The present invention relates generally to an apparatus and method for control of a hyperthermia patient treatment protocol. More particularly the inven- tion relates to a novel apparatus and method for control¬ ling a hyperthermia treatment device by real time opera¬ tor adjustment of energy input to portions of the patient's body after operator evaluation of the video presentation of correlative temperature data from treated portions of the patient's body. The invention is further related to the accumulation of a hyperthermia treatment data base and for assessing relative figures of merit for different hyperthermia treatment protocols.

Hyperthermia treatment of cancerous tumors is a relatively new method of destruction of cancerous growths within a patient's body. Various systems have been developed to selectively heat the cancerous growths by using electromagnetic radiation and more recently by using ultrasound energy. In order to attain optimum effectiveness in hyperthermia treatment, the apparatus should be able to characterize and to document the tem¬ perature distribution associated with the tumor itself and with normal tissue surrounding the tumor. Further¬ more, it is desirable to have the ability to display to the operator in the most effective manner the ongoing thermal treatment to enable optimization of the treatment to attain a predetermined temperature protocol. Previous apparatus and methods for hyperthermia treatment have attempted to characterize the thermal treatment by dis- playing tables of tumor location, temperature and time of treatment or alternatively by displaying plots of the temperature versus time of treatment for the temperature sensors. The association of each of the sensors with a particular time-temperature plot has been accomplished by color coding of the line of the plot to the associated temperature sensor. (See, for example, the brochure entitled "BSD-aoO" , BSD Medical Corporation, Salt Lake,

Utah) . Prior hyperthermia apparati have also generally utilized only a single one of a plurality of temperature sensors to provide a feedback signal to control the tem¬ perature of the entire tumor (see, for example, brochures entitled, "Astra 200", Oncotherm, Inc., Los Angeles, California; and, the brochure entitled, "Modular Approach Provides Easy Expansion of Hyperthermia Capability"; from Clini-Therm Corp., Dallas, Texas).

BRIEF SUMMARY OF THE INVENTION A primary object of the invention is to provide an improved apparatus and method for control of a hyper¬ thermia patient treatment device.

A more particular object of the invention is to provide a novel apparatus and method for real time opera- tor control of hyperthermia treatment using a video pres¬ entation of correlative temperature data and applied energy for treated portions of the patient's body.

Another object of the invention is to provide an improved apparatus and method for accumulation of a data base of patient treatment history for a variety of locations, sizes and types of tumors.

A further object of the invention is to provide a novel apparatus and method for generating video presen¬ tations of a plurality of topographical maps of isother- mal temperatures for different depths in the vicinity of a tumor in a patient's body.

An additional object of the invention is to provide an improved method and apparatus for preparing predetermined hyperthermia treatment protocols and for adapting an ongoing treatment using a hyperthermia treat¬ ment data base accumulated by controlling the treatment using a video presentation of correlative temperature data and applied energy for treated portions of a patient's body. Another object of the invention is to provide a novel apparatus and method for preparing a predetermined hyperthermia treatment protocol for a ^" tumor in a

patient's body by mapping data in a hyperthermia treat¬ ment data base to identify tumor characteristics similar to the patient's tumor and modifying the data base proto¬ col to develop the predetermined protocol. A further object of the invention is to provide an improved apparatus and method for determining a figure of merit for a hