A-28B demonstrated an approximately 50% reduction in Ki-67 staining in 2 weeks of treatment. Tumors from replicate experiment 2 (Figure 27B) were fixed in formalin and paraffin embedded. Slides were cut and stained with Ki-67 antibody. Ki-67 positive cells (total 200 cells were counted in each slide) in each slide were counted and represented as % stained cells, as shown in Figure 28B. Ki-67 staining was reduced in tumors of the animals treated with Formula IX.

EXAMPLE 24

GENE EXPRESSION STUDY AND ChIP-SEQ STUDY IN AR-POSITIVE TNBC

TUMOR XENOGRAFTS

Methods

[000475] Chromatin Immunoprecipitation Assay ( ChIP ). Proteins were cross-linked by incubation with 1% formaldehyde (final concentration) at 37°C for 10 min. Tumors were homogenized using a probe hand-held homogenizer. The cells were washed with lx PBS twice, scraped in 1 mL of PBS containing protease inhibitors ([1 mg each of aprotinin, leupeptin, antipain, benzamidine HC1, and pepstatin/mL], 0.2 mM phenylmethylsulfonyl fluoride, and 1 mM sodium vanadate), pelleted, and resuspended in SDS lysis buffer (1% SDS, 10 mM EDTA, 50 mM Tris-HCl [pH 8.1]).

[000476] After lysis on ice for 10 min, the cell extract was sonicated (Branson sonifier 250) in a cold room eight times for 10 s each at constant duty cycle, with an output of 3 and with incubation on ice after every sonication. The debris was pelleted at 13,000 rpm for 10 min at 4°C, and the supernatant was diluted 10-fold with ChIP dilution buffer (0.01% SDS, 1.1% Triton X-100, 1.2 mM EDTA, 16.7 mM Tris HC1 [pH 8.1], 167 mM NaCl). The proteins were precleared with 50 pL of 1:1 protein A-Sepharose beads in TE. An aliquot (300 pL) was reserved as input, while the remaining solution was incubated with 5 pg of AR antibody (AR N20 SCBT) and 2 pg of sheared salmon sperm DNA (Stratagene, La Jolla, CA) rotating overnight at 4°C.

[000477] The protein-DNA-antibody complex was precipitated by incubating with 100 pL of 1:1 protein A-Sepharose beads and 2 pg of salmon sperm DNA at 4°C for 2 h. The beads were pelleted and washed three times with low-salt wash buffer (0.1% sodium dodecyl sulfate [SDS], 1% Triton X-100, 2 mM EDTA, 20 mM Tris HC1 [pH 8.1], 0.15 M NaCl), and twice with lx TE (10 mM Tris HC1, 1 mM EDTA; pH 8.0). DNA-protein complexes were obtained by extracting the beads with 50 pL of freshly prepared extraction buffer (1% SDS, 0.1 M NaHCCb) three times. Cross-linking of the DNA protein complexes was reversed by incubating at 65 °C for 6 h. The DNA was extracted with a QIAquick PCR purification kit (QIAGEN, Valencia, Calif.) in 25 pL final volume of TE. The purified DNA was given to University of Tennessee Health Science Center Molecular Resource Center (UTHSC MRC) for next generation sequencing using ion proton sequencer.

[000478] RNA Analysis and microarray. Tumors were homogenized, RNA isolated, purified and submitted to the UTHSC MRC core facility for microarray analysis (ST2.0 array from Affymetrix).

Results

[000479] In the gene expression study described above, RNA was isolated from the BR-0001 TNBC tumors and the expression of genes in the entire genome was measured by microarray (Affymetrix, ST2.0 array). In the ChIP-Seq study, chromatin immunoprecipitation was performed in untreated BR-0001 specimen and the DNA immunoprecipitated with AR antibody was sequenced using ion torrent next-generation sequencer. It was shown that -20% of AR-occupied promoters (-5kb to +1 kb) were activated by androgen (mRNA increased by >1.5 fold) (data not shown). Androgen treatment primarily affected cell cycle and metabolic process according to gene set enrichment analysis (GSEA) (Figure 31). Expression of TNBC subtype markers in Figures 30A and 30B show that in the SARM-treated tumors, gene markers for LAR and MSL subtypes are highly expressed.

[000480] Gene expression data was compared to PAM50 to determine the tumor type that BR- 0001 belonged to. The expression (Z-score) of 50 genes required to classify the breast cancer is given in Figure 29, in which PAM50 indicated that the tumor belonged to basal-like breast cancer (BFBC) TNBC.

[000481] Triple-negative breast cancer (TNBC) is a heterogeneous breast cancer group, and identification of its subtypes is essential for understanding the biological characteristics and clinical behaviors of TNBC as well as for developing personalized treatments. Based on 3,247 gene expression profiles from 21 breast cancer data sets, six TNBC subtypes, including 2 basal- like (BF1 and BF2), an immunomodulatory (IM), a mesenchymal (M), a mesenchymal stem like (MSF), and a luminal androgen receptor (FAR) subtype from 587 TNBC samples with unique gene expression patterns and ontologies, were discovered (Brian D. Lehman et ai, J. Clin. Invest. 2011, 121(7), 2750-2767). Cell line models representing each of the TNBC subtypes also displayed different sensitivities to targeted therapeutic agents. Gene expression data was compared to the genes published (Pietenpol group) to classify the BLBC into sub- classification. Figures 30A-30B depict that Pietenpol classification of TNBC suggests that the BR-0001 tumor is LAR and MSL subtypes.

EXAMPLE 25

GENE EXPRESSION CHANGES IN AR-POSITIVE TNBC XENOGRAFT TUMORS

[000482] Figure 31 demonstrates that in BR-0001 tumors Formula IX up-regulated gene expression. Approximately 4200 genes were up-regulated by Formula IX compared to vehicle, while approximately 1170 genes were down-regulated by Formula IX compared to vehicle. Formula IX recruited AR to 176 promoters (-5 kb to +1 kb). 20% of the promoters occupied by the AR in response to Formula IX also had the gene up-regulated by Formula IX. This showed that these genes were direct targets of the AR rather than an indirect effect. The Ingenuity Pathway Analysis (http://www.ingenuity.com/; QIAGEN, Redwood City, California) suggests that genes involved in cell cycle were altered by Formula IX. EXAMPLE 26

THE EFFICACY AND SAFETY OF FORMULA IX ON ADVANCED, ANDROGEN RECEPTOR-POSITIVE TRIPLE NEGATIVE BREAST CANCER (AR+ TNBC)

[000483] Ongoing and Completed Clinical Trials with Formula IX: Twenty-one Phase 1, 2, and 3 clinical trials have been completed or are ongoing with Formula IX. These include: 1. Protocol G100401, a Phase 1 single ascending dose study in 96 healthy, young, male volunteers; 2. Protocol G100402, a Phase 1 multiple ascending dose study in 50 healthy, young, male volunteers, and 23 elderly male volunteers with truncal obesity; 3. Protocol G100503, a Phase 1 single dose pharmacokinetic study to assess the effect of a dosage regimen that simulates a sustained release formulation to an immediate release formulation in 18 healthy, young male volunteers and 18 postmenopausal women; 4. Protocol G100506, a Phase 1 single dose pharmacokinetic study to assess the relative bioavailability of a 3 mg hard shell capsule formulation to be used during continued clinical development and to assess the effect of food on the pharmacokinetics of the 3 mg softgel formulation in 27 healthy, young, male volunteers; 5. Protocol 006, a Phase 1 single dose and multiple dose pharmacokinetic study in 24 postmenopausal, Japanese women; 6. Protocol G200501, a Phase 2 study in 60 postmenopausal women and 60 elderly men to assess lean body mass and physical function; 7. Protocol 003, a Phase lb study in 44 postmenopausal women; 8. Protocol G200502, a Phase 2b study in 159 men and postmenopausal women with cancer to assess lean body mass and physical function; 9. Protocol G100511, a Phase 1 study to assess the effect of severe renal impairment on the pharmacokinetics of Formula IX; 10. Protocol G100508, a Phase 1 study to assess the effect of mild and moderate hepatic impairment on the pharmacokinetics of Formula IX; 11. Protocol G100509, a Phase 1 mass balance study of Formula IX in healthy volunteers; 12. Protocol G100507, a Phase 1 study to assess the pharmacokinetics and absolute oral bioavailability of Formula IX in Caucasian and African American men and women; 13. Protocol G100510, a single-dose, randomized, double-blind, comparative, positive and placebo-controlled, four-period crossover Phase 1 study to define the electrocardiogram (ECG) effects of Formula IX, at therapeutic and supratherapeutic doses, in healthy male and female subjects: a thorough ECG trial; 14. Protocol G100512, a Phase 1 study to assess the effect of ketoconazole (Cytochrome P450, Family 3, Subfamily A [CYP3A4] inhibitor) on the pharmacokinetics of Formula IX; 15. Protocol G100513, a Phase 1 study to assess the effect of rifampin (CYP3A4 inducer) on the pharmacokinetics of Formula IX; 16. Protocol G100514, a Phase 1 study to assess the pharmacokinetic drug:drug interaction of Formula IX and celecoxib (CYP2C9); 17. Protocol G100515, a Phase 1 study to assess the pharmacokinetic drug:drug interaction of Formula IX and probenecid (UGT2B7); 18. Protocol G100516, a Phase 1 study to assess the pharmacokinetic drug:drug interaction of Formula IX and rosuvastatin (breast cancer resistance protein [BCRP]); 19. Protocol G300504, a Phase 3 randomized, double-blind, placebo-controlled study of the effect of Formula IX on muscle wasting in 321 subjects with non-small cell lung cancer receiving first line platinum plus a taxane chemotherapy; 20. Protocol G300505, a Phase 3 randomized, double-blind, placebo-controlled study of the effect of Formula IX on muscle wasting in 320 subjects with non-small cell lung cancer receiving first line platinum plus a non-taxane chemotherapy; 21. Protocol G200801, an ongoing, Phase 2, open label study to examine AR status and the activity of Formula IX hormonal therapy in 22 women with ER-positive metastatic breast cancer who have previously responded to hormone therapy.

[000484] The 18 mg dose: Formula IX has been evaluated in 21 completed and ongoing clinical studies enrolling over 1,500 total subjects. Formula IX has been generally well- tolerated, including single doses up to 100 mg and multiple doses up to 30 mg once daily for up to 14 days. In longer studies, Formula IX has also been generally well tolerated, including 1, 3, and 9 mg daily doses for up to 184 days.

[000485] Previous clinical studies demonstrated that daily doses up to 30 mg of Formula IX were well tolerated in healthy male volunteers. Both 10 mg and 30 mg daily doses were evaluated in Protocol G100402 for up to 14 days. Elevated alanine transaminase (ALT) (any elevation outside upper limit of normal [ULN]) was the most common adverse event (AE) experienced. None of the subjects in the 10 mg dose group were discontinued from the study due to ALT elevations. In the 30 mg dose group, six subjects experienced ALT increases above two times the ULN.

[000486] Formula IX 3 mg given daily was evaluated in two completed Phase 3 trials, in over 600 subjects, for the prevention and treatment of muscle wasting (cachexia) in subjects with advanced non-small cell lung cancer receiving chemotherapy. Formula IX 3 mg increased lean body mass in both studies and was safe and well tolerated when dosed for up to 168 days. Subjects in the Formula IX and placebo groups experienced similar AEs and these AEs were consistent with the background chemotherapy regimen. [000487] Although Formula IX 3 mg was chosen for its anabolic activity in muscle for the completed Phase 3 program, a dose of 9 mg once daily was selected for hormonal therapy in the ongoing Phase 2 trial in ER+ and AR+ metastatic breast cancer in order to achieve a higher exposure that is both safe and more likely to be efficacious in women with advanced breast cancer. Seven out of twenty-two subjects with advanced, heavily pretreated (hormonal therapy, radiation, and chemotherapy) breast cancer demonstrated clinical benefit (CB) (stable disease [SD]) at 6 months. In one subject with SD (by Response Evaluation Criteria in Solid Tumors [RECIST], Version 1.12), tumor regression of 27% was demonstrated. Consistent with the previous studies, Formula IX remained safe and well tolerated (see Example 9).

[000488] Reductions in sex hormone binding globulin (SHBG) have been identified as one of the most sensitive serum biomarkers for AR signaling in healthy volunteers and patients. SHBG was reduced by 15.1%, 15.6%, 18.2%, and 18.4% in young, healthy volunteers who received PO Formula IX 1 mg, 3 mg, 10 mg, and 30 mg daily for 14 days, respectively, in Protocol G100402 (listed as trial #2 above), suggesting that doses of 10 mg and above maximally stimulate AR activity.

[000489] Dosing Formula IX at 15-20 mg per day may provide therapeutic benefit in hormone receptor positive breast cancer by two separate mechanisms: activating AR and inhibiting progesterone receptor, thereby increasing potential efficacy. Progesterone receptor expression in cancer stem cells has been shown to be involved in proliferation of cancer epithelial cells, and inhibiting progesterone receptor’s activity is now considered a novel approach to treating breast cancer. Hence, Formula IX at higher doses might provide dual anti- proliferative effects in breast cancer. In TNBC, doses of 15-20 mg per day should provide saturation of the AR potentially providing better efficacy as opposed to a lower dose with partial occupancy of the AR and absence of any progesterone receptor inhibitory effect.

[000490] Based on the safety data collected to date in both preclinical and clinical settings, the 18 mg dose is expected to be safe and generally well tolerated. However, in the event that a subject has a Grade 3 or greater toxicity, the 18 mg dose may be reduced to 9 mg until the AE resolves or for the remainder of treatment based on the Investigator’s discretion. The 9 mg dose has been previously studied in postmenopausal women with metastatic breast cancer and was safe and well tolerated. [000491] In TNBC patients, the 18 mg dose is preferred over a lower dose due to the aggressive phenotype of the disease and poor prognosis. Based on preclinical data, the 18 mg dose is more likely to saturate the AR and may lead to better clinical outcomes than a lower dose without receptor saturation or progesterone receptor inhibition.

[000492] The 18 mg dose may provide greater efficacy in TNBC without compromising subject safety. However, in the event that a subject has a Grade 3 or greater toxicity, the 18 mg dose may be reduced to 9 mg until the AE resolves or for the remainder of treatment based on the Investigator’s discretion. The 9 mg dose has been previously studied in postmenopausal women with metastatic breast cancer and was safe and well tolerated.

[000493] In TNBC patients, the 18 mg dose is preferred over a lower dose due to the aggressive phenotype of the disease and poor prognosis. Based on preclinical data, the 18 mg dose is more likely to saturate the AR and may lead to better clinical outcomes than a lower dose without receptor saturation or progesterone receptor inhibition. 18 mg dose may provide greater efficacy in TNBC without compromising subject safety.

[000494] Study design: This is an open label, multicenter, multinational, Phase 2 study to assess the efficacy and safety of Formula IX in female subjects with androgen receptor- positive, triple negative breast cancer (AR+ TNBC). Subjects will be administered Formula IX, 18 mg orally (PO) daily for up to 12 months. Simon’s two-stage (optimal) design will be used to assess primary efficacy and will require up to 41 evaluable subjects; i.e., subjects with centrally confirmed AR+ who receive at least one dose of study drug. In order to obtain these numbers of evaluable subjects, 21 to 55 subjects, including over-enrollees (see below), will be enrolled to receive a daily PO dose of Formula IX 18 mg. Fourteen of the aforementioned subjects may be over-enrollees to allow for replacement of subjects to account for lack of centrally confirmed AR+ status, or for the rare subject who is enrolled but does not receive study drug. The trial will test for an unacceptably low clinical benefit rate (CBR) of < 5% versus a CBR more consistent with > 20%. The first stage will be assessed among the first 21 evaluable subjects. If at least 2/21 subjects achieve clinical benefit (CB) (defined as complete response [CR], partial response [PR], or stable disease [SD], per Response Evaluation Criteria in Solid Tumors [RECIST], Version 1.12) at week 16, then the trial will proceed to the second stage of recruitment of up to a total of 41 subjects in the evaluable subset of the Full Analysis Set (FAS). Otherwise, the trial will be discontinued for lack of efficacy. [000495] Subjects who are not confirmed AR+ may remain on the trial, but will not be part of the primary efficacy analysis - these subjects will contribute to secondary and tertiary analyses. Subjects who experience an adverse event (AE) with Grade > 3 intensity (National Cancer Institute Common Terminology Criteria for Adverse Events [NCI-CTCAE], Version 4.0) and/or intolerance may have a dose reduction from 18 mg to 9 mg per day or a drug interruption based on the medical judgment of the Investigator and after confirmation by the study Medical Monitor. The subjects who demonstrate clinical benefit (CB) will be treated for up to 12 months from the date of the first dose of study treatment (as long as they continue to demonstrate CB from the treatment during these 12 months). Subjects who continue to demonstrate a beneficial response from the study treatment at 12 months will be offered to continue in a safety extension study under a separate protocol. All subjects will be folio wed- up for one month after the last dose of Formula IX is received, for safety purposes.

[000496] Primary efficacy objective of this trial is to estimate the clinical beneficial rate (CBR) at 16 weeks (defined as complete response (CR), partial response (PR), or stable disease (SD)) (by RECIST 1.1) of Formula IX 18 mg given orally (PO) daily in subjects with TNBC and centrally confirmed AR+ status.

[000497] Secondary efficacy objectives: Estimate the CBR at 16 weeks of Formula IX 18 mg in all subjects enrolled who receive at least one dose of study medication (i.e., the full analysis set (FAS)) regardless of AR status as determined by the central laboratory.

[000498] The following secondary efficacy objectives apply to both centrally confirmed AR+ subjects (the evaluable subset of the FAS) as well as to all subjects in the FAS:

• Estimate the objective response rate (ORR; defined as CR or PR) (by RECIST 1.1) of Formula IX 18 mg at 16 weeks.

• Estimate the CBR of Formula IX 18 mg at 24 weeks.

• Estimate the ORR (defined as CR or PR) of Formula IX 18 mg at 24 weeks.

• Estimate the best overall response rate (BOR) of Formula IX 18 mg.

• Estimate the progression free survival (PFS) of subjects receiving Formula IX 18 mg.

• Estimate the time-to-progression (TTP) of subjects receiving Formula IX 18 mg.

• Estimate duration of response (time from documentation of tumor response to disease progression or death) of subjects receiving Formula IX 18 mg. [000499] Tertiary objectives: The following tertiary efficacy objectives apply to both centrally confirmed AR+ subjects (the evaluable subset of the FAS) as well as to all subjects in the FAS :

• Assess the effect of Formula IX 18 mg on serum prostate specific antigen (PSA).

• Assess the effect of Formula IX 18 mg on Quality of Life (QoL) as measured by EQ- 5D-5L.

• Assess the effect of Formula IX 18 mg on circulating tumor cells (CTCs).

• Assess the impact of duration of prior CB on outcome.

• Assess the impact of time from diagnosis of metastases to study enrollment on outcome.

• Describe the effect of Formula IX 18 mg on tumor volumetries.

• Assess the effect of plasma concentrations of Formula IX and Formula IX glucuronide on CBR at 16 and 24 weeks.

[000500] Safety objective: To describe the safety profile of Formula IX 18 mg PO daily in subjects with TNBC and centrally confirmed AR+ as well as in all subjects enrolled and treated.

[000501] Pharmacokinetic objective: To describe the plasma concentrations of Formula IX and Formula IX glucuronide at each of the assessed time points.

[000502] Target population: Adult women with advanced TNBC with centrally confirmed AR+.

[000503] Subject Inclusion Criteria: Subjects eligible for inclusion in this study must meet all of the following criteria:

• Able and willing to give voluntary, written and signed, informed consent;

• Women > 18 years of age;

• Women with TNBC who have received at least one but no more than two prior chemotherapy regimens for the treatment of advanced or metastatic TNBC;

• Confirmation of AR+ (defined as > 10% nuclear AR staining by immunohistochemistry [IHC]) TNBC in either the primary or metastatic lesion, assessed during the screening period by a local laboratory or by medical history;

• TNBC confirmed by medical history as: human epidermal growth factor receptor 2 [HER2] -negative (confirmed by IHC 0, 1+ regardless of fluorescence in situ hybridization [FISH] ratio; IHC 2+ with FISH ratio lower than 2.0 or HER2 gene copy less than 6.0; FISH ratio of 0, indicating gene deletion, when positive and negative in situ hybridization [ISH] controls are present); estrogen receptor (ER) negative (confirmed as ER expression less than or equal to 1% positive tumor nuclei); progesterone receptor-negative (confirmed as progesterone receptor expression less than or equal to 1% positive tumor nuclei);

• Availability of paraffin embedded or formalin fixed tumor tissue; OR, a minimum of 10 and up to 20 slides of archived tumor tissue for central laboratory confirmation of AR status and molecular subtyping. Metastatic tumor tissue is preferred when possible;

• Subjects must have either measurable disease or bone-only non-measurable disease, evaluable according to RECIST 1.1;

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at the time of screening and enrollment;

• Negative pregnancy test in women of childbearing potential (premenopausal or less than 12 months of amenorrhea post-menopause, and who have not undergone surgical sterilization), no more than 7 days before the first dose of study treatment;

• For women of childbearing potential who are sexually active, agreement to use a highly effective, non-hormonal form of contraception during and for at least 6 months after completion of study treatment; OR, a fertile male partner willing and able to use effective non-hormonal means of contraception (barrier method of contraception in conjunction with spermicidal jelly, or surgical sterilization) during and for at least 6 months after completion of study treatment;

• Adequate organ function as shown by: Absolute neutrophil count > 1,500 cells/mm ³ ; Platelet count > 100,000 cells/mm3; Hemoglobin > 9 g/dL; Seram aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 2.5 Upper Limit of the Normal range (ULN) (or < 5 if hepatic metastases are present); Total serum bilirubin < 2.0 x ULN (unless the subject has documented Gilbert Syndrome); Alkaline phosphatase levels < 2.5 x ULN (< 5 x ULN in subjects with liver metastasis); Seram creatinine < 2.0 mg/dL or 177 μmol/L; International normalized ratio (INR) or activated partial thromboplastin time (aPTT) < 1.5 x ULN (unless on anticoagulant treatment at screening);

• Able to swallow capsules; • Any toxicity from prior chemotherapy has resolved orGrade 1 (NCI-CTCAE, Version 4.0).

Formulation, Packaging, and Labelling

[000504] Formula IX 3.0 mg Softgels will be supplied as opaque, white to off-white, size 5, oval Softgels. The liquid Softgel fill is composed of Formula IX dissolved in polyethylene glycol 400. Dosing instructions will be provided on the study drug label and in the subject information sheet.

EXAMPLE 27

FORMULA IX REDUCED THE GROWTH OF HER2-POSITIVE TUMORS Methods

[000505] HCI-007 tumor pieces (1 mm ³ ) were implanted surgically (one per mouse) under the skin on the flanks of NSG mice. Simultaneously, 17β-estradiol pellet (Innovative Research of America) was implanted surgically under the skin of each mouse. Tumors were allowed to grow and reach approximately 100 mm ³ volume (1*W*W*0.526). Mice were randomized and treated orally with vehicle (15% DMSO+85%PEG-300), Formula IX (10 mg/kg), or enzalutamide (20 mg/kg). Tumor volume was measured weekly and represented as % change in tumor volume (Figure 32). Mice were sacrificed and tumors stored for further analysis. Results

[000506] As described in Figure 32, ER-positive, PR-positive, HER2-positive and AR- positive tumors of animals treated with vehicle and enzalutamide grew comparably, while the tumors of mice treated with Formula IX grew slowly. Tumors of animals treated with Formula IX regressed during the first 7 days, before started to slowly increase. (See also Example 29, and Figures 35A-35C.)

Conclusion

[000507] These results support the previous results observed in MCF-7 cells xenograft demonstrating that Formula IX reduced the growth of HER2 -positive tumors. (See Example 29.)

EXAMPLE 28

FORMULA IX INHIBITS GROWTH IN HCI-013 PATIENT DERIVED XENOGRAFTS THAT ARE TRIPLE POSITIVE (ER, PR, HER2), AND ALSO

EXPRESS AR Methods

[000508] HCI-013 tumor pieces (1 mm ³ ) were implanted surgically (one per mouse) under the skin on the flanks of NSG mice. Tumors were allowed to grow and reach approximately 100 mm ³ volume (1*W*W*0.526). Mice were randomized and treated orally with vehicle (15% DMSO + 85% PEG-300) or Formula IX (10 mg/kg). Tumor volume was measured weekly and represented as % change in tumor volume. Mice were sacrificed, tumors weighed, and stored for further analysis.

Results

[000509] As described in Figures 33A and 33B, triple positive HER2 tumors of animals treated with vehicle grew robustly, while the tumors of mice treated with Formula IX grew very slowly. Tumors of Formula IX treated animals did not grow appreciably through the duration of the experiment suggesting that there is almost a 100% tumor growth inhibition (TGI) (Figure 33A). The tumor volume results are reflected in tumor weights observed at the end of the experiment (Figure 33B).

Conclusion

[000510] These results indicate that Formula IX is extremely potent in tumors that are triple positive (express ER, PR, and HER2) and also express AR. See also Example 29, where HCI- 13 was further characterized to include genotyping of the ER in the tumor which revealed the Y537S mutant ER was present in the HCI-13 tumor.

EXAMPLE 29

INHIBITION OF PROLIFERATION AND GROWTH OF PATIENT-DERIVED XENOGRAFTS (PDX) AND TISSUES THAT EXPRESS WILDTYPE AND MUTANT

REFRACTORY ER

[000511] In the study, it was found that proliferation and growth of patient-derived xenografts (PDX) and tissues that express wildtype and mutant refractory ER were inhibited by AR agonists and tissue-selective AR modulators (SARMs), but not by antagonists. The AR agonists inhibited the growth of these tumors by reprogramming the ER cistrome and subsequently inhibiting ER function and by altering the phosphokinome signature.

Materials and Methods

Reagents

[000512] TaqMan PCR primers and fluorescent probes, master mixes, and Cells-to-Ct reagents were obtained from Life Technologies (Carlsbad, CA). Cell culture medium and charcoal-stripped fetal bovine serum (csFBS) were purchased from Fisher Scientific (Waltham, MA). FBS was purchased from Hyclone (San Angelo, TX). AR-N20 antibody was procured from Santa Cruz Biotechnology (Santa Cruz, CA). Enzalutamide was purchased from MedKoo Biosciences (Chapel Hill, NC). ER-a (D8H8) antibody was procured from Cell Signaling (Danvers, MA). Actin antibody, DHT, tamoxifen, and fulvestrant were purchased from Sigma (St. Louis, MO). Vetspon dental cubes/sponges (Patterson Veterinary Supplies Inc., NC0654350) were obtained from Fisher Scientific (Waltham, MA). Epidermal growth factor (EGF) was purchased from R&D systems (Minneapolis, MN), phorbol 12-myristate 13- acetate (PMA) was obtained from Acros organics, and 17 β-eslradiol was obtained from Tocris (Bristol, UK). All other reagents used were analytical grade.

Cell culture

[000513] MCF-7 and ZR-75-1 cells were obtained from American Type Culture Collection (ATCC, Manassas, VA). The cells were cultured in accordance with the ATCC recommendations .

Growth assay

[000514] Cells were plated at varying densities in growth medium in 96 well plates. Cells were treated as indicated in the figures and viability measured using sulforhodamine B (SRB) or the number of cells counted using Coulter counter.

Transfection

[000515] MCF-7 stable cells were generated by lentiviral infection of green-fluorescent protein (GFP) or the AR cloned into pLenti U6 Pgk-puro vector as described earlier (Narayanan et al. (2014) PLoS One 9, el03202; Yang et al. (2010) Cane Res 70, 8108-8116; Yepuru et al. (2013) Clin Cancer Res 19(20), 5613-5625).

Tumor xenograft experiments

[000516] All animal protocols were approved by The University of Tennessee Health Science Center (UTHSC) Institutional Animal Care and Use Research Committee. Xenograft experiments were performed as previously published (Narayanan et al. (2014) PLoS One 9, el03202). Briefly, 3 million MCF-7 cells were suspended in 0.05 ml MEM+10% FBS and 0.05 ml Matrigel/nude mouse and were injected subcutaneously. Once the tumor size reached 100-200 mm ³ , the animals were randomized and treated orally with the indicated drugs formulated in DMSO:PEG-3CX) (15:85). HCI-7, HCI-9, and HCI-13 PDXs were gifts kindly donated by Dr. Alana Welm (Huntsman Cancer Institute, Salt Lake City, Utah). HCI PDX tumor fragments (1 mm ³ ) were surgically implanted under the mammary fat pad in female NOD SCID Gamma (NSG) mice. Tumor volume was measured twice weekly for MCF-7 xenograft and once or twice weekly for HCI PDXs. At the end of the study, animals were sacrificed and tumors were excised, weighed, and stored for various analyses.

Patient specimen collection

[000517] Specimens from breast cancer patients were collected with patient consent under a protocol approved by the UTHSC Institutional Review Board (IRB). Specimens were collected immediately after surgery in RPMI medium containing penicillin: streptomycin and Fungizone and transported to the laboratory on ice. The tissues were finely minced and treated with collagenase for 2 hours. The digested tissues were washed with serum-free medium and frozen in liquid nitrogen in freezing medium (5% D MS 0+95% FBS) or implanted under the mammary fat pad in female NSG mice.

Sponge culture

[000518] HCI-13 tumors grown in female mice were allowed to reach 500-1000 mm ³ before the animals were sacrificed and the tumors were excised to be used for sponge culture. Patient specimens frozen in liquid nitrogen in freezing medium were used for sponge culture. Sponge cultures were performed in accordance to the protocol published earlier (Dean et al. (2012) Cell Cycle 11, 2756-2761; Hu et al. (2016) Cancer Res 76, 5881-5893; Ochnik et al. (2014) Menopause 21, 79-88). Tumors were sliced into small pieces (~1 mm ³ ) and incubated on pre- soaked gelatin sponges (5 fragments/sponge) in 12 well plates containing 1.5 mL medium (MEM + 10% FBS + 2 mM L-glutamine + 10 μg/mL insulin + 10 pg/mL hydrocortisone + penicillin: streptomycin). The cultures were performed in triplicates for HCI-13 and singly for patient specimens. Pooled samples (n=5/sponge) from each sponge constituted one sample. Medium was replaced the next day and treated as indicated in the figures. Tissues were harvested after 3 days of treatment, RNA extracted, and expression of various genes measured. Although the same procedure was adopted for specimens obtained from breast cancer patients, the specimens were cultured singly (n=5/sponge=one sample) and not in triplicates as performed for HCI-13. Characteristics of the patient specimens used in PDX and in sponge cultures are provided in Table 12.

Table 12

Microarray

[000519] RNA from tumors was extracted and verified qualitatively and quantitatively. Total RNA (200 ng/sample; n=4/group) from each sample was amplified and labeled using the WT Plus Kit from Affymetrix and processed according to Affymetrix protocol. The arrays (Human ST2.0, Affymetrix, Santa Clara, CA) were washed and stained on Affymetrix Fluidics station 450 and scanned on an Affymetrix GCS 3000 scanner.

[000520] Data from microarrays were normalized using Affymetrix Expression Console. Mean, Standard Deviation, and Variance were calculated across the groups. Fold Change from vehicle-treated samples was calculated, and a fold change of 1.5 was used as cutoff. Student's t-test was used to determine the significance and a cutoff of p value < 0.05 was used for significance discovery. False discovery rate was calculated using Benjamini & Hochberg method, and a cutoff for FDR < 0.05 was used to create a significant differential expression list. The gene candidate list was loaded to Ingenuity Pathway Analysis and gene set enrichment analysis (GSEA) performed for further discovery. Microarray experiments were performed at the UTHSC Molecular Resources Center (MRC), and data analysis was performed by the UTHSC Molecular Bioinformatics (mBio) core facility.

Phospho-proteomics

[000521] Frozen samples from HCI-13 PDX treated with vehicle or Formula IX were cut into 8 pm cryosections and mounted on uncharged glass slides. Whole tissue lysates were directly prepared from the tissue sections using a 1:1 mixture of T-PER (Tissue Protein Extraction Reagent; Pierce, Rockford, IL) and 2X Tris-Glycine SDS Sample Buffer (Invitrogen, Carlsbad, CA) supplemented with 5% 2-mercaptoethanol. Samples were boiled for 8 minutes and stored at -80°C until arrayed.

[000522] Samples and standard curves for internal quality assurance were printed onto nitrocellulose-coated slides (Grace Bio-labs, Bend, OR) using an Aushon 2470 arrayer (Aushon BioSystems, Billerica, MA). Selected arrays were used to estimate the amount of protein in each sample using a Sypro Ruby Protein Blot Stain (Molecular Probes, Eugene, OR) protocol following manufacturer’s instructions (Pin et al. (2014) Curr Protoc Prtein Sci 75, Unit 2727). Remaining arrays were tested with a single primary antibody using an automated system (Dako Cytomation, Carpinteria, CA) as previously described (Baldelli et al. (2015) Oncotarget 6, 32368-32379). Arrays were first incubated with Reblot Antibody stripping solution (Chemicon, Temecula, CA), followed by two washes in PBS, and I-block solution (Tropix, Bedford, MA) for 4 hours. Arrays were probed with a total of 174 antibodies targeting a wide range of protein kinases and their activation via phosphorylation. Antibodies specificity was tested using standard immunoblotting on a panel of cell lysates. Selected arrays were stained with an anti-rabbit or anti-mouse biotinylated secondary antibody alone (Vector Laboratories Inc., Burlingame, CA and Dako Cytomation, Carpinteria, CA, respectively) and used as negative controls for nonspecific binding/background subtraction.

[000523] The commercially available Signal Amplification System (CSA; Dako Cytomation) and a streptavidin-conjugated IRDye 680 secondary antibody (LI-COR Biosciences, Lincoln, NE) were used as signal detection methods. Images were acquired on the laser-based PowerScanner (TECAN, Monnedorf, Switzerland), and data were analyzed using the MicroVigene software Version 5.1 (Vigene Tech, Carlisle, MA) as previously described (Baldelli et al. (2015) Oncotarget 6, 32368-32379). Intra and inter-assay reproducibilities have been previously reported (Pierobon et al. (2014) J Proteome Res 13, 2846-2855; Rapkiewicz et al. (2007) Cancer 111, 173-184).

Chromatin immunoprecipitation assay (ChIP) -Sequencing (ChIP-Seq) [000524] HCI-13 xenograft specimens were snap frozen and stored for ChIP-sequencing analysis. ChIP-Seq study was performed in vehicle or Formula IX -treated HCI-13 PDX grown in NSG mice. ChIP was performed with ER (n=4/group) or AR (n=/group) antibodies and genome-wide sequencing was performed on a NextSeq 500 sequencer. For ChIP, a standard SDS-based protocol was used, as has been described (Carroll et al. (2005) Cell 122, 33-43). Briefly, a whole cell lysate was made from tissues. The lysate was sonicated using a Covaris E210 machine (Covaris Inc., Wobum, MA), for 30 min per sample (settings: duty cycle 20%, intensity 8 at 200 cycles per burst). ER or AR was immunoprecipitated, washed, and the complex eluted. The DNA-protein complex was reverse cross-linked by incubating at 65 °C for 6 hours to overnight. After reverse cross-linking, precipitated and input DNA was purified using QIAquick PCR purification columns (Qiagen).

[000525] For library preparation the ThruPLEX-FD Prep Kit (Rubicon Genomics, Ann Arbor, MI) was used. For each library 2-10 ng DNA was used. After amplification, fragments of 200-600 bp were selected using a Pippin Prep machine using 2% agarose ethidium bromide- containing cassettes (Sage Science, Beverly, MA). After size selection, the DNA was cleaned using Ampure beads and analyzed on a Fragment Analyzer (Advanced Analytical, Ames, IA). For sequencing, NextSeq 500 sequencing platform (Illumina, San Diego, CA) was used. Human genome build 19 (hgl9) was used as the reference genome. Sequencing data from ChIP experiments were aligned to the human genome using Bowtie. For peak calling MACS2 was used.

Immunohistochemistry

[000526] Fourteen cases of invasive breast cancer, luminal B subtype, were chosen randomly from the formalin fixed paraffin embedded samples available from the tissue bank of the pathological department of Tohoku University Hospital. The luminal B classification of these samples was on the basis of having ERa expression greater than 1% and a Ki-67 labelling index of greater than 20 percent. The samples had variable levels of PR expression (Labelling Index, Average 48.9, Range 0-100) and other clinicopathological characteristics (Ki67, Average 38%, Range 20-48%; Nottingham Grade, 1 n=l, 2 n=10, 3 n=3). The use of these samples was approved by the Tohoku University School of Graduate Medicine Ethic review board (2014-1-107). Blocks of tissue were retrieved and sectioned at a thickness of 3 mM and mounted on glass slides. In order to assess co-localisation mirror image sectioning was used. The slides were then stained for ERa and AR (ERa, 1:50 dilution, Clone 6F11, Leica; AR, 1:50 dilution, Clone AR441, Dako) using immunohistochemistry as previously described (McNamara et al. (2013) Cancer Sci 104, 639-646; Niikawa et al. (2008) Clin Cancer Res 14, 4417-4426).

Statistics

[000527] Statistical analysis was performed using GraphPad prism software (La Jolla, CA). Experiments containing two groups were analyzed by simple t-test, while those containing more than two groups were analyzed by one way analysis of variance (ANOVA) followed by Tukey post-hoc test. Microarray, phospho-proteomics, and ChIP-Seq statistical analyses are described under the respective methods.

[000528] All in vitro experiments were performed at least in triplicate. Data are represented as mean ± S.E.

Results

[000529] The SARM Formula IX, is an AR agonist that binds to and activates the AR at less than 10 nM (Narayanan et al. (2014) PLoS One 9, el03202; Ponnusamy et al. (2017) Hum Mol Genet. 26(13), 2526-2540). Clinically, Formula IX has been evaluated in over 1000 patients in multiple clinical trials (see Example 26 for a partial list) and was shown to increase lean mass and physical function without having significant virilizing side effects (Dobs et al. (2013) Lancet Oncol 14, 335-345). One of the motivating factors to explore SARMs in preclinical studies for breast cancer was that SARMs are non-metabolizable SARMs to weaker androgen or estrogen metabolites which confound results in breast cancer, which is in contrast with steroidal androgens such as DHT.

Formula IX inhibited (ER, PR, and AR positive) breast cancer cell proliferation

[000530] To determine the effect of AR agonists on the proliferation of ER-positive breast cancer cells, ZR-75-1 breast cancer cells that endogenously express AR, ER, and PR were treated with vehicle or a dose response regimen of Formula IX and the number of cells were counted after 6 days of treatment. Proliferation of ZR-75-1 cells was significantly reduced dose dependently by Formula IX (Figure 34A). The results were reproduced in MCF-7 cells stably transfected with AR, but not with GFP (Figure 34B). Although a few previous reports have shown that MCF-7 cells express AR and respond to AR ligands (Buchanan et al. (2005) Cancer Res 65, 8487-8496), the MCF-7 cell line clone in the study lacks or minimally expresses AR, which is in concordance with other reports (De Amicis et al. (2010) Breast Cancer Res Treat 121, 1-11). [000531] Tumor microenvironment contains tumor epithelial cells, stromal cells, cancer- associated fibroblasts (CAFs), and endothelial cells. The collective function of these cells promotes the aggressive growth of tumors due to secretion of paracrine factors. The CAFs are important for the sustained growth of cancers, and they differ from normal fibroblasts in their capacity to secrete factors that promote proliferation of cancer cells. To determine how an AR agonist affects the paracrine factors secreted by CAFs and subsequently the proliferation of epithelial cells, CAFs were isolated from an ER, PR, and AR-positive breast cancer tissue obtained from a 59-year-old African American patient (Sample ID 1005). The CAFs were treated with vehicle, 10 nM DHT, or 1 mM Formula IX or 1 mM of an AR antagonist, enzalutamide. Medium was collected over a period of 10 days and pooled. CAFs were stained with SRB to evaluate the effect of AR ligands on proliferation. Of the tested materials, neither AR agonist, DHT and Formula IX, nor AR antagonist enzalutamide, affected the proliferation of breast cancer CAFs (Figure 34C, left side).

[000532] MCF-7 cells stably transfected with GFP (MCF-7-GFP) that lack AR were plated in 96 well plates and fed with conditioned medium obtained from CAFs treated with vehicle, DHT, Formula IX, or enzalutamide· Conditioned medium was replaced on days 4 and 7 and the cells were stained with SRB to measure viability. Both DHT and Formula IX -treated conditioned medium, but not en zal utam i de- treated medium, inhibited the proliferation of MCF-7-GFP cells (Figure 34C, right side). The anti-proliferative effects rendered by DHT and Formula IX would have evolved from inhibiting any paracrine secretion that occurred in CAFs, and could not be direct effects on the AR-negative MCF-7 clone.

Formula IX inhibited wild-type ER-positive breast cancer PDX (HCI-7) growth

[000533] To determine if the growth inhibitory properties of Formula IX in vitro could be observed in vivo, Formula IX was tested in a PDX expressing wildtype AR. From the several PDXs available, three AR-positive PDXs were identified, based on gene expression profile. These PDXs, HCI-7, HCI-9, and HCI-13 (Table 12) express high levels of AR that are comparable to the expression found in LNCaP cells (Figure 35A). To determine the effect of Formula IX on the growth of wildtype ER-positive breast cancer PDX, HCI-7 (wtER-positive, PR-positive, AR-positive) luminal A tumor fragments were implanted under the mammary fat pad of female NSG mice. Once the tumors reached 100-200 mm ³ , the mice were randomized and treated orally with vehicle, 10 mg/kg Formula IX, or 30 mg/kg enzalutamide. The enzalutamide dose was selected based on previous published experiments (Park et al. (2016) Cancer Invest 34, 517-520; Pollock et al. (2016) Nat Chem Biol 12, 795-801) as well as from internal experiments conducted in prostate cancer xenografts and in Hershberger studies. The growth of HCI-7, which is a slow growing tumor, was inhibited significantly by Formula IX, but not by enzalutamide (Figure 35B (see also Figure 32)). Tumor weights measured at the end of the study were also significantly smaller in the Formula IX -treated group (Figure 35C).

[000534] To confirm the results obtained in HCI-7, a xenograft was developed with MCF-7 cells (wtER, PR and HER2 positive) stably transfected with AR (MCF-7-AR) that express wildtype ER. Tumor volumes, measured three times per week, were significantly reduced by Formula IX with a calculated tumor growth inhibition of greater than 60% (Figure 35D), supporting the use of SARMs in ER-positive and AR-positive breast cancers.

[000535] To determine if the same effect is observed in an AR-positive, but ER-negative breast cancer, HCI-9 tumor fragments were implanted under the mammary fat pad of NSG mice. Once the tumors grew to 100-200 mm ³ , the animals were randomized and treated orally with vehicle, Formula IX, or enzalutamide· Neither Formula IX nor enzalutamide altered the growth trajectory of the tumors, indicating that the AR agonist was not effective in HCI-9 PDX that does not express ER (Figure 34D). Collectively, these results indicate that the AR might require ER to inhibit cell proliferation and tumor growth.

AR agonist inhibited growth of estrogen-independent mutant ER-positive PDX (HCI-13)

[000536] It was discovered by internal sequencing as well as from literature that HCI-13 PDX expresses an ER that is mutated in the LBD at Y537 (Sikora et al. (2014) Cancer Res 74, 1463-1474). This mutation frequently occurs in refractory ER-positive breast cancers that have been treated with ER antagonists (e.g., tamoxifen or fulvestrant) or aromatase inhibitors (e.g., letrozole, anastrozole, exemestane) (Jeselsohn et al. (2018) Cancer Cell 33, 173-186; Toy et al. (2017) Cancer Disc 7, 277-287) . Genome- wide ChIP-seq studies with cells expressing this mutant indicated that the DNA binding signature of this mutant ER is distinct from that of the wildtype ER and that this mutation reprogrammed the ER cistrome. HCI-13 was obtained from a patient who was treated with and relapsed from drugs ranging from ER-targeted therapeutics to chemotherapy (Table 12). To determine whether this ER mutant expressing PDX is dependent on estrogen for growth, HCI-13 tumors were implanted under the mammary fat pad in sham-operated and ovariectomized mice. Tumor growth was monitored over a period of 4 weeks. The growth rate in both sham-operated and in ovariectomized mice was comparable, indicating that the ER in HCI-13 is constitutively active and does not require estrogen to grow (Figure 36A).

[000537] To determine if Formula IX will have the ability to inhibit the growth of a constitutively active mutant ER-driven breast cancer, HCI-13 tumor fragments were implanted under the mammary fat pad in NSG mice. Once the tumors attained 100-200 mm ³ , the animals were randomized and treated with vehicle or Formula IX. Formula IX inhibited the growth of HCI-13 by almost 95% (Figure 36B and Figure 36C). The tumors that were weighed at the time of sacrifice also reflected an almost complete inhibition of tumor (Figure 36C).

[000538] Since the Y537S mutation in the ER-FBD results in resistance of ER antagonists, degraders, and aromatase inhibitors, it was hypothesized that the mutant ER in HCI-13 might be refractory to the inhibitory effects of ER antagonists. To prove this hypothesis, ex vivo sponge culture was used to grow HCI-13. HCI-13 tumor fragments were cultured on gelatin sponges as described in the methods and were treated with vehicle, DHT, Formula IX, enzalutamide, and fulvestrant. At the end of 3 days of incubation, the tumors were harvested, RNA isolated, and the expression of ER- and AR-target genes was measured by real time PCR (Figure 36D-Figure 36G).

[000539] The results clearly show that while fulvestrant, a clinically used effective ER degrader, was ineffective, DHT and Formula IX were effective in inhibiting the expression of constitutively active ER-induced pS2 and PR gene (Figure 36D-Figure 36E). Both DHT and Formula IX induced the AR-target gene, FKBP5 (Figure 36F), indicating that the AR is functional. Measurement of the proliferation marker MKI67 (i.e., Ki67) indicated that similar to the expression of pS2 and PR, MKI67 expression was inhibited by Formula IX and DHT, but not by fulvestrant or enzalutamide (Figure 36G). These results were reproduced in an ER transactivation assay with an ER cDNA cloned from HCI-13 (Figure 34E). While fulvestrant and tamoxifen inhibited the activity of wildtype ER (Figure 34E , left side), HCI-13 ER was not inhibited by either of the compounds (Figure 34E, right side). These results confirm that when ER inhibitors and degraders develop resistance, AR agonists might offer a mechanistically distinct approach to inhibit the resistant ER function.

Ex vivo culture with ER-positive (except 2005 and HCI-9) tumor specimens indicated the heterogeneity of response to ER and AR ligands [000540] Like other cancers, breast cancer is also heterogeneous in its genomic profile as well as in its response to treatments. To determine the effect of Formula IX and fulvestrant on growth inhibition, breast cancer specimens obtained from patients were cultured, on dental sponges, as indicated above. The specimens were treated with vehicle, 1 mM Formula IX, or 100 nM fulvestrant. Three days after treatment, RNA was isolated from the tissues and expression of ER- and AR-target genes was measured. Expression of the AR and ER plotted as relative to HCI-13 expression indicates that the two targets were expressed only at a fraction of the levels observed in HCI-13 (Figure 36K). HCI-13 expresses AR at levels comparable to that of LNCaP prostate cancer cells and the other specimens ranged from 0.2-20%, with the triple- negative specimen, 2005, having the least expression. Fulvestrant inhibited the ER function in 4 of 8 specimens, while Formula IX inhibited the ER function in 3 of 8 specimens (Figure 36H-Figure 361). Interestingly, Formula IX inhibited the ER function in specimen 1005, where fulvestrant functioned as an agonist. Specimen 1005 could be comparable to that of HCI-13 in its response to ER antagonists. These results are in concordance with the HCI-13 observation that AR agonists might inhibit ER function even in cases where ER antagonists will fail to inhibit. The ability of Formula IX to be an AR agonist was observed in 4 of 8 specimens (Figure 36J) which included all 3 specimens for which Formula IX was able to suppress ER function. Moreover, as most of these patients have not received many treatments prior to the procurement of the tissues (Table 12), nomutation in the ER was expected.

Formula IX inhibited HCI-13 breast cancer growth by inhibiting the function of constitutively active ER

[000541] The gene expression studies in sponge culture demonstrate that the AR agonists inhibit ER- target genes. To determine the mechanism for the anti-proliferative effects of Formula IX in HCI-13, RNA from HCI-13 tumors obtained from animals shown in Figure 36B-Figure 36C were subjected to Affymetrix microarray. In total, 3029 genes were differentially regulated by Formula IX in HCI-13 tumors compared to vehicle-treated tumors. Formula IX up-regulated 1792 genes and down-regulated 1237 genes. Heatmap of the differentially regulated genes clearly indicates a shift in the expression pattern of genes due to Formula IX treatment (Figure 37A). Some of the most up-regulated genes include Cyp4F8, MYBPC1, RAB3B, LRRC26, AQP4, and CST4 (Figure 37B). Although the role of upregulated genes like Cyp4F8 and Mybpcl in breast cancer is unclear and needs to be determined, downregulated genes such as MUC-2 and IL1 ORA ) have been shown to play important role in cancers.

[000542] Ingenuity pathway analysis (IP A) showed that the ER-target genes were highly enriched even more than the AR-target genes in Formula IX -treated specimens (p values of 6.66 ¹¹ vs 2.83 ⁷ ; Figure 37C). A subset of the ER-target genes was down-regulated by Formula IX, while all the AR-target genes were up-regulated by Formula IX (Figure 37D-Figure 37G). While ER-target genes such as TFF1, PGR, NRIP1 were down-regulated by Formula IX (not shown), other ER-target genes such as CTSD and CCND1 were not inhibited by Formula IX. These results provide evidence that Formula IX functions in breast cancer by at least partially inhibiting the ER- signaling pathway to reduce the growth of cancer.

[000543] Some direct and indirect regulation of ER-targets were observed in Formula IX - treated samples. ER increases PDZK1 expression, which in-turn inhibits the expression of SLC26A3, a tumor suppressor gene . Interestingly, Formula IX significantly inhibited the expression of PDZK1, which restored the expression of the tumor-suppressor gene, SLC26A3. Similarly, anti-apoptotic gene BCL-2 and genes present in its network such as PARP and WT1 were significantly down-regulated by Formula IX. Although these genes do not belong to the list of ER-direct target genes, cross-talk between ER and the BCF-2 pathway has been reported previously. Expression of another class of oncogenic proteins, histone class , was inhibited by Formula IX. About 17 members of histone group were inhibited significantly by Formula IX. The histone class has been implicated in aggressive cancers and endocrine-resistance (Nayak et al. (2015) Horm Cancer 6, 214-224).

[000544] Although IPA analysis did not provide any evidence for regulation of ERBB2 (human epidermal growth factor receptor 2 or HER2/neu) pathway by Formula IX, GSEA enrichment analysis revealed that Formula IX affected the genes regulated by ERBB2 (Figure 37H). It is not clear at this point whether the regulation of ERBB2 is a result of growth inhibition or inhibition of the ER pathway. Irrespective of the mechanism, a downregulation of ERBB2 pathway, which is an oncogenic and tumor-promoting pathway, may be an added advantage of using Formula IX or an AR agonist in ER-positive breast cancers.

ChIP-Seq analysis demonstrates that Formula IX reprogrammed ER and AR cistromes

[000545] Previous studies have demonstrated that the interaction of Y537S mutant ERwith DNA has been reprogrammed and might share limited similarity to the wildtype ER genome interaction. To determine if the effect of Formula IX on ER function is due to direct effect on ER binding to DNA, ChIP-sequencing was performed in the tumor samples obtained from animals shown in Figure 36B-Figure 36C. ER binding to 1248 regions (q<0.05) on the DNA was reprogrammed by Formula IX, with 792 regions enriched with ER and 456 regions depleted of ER (Figure 38A and Figure 38H). AR showed a similar pattern of DNA binding i.e. regions enriched with ER were also enriched for AR, and the regions that were depleted of ER were also depleted of AR (Figure 38A and Figure 38H). This indicates that the ER and AR are potentially shuttling as a complex. The motifs that were enriched by the ER represent androgen response element (ARE; SEQ ID NO: 1), glucocorticoid response element (GRE; SEQ ID NO: 2), and Forkhead box protein A1 or FOXA1 response elements (FOXA1RE; SEQ ID NO: 3), while the regions that were depleted of ER represent estrogen response element (ERE; SEQ ID NO: 4) and FOXA1RE (SEQ ID NO: 5) (Figure 38A and Figure 38H). Although the regions depleted by ER favor the gene expression pattern, the enrichment of ER at AREs and GREs is surprising and has not been previously reported. The principal component analysis (PCA) plot suggests the clear demarcation in the clustering of vehicle- and Formula IX - treated samples (Figure 38C). Figure 38B and Figure 40 show representative regions enriched and depleted of ER and AR. AR and ER binding to pS2 ERE, PSA (KLK3) promoter ARE, and PSA enhancer ARE was validated by ChIP real-time PCR (Figure 38D). It is important to recognize that as Formula IX neither binds to ER nor alters ER activity (Kearbey et al. (2007) Pharmaceutical Res 24, 328-335; Narayanan et al. (2008) Molecular Endocrinology 22, 2448-2465) its effect on ER cistrome is mediated by activating the AR.

[000546] As this is the first study to evaluate the effect of AR agonists such as DHT and Formula IX on ER cistrome in ER-positive breast cancers, the regions bound by ER were mapped in response to Formula IX. Between 50 and 60% of the ER enriched and depleted sites were mapped to distal regulatory regions, while only around 2-3% of the sites mapped to promoter regions (Figure 38E). Interestingly, while the intron and exon binding percentage match with previous reports, the proportion of the ER bound to promoters and distal regulatory elements are distinct from that observed in response to estrogens or with a constitutively active ER . Other studies have indicated that the ER cistrome comprises of about 30-40% at distal regulatory regions and 7-22% in proximal promoter regions, and AR-regulated ER cistrome comprises of 50-60% and 2-3% of these regions, respectively.

Formula IX reprogrammed the FOXA1RE sites [000547] It is interesting to observe that FOXA1RE motifs are represented in both the enriched and depleted ER cistrome. The enriched cistrome motifs represent ARE, GRE, and FOXA1RE, while the depleted cistrome motifs represent ERE and FOXA1RE. As FOXA1 pioneering transcription factor is important for the function of both AR and ER and has overlapping binding sites with ARE and ERE, it is highly possible that the activated AR might sequester FOXA1 from the FOXAlREs adjacent to the EREs to open up the nucleosome and facilitate its binding to ARE and GRE. Since ER is functioning as a complex with AR, it is also sequestered from EREs and FOXAlREs towards AREs, GREs, and FOXAlREs. To determine the validity of this hypothesis the motifs shared by ERE and FOXAlREs were mapped in the downregulated cistrome. The majority of the EREs and FOXAlREs overlap in the downregulated motifs (Figure 38F). On the other hand, majority of the GREs and AREs in the upregulated motifs overlap with FOXAlREs. The results of this analysis confirm the hypothesis that the ER:AR:FOXAl complex shuttles from the ER binding sites to AR binding sites to facilitate the conversion of nucleosomes to open chromatin and AR binding.

[000548] To confirm that the AR and ER are localized as a complex and that they migrate together between cistromes, an immunoprecipitation was conducted with ER and AR antibodies and Western blot for SRC-1. It was hypothesized that if the AR and ER exist as distinct, separate complexes, Formula IX treatment will increase the interaction of SRC-1 with AR and reduce the interaction with ER. If AR and ER exist as a complex together, then Formula IX treatment will increase the interaction of both AR and ER with SRC-1. Treatment of HCI-13 PDX with Formula IX resulted in an increase in the interaction between AR and SRC-1 and also between ER and SRC-1 (Figure 38G). Although this is not a direct evidence for the AR:ER complex, this evidence combined with ChIP-Seq data suggest that the two proteins exist as a complex and the main difference is the cistrome binding that results in activation or inactivation of genes.

AR and ER colocalized in luminal B breast cancers

[000549] To determine the nuclear reactivity of AR and ER and potential colocalization in breast cancer specimens, immunohistochemistry was performed in several luminal B breast cancer specimens. Nuclear immunoreactivity of both AR and ER and expression at high levels was observed in all the breast cancer specimens examined (Figure 39). Additionally, several samples had moderate levels of cytoplasmic immunoreactivity for both markers. As levels of expression of both markers exceeded 60% in all samples, a high percentage of cells were positive for both ER and AR. The patterns of staining were also similar between the markers. Overall, the number of cells immunoreactive for AR in any one sample exceeded those which were immunoreactive for ER. However, the semi-quantitative nature of immunohistochemistry precludes us from being able to state conclusively that AR was expressed at greater levels than ERa. It was also possible to observe samples in which immunoreactivity for AR was weaker or absent while ER immunoreactivity was present; however, these were less frequent.

Phospho-proteomic analysis showed the inhibition of oncogenic and induction of tumor- suppressor protein phosphorylation by AR agonist

[000550] To determine the effect of Formula IX on the functions of various proteins, phospho-proteomics was performed in HCI-13 tumors treated with vehicle or Formula IX. Formula IX inhibited the phosphorylation of various oncogenic proteins such as pERK, PKC ¾ RSK3, Ezrin, BCL2, ELF4G, and ER (Figures 41A-Figure 41C). Formula IX also inhibited the expression of proliferation marker Ki67. Alternatively, Formula IX increased the phosphorylation of tumor suppressor proteins such as p53, p27, ACC, and the AR. Formula IX also increased the phosphorylation of STAT5, which could be a tumor suppressor or an oncogene depending on the context (Figures 41A-Figure 41C). These results demonstrate that activating the AR with an agonist promotes the alteration of appropriate pathways that facilitate tumor growth inhibition.

[000551] To understand the consequences of these protein alterations, cell signaling activators and inhibitors in HCI-13 sponge cultures were used to determine their effects on AR and ER target gene expression, FKBP5 and pS2, respectively. Because ERK and PKC phosphorylation were down-regulated by Formula IX, HCI-13 sponge cultures were treated with activators of the two pathways, EGF and PMA (Figure 41D-Figure 41E). Treatment of HCI-13 tumor fragments with PMA completely reversed the pS2 gene expression that was inhibited by Formula IX, while EGF only marginally reversed the inhibition observed with Formula IX. PMA reversed the effects of Formula IX on pS2 gene expression without affecting the ability of Formula IX to increase the expression of AR target gene, FKBP5 (Figure 41E). This suggests that PMA is potentially working downstream of the AR to regulate the ER.

Discussion [000552] Almost all oncology therapeutics are inhibitors or antagonists of their therapeutic targets. Prolonged use of these agents will result in selective pressure and eventually resistant mutations. These resistant mutations can either attenuate or prevent the anti-tumor activity of the drug or in the worst case scenario convert the drug into an agonist and cause aggressive tumor growth. In the presence of an agonist, the AR will exist in an agonistic conformation as observed in nature and not in an unstable antagonistic conformation. This conformational property might be less prone to the formation of AR mutations that could prevent AR binding or cause agonist effects on the cistrome.

[000553] The results obtained in HCI-13 are extremely encouraging. A tumor that relapsed and continued to grow in the presence of a range of therapeutics was inhibited by Formula IX (an AR agonist and nonsteroidal SARM) with a tumor growth inhibition of over 90%. This result and the result from ex vivo studies support the use of SARMs even after the tumors relapse from other treatment options. Although the HCI-13 is only one example of mutant ER, this mutation Y537S is one of the common mutants found in the clinic and could serve as a representative (Katzenellenbogen et al. (2018) Nat Rev Cancer 18(6), 377-388).

[000554] The unique property of inhibiting the ER function by activating the AR demonstrates the complex interaction between various nuclear receptors and their associated proteins. The microarray results indicate that the inhibition of ER and HER2 (human epidermal growth factor receptor 2) pathways by Formula IX could provide greater benefit to patients in whom both oncogenic pathways are activated. This beneficial effect is further enhanced by the increase in the phosphorylation of various tumor suppressors and inhibition of the phosphorylation of oncogenes.

[000555] The ChIP-Seq results suggest that the AR and ER exist as a complex in the presence of Formula IX and shift from an ER cistrome to an AR cistrome along with the pioneering transcription factor FOXA1. Based on these results, a model was proposed (Figure 42). In the absence of an activated AR, the constitutively active ER binds to EREs by utilizing FOXAlREs to create an open chromatin and promote the growth of the tumor. In the presence of an AR agonist, AR interacts with ER and the complex shifts from ERE and adjacent FOXAlREs to ARE and adjacent FOXAlREs. In this case, the FOXA1 is sequestered away from EREs towards AREs to open the nucleosomes and facilitate the binding of the complex.

[000556] Overall, these mechanism-based preclinical and translational studies support the use of an SARMs such as Formula IX to treat refractory hormone receptor-positive breast cancer. Further, heterogeneity is seen the response of ER-positive clinical specimens and hence it might be optimal to pharmacogenomically screen for Y537S ER mutant expressing breast cancers in order to enriched the clinical benefit rate of Formula IX. Tissue- selective AR agonism might offer an alternative hormonal approach for hormone receptor-positive breast cancers.

EXAMPLE 30

THE EFFICACY AND SAFETY OF FORMULA IX ON METASTATIC OR LOCALLY ADVANCED ER+/AR+ BREAST CANCER (BC) [000557] Study design: This was an open label, multicenter, multinational, randomized, parallel design Phase 2 study, and was to assess the efficacy and safety of Formula IX in postmenopausal subjects with ER+/AR+ BC. Subjects were randomized to receive either Formula IX 9 mg or 18 mg given PO daily for up to 24 months. Each dose arm was treated independently, and each assessed for efficacy using Simon’s two-stage (optimal) design (Simon R. Optimal two-stage designs for Phase 2 clinical trials. Controlled Clinical Trials 1989; 10: 1-10). Subjects were randomized in a 1:1 fashion to one of the two dose arms. [000558] Randomization was stratified by subjects presenting with bone only metastases and all other subjects, and further by setting of immediately preceding therapy (adjuvant setting or metastatic setting) in order to balance the proportion of subjects with these presenting features in each dose arm. There was no intent to statistically compare the two dose arms, but to determine whether either or both doses resulted in an acceptable clinical benefit response (CBR), defined as the proportion of evaluable subjects (i.e., subjects with centrally confirmed AR+ and who received at least one dose of study drug) with either CR, PR, or SD by RECIST 1.1 at week 24 while maintaining an acceptable safety profile. Given such a result, future exploration of Formula IX in ER+/AR+ BC would be warranted at that dose level.

[000559] Thirty-six to eighty-eight (36-88) subjects with centrally confirmed AR+ who received at least one dose of study drug (evaluable subjects) were needed for primary efficacy analysis purposes and were a subset of the full analysis set (FAS). Fifty patients in the 9 mg cohort and 52 patients in the 18 mg cohort met these criteria. One hundred seventy two (172) subjects, including replacement subjects, were randomized in a 1:1 fashion to receive a daily PO dose of either Formula IX 9 mg or 18 mg. Thirty of the aforementioned subjects were considered replacement subjects to account for lack of centrally confirmed AR+ status or for the rare subject that was randomized but did not receive study drug (assumes 25% of enrolled subjects were not evaluable for the primary efficacy analysis). Other statistical parameters that were part of the sample size calculation are a = 0.025 (one-sided) and power = 90%. The first stage in each study arm was assessed among the first 18 evaluable subjects. Greater than 3/18 subjects achieved CB (defined as CR, PR, or SD) at week 24, and both arms proceeded to the second stage of recruitment up to a total of 44 evaluable subjects per arm. Otherwise, the arm would have been discontinued for lack of efficacy. Statistical significance, i.e., rejection of the null hypothesis of an unacceptably low CBR of < 10% in favor of the alternative hypothesis that indicated the higher rate, > 30%, was more likely, would be declared if at least 9/44 subjects achieved CB at week 24 in that arm.

[000560] Subjects who were not centrally confirmed AR+ remained on the trial, but were not part of the primary efficacy analysis - these subjects contributed to secondary and tertiary analyses.

[000561] Subjects on the 18 mg treatment arm who experienced an adverse event (AE) with Grade > 3 intensity (National Cancer Institute-Common Terminology Criteria for Adverse Events [NCI-CTCAE], Version 4.0) and/or intolerance may have had a dose reduction from 18 mg to 9 mg per day or a drug interruption based on the medical judgment of the Investigator and after confirmation by the study Medical Monitor. The drug interruption may have lasted for a period of up to 5 days after which the subject must be rechallenged with study drug (18 mg or 9 mg) or discontinued from the study. In the case of a dose reduction, once the AE had resolved or reduced in intensity to Grade 1, the subject may have been rechallenged with 18 mg or maintained at 9 mg at the discretion of the Investigator.

[000562] Subjects on the 9 mg treatment arm who experienced an AE with Grade > 3 intensity (NCI-CTCAE 4.0) and/or intolerance may have had a drug interruption based on the medical judgment of the Investigator and after confirmation by the study Medical Monitor. The drug interruption may last for a period of up to 5 days after which the subject must be rechallenged with study drug (9 mg) or discontinued from the study.

[000563] For safety analysis, subjects were analyzed in the treatment arm in which they were initially dosed. For efficacy analysis, subjects were analyzed according to the treatment arm to which they were randomized.

[000564] The subjects who demonstrated CB were treated for up to 24 months from the date of randomization (as long as they continued to demonstrate CB from the treatment during these 24 months). Subjects who continued to demonstrate a CB from the study treatment at 24 months would have been offered to continue in a safety extension study under a separate protocol. For safety purposes, all subjects would have been followed-up for one month after the last dose of Formula IX was received.

[000565] For safety purposes, all subjects were followed-up for one month after the last dose of Formula IX was received.

[000566] Target Population: Adult postmenopausal women with metastatic or recurrent locally advanced ER+/AR+ BC.

[000567] Study Duration: The study duration was estimated at 3 years.

[000568] Description of Agent or Intervention: Three (3) Formula IX 3.0 mg softgels for a 9 mg daily dose or six (6) Formula IX 3.0 mg softgels for an 18 mg daily dose were taken PO with water at approximately the same time each day, with or without food.

[000569] Potential Benefits: Based on the trial of Example 9, Formula IX 9 mg once daily were studied in 22 postmenopausal women with metastatic ER+ BC who had previously responded to hormonal therapy. The primary endpoint was assessed in 17 AR-positive subjects. Six of these 17 subjects demonstrated CB (SD) at six months. In one subject with SD (RECIST 1.1), tumor regression of 27% in a single target lesion was demonstrated. Seven subjects in total (one subject with indeterminate AR status) achieved CB at six months. Among the seven subjects who achieved CB at six months, time to progression (TTP) was estimated as 10.2 months. The results also demonstrated that, after a median duration on study of 81 days, 41 percent of all subjects (9/22) achieved CB as best response and also had increased PSA, which appeared to be an indicator of AR activity. As of the finalization of this protocol, the study was still ongoing with one subject whose disease remained stable beyond 336 days. [000570] Preclinical data with Formula IX suggested that it was also anabolic in bone and decreases bone turn over markers. Treatment with Formula IX may decrease bone turn over as compared with other hormonal therapies for the treatment of hormone receptor positive BC. Stronger bone microenvironment may decrease metastases to bone or delay time to skeletal related events.

[000571] Efficacy Obj ectives

[000572] The primary efficacy objective of this trial was to estimate the CBR at 24 weeks (defined as complete response [CR] , partial response [PR] , or SD) (by RECIST 1.1) of Formula IX 9 mg and of Formula IX 18 mg given PO daily in subjects with estrogen receptor positive and androgen receptor positive (ER+/AR+) BC who had centrally confirmed AR+ status. [000573] The secondary efficacy objectives were to estimate the CBR at 24 weeks (by RECIST 1.1) of Formula IX 9 mg and 18 mg in all subjects randomized who received at least one dose of study medication (the full analysis set [FAS]) regardless of AR status as determined by the central laboratory.

[000574] The additional secondary efficacy objectives applied to both centrally confirmed AR+ subjects (the evaluable subset of the FAS) as well as to all subjects in the FAS: (a) Estimate the objective response rate (ORR; defined as CR or PR) (by RECIST 1.1) of Formula IX 9 mg and 18 mg at 24 weeks; (b) Estimate the best overall response rate (BOR) of Formula IX 9 mg and 18 mg; (c) Estimate the progression free survival (PFS) of subjects receiving Formula IX 9 mg and 18 mg; (d) Estimate the TTP of subjects receiving Formula IX 9 mg and 18 mg; and (e) Estimate duration of response (time from documentation of tumor response to disease progression or death) of subjects receiving Formula IX 9 mg and 18 mg.

[000575] The tertiary objective applied to both centrally confirmed AR+ subjects (the evaluable subset of the FAS) as well as to all subjects in the FAS (a) Assess the effect of Formula IX 9 mg and 18 mg on serum PSA; (b) Assess the effect of Formula IX 9 mg and 18 mg on Quality of Life (QoL) as measured by EQ-5D-5L; (c) Assess the effect of Formula IX 9 mg and 18 mg on circulating tumor cells (CTCs); (d) Assess the impact of duration of prior CB on outcome; (e) Assess the impact of time from diagnosis of metastases to randomization on outcome; (f) Describe the effect of Formula IX 9 mg and 18 mg on tumor volumetries; (g) Assess the effect of plasma concentrations of Formula IX and Formula IX glucuronide on CBR at 24 weeks.

[000576] The safety objective was to describe the safety profile of Formula IX 9 mg and 18 mg PO daily in subjects with ER+/AR+ BC with centrally confirmed AR+ as well as in all subjects randomized and treated.

[000577] The pharmacokinetic objective: To describe the plasma concentrations of Formula IX and Formula IX glucuronide at each of the assessed time points.

[000578] Formulation, Packaging, and Labelling: Formula IX 3.0 mg Softgels were supplied as opaque, white to off-white, size 5, oval Softgel capsules containing 3.0 mg of Formula IX. The liquid Softgel fill was composed of Formula IX dissolved in polyethylene glycol 400. Formula IX 3.0 mg Softgels were packaged in blister packs. Each blister pack contained sufficient study drug for one (1) week of dosing. At randomization (Visit 2) and at Visits 3, 4, and 5), subjects were provided with a carton of study drug containing 7 blister packs, equivalent to 7 weeks of dosing. At Visits 6, 8, 9, 10, 11, 12, and 13, in order to accommodate the visit schedule of every 12 weeks (± 7 days), the subjects received two carton boxes of study drug (each containing 7 blisters) to cover study treatment for 14 weeks. Subjects were requested to bring with them the carton box with all blister packs at every visit.

[000579] Each blister pack was comprised of an appropriate number of blister strips ( 1 blister for the 9 mg treatment arm and 2 blisters for the 18 mg treatment arm) encased in a child- resistant heat-sealed card. The blister strips were composed of a PVC/ACLAR base and an aluminum foil/PVC/PVAC copolymer and polymethacrylate (product contact) lidding. Perforations on the back of the heat-seal card overlay the foil lidding. To remove the study drug, subjects released the appropriate perforation by depressing a release button on the inside of the card. Once released, the perforation can be removed and the study drug pushed through the foil.

Pharmacokinetic assessment:

[000580] Blood samples for pharmacokinetic assessment were collected at baseline (pre-dose), Visit 3 (week 6), Visit 5 (week 18), and Visit 6 (week 24). One blood sample was collected in a 6 mL K2-ethylenediaminetetraacetic acid (EDTA) blood collection tube on each of these days. The exact time (hh:mm) and date that each blood sample was collected was recorded on the electronic Case Repot Form. At the baseline visit, the blood sample was collected before the subject was given their first dose of Formula IX. At Visits 3 (week 6), 5 (week 18), and 6 (week 24), the date and approximate time of the last dose of Formula IX prior to the blood sample should be recorded, i.e., it should be documented whether the subject took the previous dose that morning or the evening before. Immediately after collection, the tubes were gently inverted several times to mix the anticoagulant with the blood sample.

[000581] Blood samples were kept on wet ice (ice packs in a water bath was also acceptable) for up to 20 minutes until processed. The plasma fraction was separated by placing the collection tube into a centrifuge for 10 minutes at 1,500 x g. The plasma fraction was withdrawn by pipette and divided into two 2 mF polypropylene transfer vials (with each tube receiving approximately equal aliquots).

[000582] All sample collection and freezing tubes were clearly labeled in a fashion which identified the subject, the study number, the visit number, and freezing tube aliquot letter. Labels were fixed to freezing tubes in a manner that would prevent the label from becoming detached after freezing. Samples were stored in a freezer at -20°C or lower. Samples were shipped in a thermal insulated container with sufficient dry ice to assure they remain frozen. [000583] Any remaining plasma samples after completion of the protocol outlined pharmacokinetic analysis may be used to identify and quantify the metabolites of Formula IX.

Results

[000584] Table 13 describes a subset of the total number of patients. These were patients that were evaluable (AR+) with measurable disease at study entry and received palbociclib as a previous therapy. Table 13

[000585] According to Table 13, in the 9 mg Formula IX arm, there were 3 patients that previously were treated with palbociclib and failed. Among these 3 patients, one patient (33%) had a complete response (CR). In the 18 mg arm, there were 6 patients that were previously treated with palbociclib and failed. Of these 6 patients, there was one CR and one PR for a response rate of 33%. These data support that Formula IX had activity in patients that were resistant/non-responsive to CDK 4/6 inhibitors.

[000586] Table 14 describes a subset of the total number of patients. These patients on the study had measurable disease at baseline and an AR staining prior to entry into the study. The radiographic imaging in this patient population was done every 12 weeks (2.7 months). Therefore, the minimum radiographic progression free survival (rPFS) that could be determined is approximately 2.7 months. 90% of the patients in the study had previously received non-endocrine based chemotherapy. The patients in this study had failed an average of 2 prior treatment lines for metastatic disease (range = 0-5). Figure 43 provides a scatterplot for the patients in this study with regard to the correlation between % AR-positive staining at baseline (% AR staining) and rPFS. As can be seen in the figure, for patients with <40% AR staining progression was seen at the first time point of 2.7 months or 12 weeks, i.e., rPFS of 2.7, indicating that Formula IX had little to no efficacy in delaying progression in these patients. However, in patients with greater than or equal to 40% AR-positive staining, the rPFS was delayed to variable extents (scatter plot pattern) in many to most cases. A positive correlation between rPFS and % AR staining was seen above the threshold of 40% AR staining. To explore this positive correlation further, several subgroups of AR % staining were defined and analyzed for metrics of efficacy, as shown in Table 14.

Table 14: 9 mg dose group (measurable disease at baseline) PR=partial response, SD=stable disease, AR=androgen receptor, rPFS=radiographic progression free survival

[000587] As shown in Table 14, there appears to be a relationship between % AR staining and clinical response (efficacy) to SARM treatment. Many of the patients typically categorized as AR-positive, i.e, with AR % staining of greater than 1%, did not benefit from SARM therapy. It appears that low levels of AR % staining is not sufficient to observe a clinical response. Unexpectedly, efficacy was predominantly in tumors with high levels of % AR staining. For example, groups of patients with <20%, 20-40%, and <40% AR staining had 0% objective response rate (ORR), whereas all groups inclusive of greater than or equal to 40% AR staining demonstrated a measurable ORR. E.g., groups with >40% had an ORR of 48% and average rPFS of 7.15 months compared 0% and 2.7 months for <40%. This ORR of 48% indicates that tumors shrank >30% (PR) or disappeared (CR) as determined radiographically in about half of these subjects (see RECIST criteria). The observation of objective responses only in patients with >40% AR staining suggests this value as a threshold for prescreening patients for SARM therapy. Clinical benefit response rate (CBRR; another metric of efficacy that includes SD), was also much higher for patients with >40% AR staining compared to patients with <40% AR staining (80% vs. 18%) indicating that only 20% of patients in the higher AR staining group did not achieve some clinical benefit. rPFS measures the efficacy in terms of ability to delay progression of disease. rPFS seems to be loosely correlated with the % AR staining as >40%, >60%, and >80% demonstrated 7.15 months, 8.14 months, and 8.18 months of rPFS. These rPFS values are each more than twice the rPFS for the <40% group (2.70 months), again, suggesting that >40% AR staining could be used as a threshold to prescreen patients that will benefit from SARM therapy.

Studies Provided Rationales for Enriching CBR Based on Screening for >40% AR Staining

[000588] Enobosarm has an extensive clinical experience with 25 clinical trials conducted under sponsor- initiated INDs submitted to FDA with 1,450 subjects being dosed with enobosarm. In breast cancer, four Phase 2 studies were conducted of which two Phase 2 clinical studies conducted under sponsor-initiated INDs submitted to FDA were in women who had AR+ER+HER2- metastatic breast cancer in 158 subjects.

[000589] The first Phase 2 clinical trial (G200801) was a single arm study evaluating 9 mg oral daily dose of enobosarm in a heavily pretreated estrogen blocking resistant cohort of 22 subjects with AR+ER+HER2- advanced breast cancer. Average previous lines of estrogen blocking therapies were 4 (range 1-5) and 68% had previous chemotherapy. The clinical benefit rate at 6 months was 35.3% (90% Cl: 16.6%, 58%). Progression free probability was 57.5% at Day 84 and 50.5% at Day 168. The 6-month Kaplan-Meier estimate for radiographic progression free survival was 43.8%. Enobosarm was well tolerated without evidence of virilization, increase heamatocrit or liver toxicity.

[000590] The second Phase 2 clinical trial (G200802) was a 2-arm study evaluating 9 mg and 18 mg enobosarm daily oral dosing in 136 women with ER+HER2- advanced breast cancer. The patients in this study were also heavily pretreated having experienced disease progression on an average of 3 estrogen blocking agents and 90% had received prior chemotherapy. Enobosarm showed efficacy activity with a clinical benefit rate at 6 months: 9 mg was 32% (95% Cl: 19.5%, 46.7%) and 18 mg was 29% (95% Cl: 17.1%, 43.1%). Median duration of clinical benefit was not reached in the 9 mg group (8.2 month-Not reached) and for 18 mg group was 14.1 months (11 months-16.5 months). Best overall objective tumor response rate based on RECIST 1.1 and central read in all evaluable patients: 9 mg was 3 CR and 8 PR and 18 mg 1 CR and 5 PR (post-hoc analysis). Quality of life assessments showed significant improvement from baseline for both the 9 mg and 18 mg enobosarm cohorts (p=0.002) especially for improvements in mobility, anxiety, and pain discomfort. Enobosarm was well tolerated at both the 9 mg and 18 mg doses.

[000591] In a post-hoc analysis in patients receiving the 9 mg dose during the study, the efficacy of enobosarm in patients with an AR nuclei staining >40% was compared to patients with an AR nuclei staining <40% was assessed (see Table 14 above). The observations from this analysis were:

(i) There is a clear difference in treatment effect in patients with an AR nuclei staining >40% compared to patients with an AR nuclei staining <40%.

(ii) The ORR in patients in patients with an AR nuclei staining >40% is 48% (12/25) and 0% (0/22) in patients with an AR nuclei staining <40%. This finding is statistically significant with a p=0.0001 (Fisher’s exact test)

(iii) The median duration of response in the patients with an objective tumor response is 8.18 months (range 2.73 to >27.83 months) with 67% of the responders had a duration of response >6 months and 25% of the responders had a duration of response >12 months.

(iv) The rPFS in patients with an AR nuclei staining >40% was 5.47 months and 2.72 months in patients with an AR nuclei staining <40%. This finding is statistically significant with ap<0.001.

(v) Further, there appears to be an overall survival advantage for patients with an AR nuclei staining of >40%, as depicted in Figure 45.

[000592] Overall, these studies establish the potential efficacy of a selective AR agonist like enobosarm in the treatment of AR+ER+HER2- metastatic breast cancer with an AR nuclei staining >40%. Examples 32 and 33 provide clinical trial protocols whereby the skilled artisan can make and use the invention in EET and CDKi resistant patients using SARM plus CDKi as 2 ^nd line therapy (Example 32) or 3 ^rd line patients given SARM monotherapy (Example 33).

[000593] Further, these principles as applied to clinical trials in patients treated in the 2 ^nd and 3 ^rd line settings, would also apply to prescreening of patients in the 1 ^st line setting. That is patients who are treatment naive, or hormone therapy naive. Moreover, patients can be selected for SARM therapy for the treatment of a broad spectrum of breast cancers as enabled in the Examples 1-33, not just for AR+ER+HER2- metastatic breast cancer, by first screening for the therapeutic target of AR nuclei staining. Also, although initial clinical trials will employ the cutoff of >40% AR nuclei staining, other cutoff values which are higher or lower than 40% may also be gainfully employed and enrich the ORR and CBR, so long as the cutoff is significantly higher than the 1% used in the clinic to define a breast cancer patient as AR+.

[000594] In addition, the other potential clinical benefits because of tissue selectivity including an increase in muscle and physical function, improvement of bone strength, and lack of androgenic effects including masculinization and increase in hematocrit could be beneficial in this patient population. Targeting the AR in AR+ER+HER2- metastatic breast cancer would allow another novel therapy in the subset of the AR+ER+HER2- metastatic breast cancer population with an AR nuclei staining > 40%.

[000595] In a post-hoc subset analysis from the Phase 2 G200802 study, ten patients who had experienced disease progression on estrogen blocking agents (same as EET described above) and CDK 4/6 inhibitor were evaluable. In this subgroup, 7 of the patients had an AR nuclei staining >40% and 4 patients had an AR nuclei staining >60%. In the >40% group, 3 patients had an objective response (2 CR and 1 PR) and all three of these patients were in the >60% subgroup (75%). Thus, enobosarm alone appears to have antitumor activity in CDK 4/6 inhibitor and EET resistant AR+ER+HER2- metastatic breast cancer.

[000596] Based on these data and the non-clinical data showing that enobosarm in combination with a CDK 4/6 inhibitor in patients that are CDK 4/6 inhibitor resistant, it has been planned to evaluate as 2 ^nd line treatment in the metastatic setting the addition of enobosarm, an AR targeted agonist, in combination with a CDK 4/6 inhibitor (abemaciclib). As discussed below in Example 32, Protocol V2000701 is designed to provide data supporting the safety and efficacy of enobosarm in combination with a CDK 4/6 inhibitor (abemaciclib) versus an estrogen blocking agent in subjects with ER+HER2- metastatic breast cancer that have experienced disease progression on 1 ^st line palbociclib + estrogen blocking agent in patients with an AR % nuclei staining >40%.

EXAMPLE 31

RESENSITIZATION TO CDK 4/6 INHIBITORS BY FORMULA IX (SARM) IN CDK

4/6 RESISTANCE MODELS

[000597] Many of the examples above cumulatively provided clinical studies and preclinical studies with clinically relevant in vitro and in vivo model systems to provide strong support for the use of Formula IX in multiple scenarios of advanced ER-positive breast cancer including many models of estrogen endocrine resistance. Further, Example 30 demonstrated that Formula IX maintained activity in patients that were resistant/non-responsive to the CDK 4/6 inhibitor (CDKi) palbociclib. Inhibitors of cyclin-dependent kinase 4/6 in combination with estrogen endocrine therapy have become the standard of care for women with advanced breast cancer and these treatment failures represent a growing unmet need.

[000598] Tissue samples from an ER-positive, PR-negative, and HER2-negative (ER ⁺ , PR-, HER2-) patient that progressed on (i.e., was resistant to) palbociclib were implanted into animal (NSG mice) models and grown as a patient-derived xenograft (PDX). This GAR15-13 PDX model of CDKi resistance was shown to be responsive to Formula IX (SARM) treatment (Figure 44A). Furthermore, as anticipated based upon the patient’s treatment history, they were relatively refractory to palbociclib as a single agent (Palbo). Interestingly, when treated with both Formula IX and palbociclib (Combo), the treatments were synergistic and the tumors basically disappeared. Therefore, Formula IX treatment appeared to re-sensitize this tumor to a drug for which it was previously resistant. This human tumor model also had amplification of the cyclin D1 ( CCNDl ^Amp ) gene which has been implicated as a driver of therapeutic resistance to CDKi. Again, despite this, Formula IX (SARM) is active alone or in combination and further Formula IX re-sensitized tumors to palbociclib. This is also observed in other models tested in vitro including a palbociclib resistant MCF-7 (MCF7 palbo ^R ) line (Figure 44B). MCF7 palbo ^R cells (Palb ^R ) had a compensatory increase in CDK2 expression, indicative of resistance to CDK 4/6 inhibitors but maintained expression of AR and ER comparable to the parental line (data not shown). Lundberg, A. et al. Breast Cancer Res. 21, 34 (2019).

[000599] Figure 44B demonstrated modest activity with either Formula IX alone (SARM) or palbociclib alone (Palbo) in Palb ^R cells but combination therapy (SARM + Palbo) demonstrated synergistic activity in MCF7 palbo ^R cells; providing another model where CDKi resistance can be overcome by Formula IX and palbociclib co-therapy. These findings that Formula IX (SARM) could restore sensitivity to a CDKi in these models of estrogen endocrine and CDKi resistance were important and unexpected findings which expand the scope of ER- positive breast cancers amenable to treatment with Formula IX. For example, this data supports the use of Formula IX alone or in combination with CDKi, and even after the patient has acquired resistance to CDKi and estrogen targeted endocrine co-therapies. Further, CDKi are approved for use with SERMs, aromatase inhibitors, and SERDs (i.e., estrogen endocrine therapy (EET)) such as fulvestrant but eventual treatment failure produces a CDKi and EET resistant population for which few treatment options are available. This data supports use of Formula IX combined with a CDKi in this population, extending the time which ER-positive advanced breast cancers can be treated with hormonal therapies and kinase therapies rather than chemotherapies. Moreover, new evidence is herein provided that Formula IX can be more effective than existing estrogen endocrine therapies or new CDKi (e.g., palbociclib) standard- of-care treatments and, in the case of the latter, can be combined to unexpectedly enhance growth inhibition.

[000600] Examples 32 and 33 provide examples of clinical protocols employing the >40% AR staining as a prescreen before SARM therapy of breast cancer.

EXAMPLE 32

CLINICAL TRIAL PROTOCOL TO OVERCOME CYCLIN-DEPENDENT KINASE 4,6 (CDK4/6) INHIBITOR RESISTANCE EMPLOYING >40% AR STAINING AS A PRESCREEN BEFORE SARM THERAPY

[000601] Breast cancer is heterogenous disease with diverse clinical and molecular characteristics. The initial molecular assessment is to determine hormone receptor status, estrogen receptor (ER) and progesterone (PR), as well as HER-2 status. Estrogen is one of the main drivers of breast cancer proliferation, tumor progression, and metastasis. Consequently, treatments that target the ER are the mainstay of breast cancer therapy, but unfortunately almost all women with metastatic breast cancer will eventually develop resistance to estrogen blocking therapies.

[000602] CDK 4/6 inhibitors have become front line therapy for patients with advanced ER+/HER2- breast cancer when given in combination with an estrogen blocking agent. According to the National Comprehensive Cancer Network (NCCN) guidelines (2020), the category 1 recommendation for ER+/HER2- metastatic breast cancer in the first line setting is nonsteroidal aromatase inhibitor in combination with a CDK 4/6 inhibitor or fulvestrant in combination with a CDK 4/6 inhibitor. In the second line metastatic setting, fulvestrant or aromatase inhibitor monotherapy is recommended; if a CDK 4/6 inhibitor was used in first line. Unfortunately, even with significant tumor efficacy, all patients will eventually progress owing to the development of resistance to CDK 4/6 inhibitors. When there is progression on CDK 4/6 inhibitor therapy, there are limited clinical data to support another CDK 4/6 containing treatment regimen. Current clinical studies suggest, any subsequent fulvestrant treatment for metastatic ER+/HER2- breast cancer after failing one estrogen blocking therapy will have a median PFS range of 4.6-9.3 months with on objective response rate of 10.9%- 21.3% depending on the trial. Alternative treatment approaches are greatly needed.

[000603] The next important alternative therapy for women with breast cancer is to target the AR. 1) AR is the most abundantly expressed steroid receptor in breast cancer being detected between 70 to 95% of breast cancer specimens; 2) There is a high positive concordance rate (70%) between AR positivity in the primary breast cancer and metastases; 3) In both normal breast tissue and in ER+ breast cancer models, androgens and androgen receptor agonists by binding to and activating AR inhibit cellular proliferation; thus, AR is a tumor suppressor; and 4) AR expression in breast cancer specimens predicts favorable disease-free survival and overall survival.

[000604] Targeting AR using synthetic androgens (e.g., fluoxymesterone and medroxyprogesterone acetate) have been shown to have efficacy in the treatment of breast cancer similar to first line tamoxifen. However, the use of synthetic androgens has been limited by their unacceptable side effects including virilization, increase in hematocrit, liver toxicity, and inability to source the drugs.

Target Indication and Pharmacologic Activity

[000605] The target indication is to develop a 2 ^nd line treatment combination for patients with AR+ER+HER2- metastatic breast cancer that have experienced disease progression on 1 ^st line estrogen blocking agent plus palbociclib.

[000606] Enobosarm is a member of a new class of agents called selective androgen receptor modulators (SARM) which means it is both an agonist and an antagonist depending on the tissue type. Enobosarm is an oral daily selective nonsteroidal agonist that targets and activates AR on breast tissue. Enobosarm inhibits AR+ER+ breast cancer proliferation in cell and animal models. Unlike testosterone, enobosarm cannot be aromatized to estrogen. Enobosarm has selective clinical properties that may have potential benefit in women with AR+ER+ breast cancer. For example, preclinical studies have shown that enobosarm builds and heals cortical and trabecular bone with the potential to treat osteoporosis and skeletal related events. Enobosarm has been shown to build muscle and improve physical function in clinical studies in elderly subjects and patients with cancer cachexia including breast cancer. Furthermore, the selectivity of enobosarm results a favorable side effect profile with no masculinization (facial hair and acne), no increase in hematocrit, and no liver toxicity.

[000607] There is strong scientific rationale for combining enobosarm with a CDK 4/6 inhibitor from preclinical studies in cell lines and patient derived xenograft (PDX) models of AR+ER+HER2- breast cancer resistant to CDK 4/6 inhibitor, Palbociclib. First, enobosarm alone suppressed breast cancer cells and PDX tumors that were resistant to both palbociclib and an estrogen blocking agent. Second, the combination of enobosarm + CDK 4/6 inhibitor had an even greater inhibition of breast cancer cells and PDX tumors that were resistant to both palbociclib and an estrogen blocking agent suggesting that enobosarm has the ability to restore CDK 4/6 inhibitor sensitivity.

Summary of Protocol (V2000701)

[000608] A Phase 3 Study to Evaluate the Efficacy and Safety of Enobosarm in Combination with Abemaciclib (Enobosarm Combination Group) compared to Estrogen Blocking Agent (Control Treatment Group) for the Second Line Treatment of ER+HER2- Metastatic Breast Cancer in Patients Who Have Shown Previous Disease Progression on an Estrogen Blocking Agent plus Palbociclib

Primary Objectives:

[000609] STAGE 1: To determine the safety of enobosarm 9 mg once daily (QD) used in combination with a CDK 4/6 inhibitor [Verzenio ^® (abemaciclib) tablets, for oral use, 150 mg twice daily (BID)].

[000610] STAGE 2: To demonstrate the efficacy and safety of enobosarm 9 mg QD in combination with abemaciclib 150 mg BID (Enobosarm Combination Group) versus Estrogen Blocking Agent (Control Treatment Group) in the treatment of estrogen receptor positive (ER+), human epidermal growth factor receptor 2 negative (HER2-), androgen receptor positive (AR+) with a AR% nuclei staining >40% metastatic breast cancer that have previously experienced disease progression on an estrogen blocking agent plus palbociclib as measured by radiographic progression free survival (rPFS). Secondary Objectives:

[000611] The secondary objectives/endpoints of STAGE 2 of this study are:

• Objective Response Rate (ORR), proportion of subjects with a best tumor response of ORR (partial response [PR] or complete response [CR]) on study

• Duration of response in patients that showed an ORR (PR or CR), treatment responders

• Change from baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC - QLQ)

• Proportion of subjects with Clinical Benefit Response (CBR) defined as a CR (at any time during the study), PR (at any time during the study) or Stable Disease (SD) at Day 180

• Assess the change in body composition (total lean body mass, fat mass, and bone mineral density) as measured by dual energy x-ray absorptiometry (DEXA)

• Assess the change in physical performance as measured by Short Physical Performance Battery (SPPB)

• Assess the correlation of the change from baseline in total lean body mass and change from baseline in SPPB at Day 120 and end of study.

• Overall survival Safety Objective:

[000612] STAGE 2: To assess the safety and tolerability of enobosarm in combination with a CDK 4/6 inhibitor, abemaciclib, (Enobosarm Combination Group) versus Estrogen Blocking Agent including, fulvestrant, non-steroidal aromatase inhibitor (AI), or steroidal AI (exemestane with or without everolimus) (Control Treatment Group). Design:

[000613] STAGE 1: This is an open-label safety study of enobosarm 9 mg QD coadministered with a CDK 4/6 inhibitor (abemaciclib), 150 mg BID. [000614] STAGE 2: This study is a multicenter, randomized, open-label, two treatment arm, efficacy and safety study. Subjects will be randomized to the two treatment arms (Enobosarm Combination Group versus Control Treatment Group) in a 1 : 1 fashion. The determination of the treatment to be used in the control arm will be declared prior to randomization.

[000615] If first line of therapy for metastatic breast cancer was a non-steroidal AI plus palbociclib, then the patient will be randomized to either enobosarm + abemaciclib OR fulvestrant.

[000616] If first line of therapy for metastatic breast cancer was fulvestrant plus palbociclib, then the patient will be randomized to either enobosarm + abemaciclib OR AI (steroidal or non-steroidal). If the patient is randomized to the Control Treatment Group to receive steroidal AI (exemestane), the patient may receive exemestane with or without everolimus.

[000617] The primary efficacy endpoint of the study will be the median rPFS.

[000618] Subjects will continue study treatment until disease progression confirmed by blinded independent central reader (BICR) is observed. A safety follow up visit will occur approximately 30 days after last dose of study drug.

Subjects:

[000619] STAGE 1: 3 subjects will be dosed with enobosarm 9 mg QD + abemaciclib 150 mg BID. Only those subjects with documented evidence of AR+ER+HER2- metastatic breast cancer with an AR% nuclei staining >40%, as confirmed by central laboratory, will be enrolled. If no significant safety observations are made with the enobosarm 9 mg QD dose + abemaciclib 150 mg BID, then the 9 mg dose will be utilized in STAGE 2 of this study. If significant treatment related safety observations are identified with the endobosarm 9 mg QD dose + abemaciclib 150 mg BID in one subject, then an additional 3 subjects will be dosed with enobosarm 9 mg QD dose + abemaciclib 150 mg BID dose. If there are significant safety observations identified in 2 patients in any combination treatment, then the study will be suspended.

[000620] STAGE 2: Approximately, 180 subjects are planned to be randomized at a 1:1 ratio into two treatment arms (approximately 90 subjects in each treatment arm). Only those subjects with documented evidence of AR+ER+HER2- metastatic breast cancer with an AR% nuclei staining >40%, as confirmed by central laboratory, will be enrolled. Randomization will be stratified by AR% nuclei staining >60% versus <60% such that each treatment group will have the same number of subjects with AR nuclei staining >60%. Randomization will be stratified by estrogen blocking agent used in first line such that each treatment group will have the same number of subjects receiving fulvestrant + palbociclib as first line. Treatments:

[000621] STAGE 1: Enobosarm 9 mg QD will be administered each day by mouth and abemaciclib will be administered by mouth at a dose of 150 mg BID.

[000622] STAGE 2: Subjects in the Enobosarm Combination Group will receive enobosarm 9 mg QD each day by mouth and abemaciclib 150 mg BID by mouth until disease progression is observed and confirmed by BICR.

[000623] Subjects in the Control Treatment Group will receive a steroidal or nonsteroidal AI (exemestane with or without everolimus) OR fulvestrant approved for the treatment of metastatic breast cancer and is part of the standard of care at the clinical study site until disease progression is observed and confirmed by BICR. The decision of which comparator treatment will be used will be made prior to randomization.

[000624] Procedures (STAGE 1, STAGE 2):

[000625] Potential study participants will undergo a series of screening evaluations including collection of demographic information, acquisition of archival tumor tissue (or fresh biopsy if the aforementioned are not available to send to central lab for AR testing required to determine eligibility and stratification), vital signs including weight, height, body mass index (BMI), blood pressure, pulse, temperature, medical history, physical exam, Eastern Cooperative Oncology Group (ECOG) performance assessment, concomitant medications, and 12-lead electrocardiogram (ECG) within 45 or 30 days prior to randomization. Subjects who give written informed consent and satisfy the selection criteria will be enrolled into the study. [000626] Tissue collection for AR testing: collect paraffin embedded or formalin fixed tumor tissue for central laboratory confirmation of AR status and molecular subtyping. Metastatic tumor tissue is preferred when possible. Archival tissue collected up to 24 months prior to screening may be used in the AR testing. NOTE: If archival tissue is not available a fresh biopsy can be performed if there is an accessible lesion that can be safely biopsied, and the subject is willing. If a fresh biopsy is taken, this should be done prior to randomization into the study.

[000627] Imaging will be conducted at baseline (within 30 days prior to first dose on Day 1), Day 60, Day 120, Day 180, Day 240, Day 300, and every 90 days thereafter and will include computerized tomography (CT), or magnetic resonance imaging (MRI) and bone scan. EORTC-QLQ will be conducted at baseline, Day 30 and every visit thereafter. Pharmacokinetic (PK) sample (sparse) will be taken at every visit in the Enobosarm Combination Group. The sample will be assessed for enobosarm levels. The time the sample is taken and the time of the previous dose of each study drug will be recorded.

[000628] Safety evaluations will be the following:

[000629] Vital signs (temperature/pulse/blood pressure [supine position, if possible])- baseline, every 30 days while on study, and follow up visit. Body weight - baseline, every 30 days while on study, end of study, and follow up visit. ECOG performance status - baseline, every 30 days while on study, and end of study, and follow up visit. Physical examination - baseline, every 30 days while on study, and end of study. Assessment of adverse events - every visit. Record concomitant medications and non-medication therapies - every visit. 12-lead electrocardiogram (single) - baseline and end of study. For the estrogen blocking agent (AI and fulvestrant) and abemaciclib, the approved prescribing information should be followed for any specific safety monitoring in patients receiving the approved product in this study, this includes reduction in dose due to tolerability issues, if indicated.

[000630] Clinical laboratory results:

• Urinalysis - baseline, end of study

• Hematology - baseline, every 90 days while on study, and end of study

• Serum chemistry - baseline, every 30 days while on study, and end of study

• Urine pregnancy test (performed by local lab)- screening only and only for premenopausal or perimenopausal subjects

• Prothrombin time (PT)/International Normalized Ratio (INR) (screening only)

• Activated partial thromboplastin time (aPTT) (screening only)

[000631] DEXA scans - baseline, Day 120 and end of study. SPPB - baseline, Day 120 and end of study. In the Control Treatment Group and for the abemaciclib used in the Enobosarm Combination Group, the approved prescribing information should be followed for any specific safety monitoring in patients receiving the approved product in this study, this includes reduction in dose due to tolerability issues, if indicated. Long term survival follow up - every 30 days after last dose of study drug for 1 year and then every 90 days thereafter.

EXAMPLE 33

CLINICAL TRIAL PROTOCOL TO EMPLOYING >40% AR STAINING AS A PRESCREEN BEFORE SARM MONOTHERAPY

[000632] ARTEST - A Randomized Phase 3 Study to Evaluate the Efficacy and Safety of Enobosarm Monotherapy Versus Active Control for the Treatment of AR+/ER+/HER2- Metastatic Breast Cancer in Patients with Androgen Receptor Nuclei Staining >40% Who Have Shown Previous Disease Progression on a Nonsteroidal Aromatase Inhibitor, Fluvestrant and CDK 4/6 Inhibitor.

[000633] Primary Objectives: To demonstrate the efficacy of Enobosarm in the treatment of androgen receptor positive (AR+) and estrogen receptor positive (ER+) metastatic breast cancer (MBC) as measured by radiographic progression free survival (rPFS). [000634] Secondary Objectives:

• Objective Response Rate (ORR), proportion of subjects with a best tumor response of ORR (partial response [PR] or complete response [CR]) on study

• Duration of response in patients that showed an ORR (PR or CR), treatment responders

• Overall survival

• Change from baseline in physical performance as measured by Short Physical Performance Battery (SPPB)

• Change from baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC - QLQ)

• Proportion of subjects with Clinical Benefit Response (CBR) defined as a CR (at any time during the study), PR (at any time during the study) or Stable Disease (SD) at Day 180

[000635] Safety Objective: To assess the safety and tolerability of enobosarm

[000636] Design: This study is a multicenter, randomized, open-label, two treatment arm, efficacy and safety study. Subjects will be randomized to the two treatment arms in a 1:1 fashion. The primary efficacy endpoint of the study will be the median rPFS. Subjects will continue study treatment until disease progression confirmed by blinded independent central reader (BICR) is observed. A safety follow up visit will occur approximately 30 days after last dose of study drug. Thereafter, survival follow up will be completed monthly for one year. Survival follow up my be completed by phone or records review. After one year, survival follow up will be completed every 90 days.

[000637] Subjects: Approximately, 210 subjects are planned to be randomized at a 1:1 ratio into two treatment arms (approximately 105 subjects in each treatment arm). The subjects with documented evidence of AR+/ER+/HER2- metastatic breast cancer with an AR% nuclei staining >40%, as confirmed by central laboratory, will be enrolled. Randomization will be stratified by AR% nuclei staining >60% versus <60% such that each treatment group will have the same number of subjects with AR nuclei staining >60%.

[000638] Treatments: Subjects in the Enobosarm Treatment Group will receive enobosarm 9 mg QD each day by mouth until disease progression is observed and confirmed by BICR. Subjects in the Control Treatment Group will receive an estrogen receptor targeted limited to exemestane monotherapy, exemestane plus everolimus, or selective estrogen receptor modulator approved for the treatment of breast cancer and is part of the standard of care at the clinical study site until disease progression is observed and confirmed by BICR. The decision of which comparator treatment will be used will be made prior to randomization·

[000639] Procedures: Potential study participants will undergo a series of screening evaluations including collection of demographic information, acquisition of archival tumor tissue (or fresh biopsy if the aforementioned are not available to send to central lab for AR testing required to determine eligibility and stratification), vital signs including weight, height, body mass index (BMI), blood pressure, pulse, temperature, medical history, physical exam, Eastern Cooperative Oncology Group (ECOG) performance assessment, concomitant medications, and 12-lead electrocardiogram (ECG) within 45 days prior to randomization. Subjects who give written informed consent and satisfy the selection criteria will be enrolled into the study.

[000640] Tissue collection for AR testing: collect paraffin embedded or formalin fixed tumor tissue for central laboratory confirmation of AR status and molecular subtyping. Metastatic tumor tissue is preferred when possible. Archival tissue collected up to 24 months prior to screening may be used in the AR testing. NOTE: If archival tissue is not available a fresh biopsy can be performed if there is an accessible lesion that can be safely biopsied, and the subject is willing. If a fresh biopsy is taken, this should be done prior to randomization into the study.

[000641] Imaging will be conducted at baseline (within 30 days prior to first dose on Day 1), Day 60, Day 120, Day 180, Day 240, Day 300, and every 90 days thereafter and will include computerized tomography (CT), or magnetic resonance imaging (MRI) and bone scan. SPPB will be conducted at baseline and every 60 days while on study, and end of study. EORTC- QEQ will be conducted at baseline, every 30 days while on study, and end of study. Pharmacokinetic (PK) sample (sparse) will be collected at baseline and every 30 days while on study in the Enobosarm Treatment Group. The time of sample and time of previous dose of enobosarm will be recorded.

[000642] Safety evaluations will be the following:

• Vital signs (temperature/pulse/blood pressure [supine position, if possible])- baseline, every 30 days while on study, and end of study.

• Body weight - baseline, every 30 days while on study, and end of study.

• ECOG performance status - baseline, every 30 days while on study, and end of study.

• Physical examination - baseline, every 30 days while on study, and end of study.

• Assessment of adverse events - every visit.

• Record concomitant medications and non-medication therapies - every visit.

• 12-lead electrocardiogram (single) - baseline and end of study.

[000643] Clinical laboratory results:

• Urinalysis - baseline, end of study

• Hematology - baseline, every 90 days while on study, and end of study

• Serum chemistry - baseline, every 30 days while on study, and end of study

• Urine pregnancy test (performed by local lab)- screening only and only for premenopausal or perimenopausal subjects

• Prothrombin time (PT)/International Normalized Ratio (INR) (screening only)

• Activated partial thromboplastin time (aPTT) (screening only)

[000644] In the Control Treatment Group, the approved US FDA prescribing information should be followed for any specific safety monitoring in patients receiving US FDA approved product in this study, this includes reduction in dose due to tolerability issues, if indicated. [000645] While certain features of the invention have been illustrated and described herein, many modifications, substitutions, changes, and equivalents will now occur to those of ordinary skill in the art. It is, therefore, to be understood that the appended claims are intended to cover all such modifications and changes as fall within the true spirit of the invention.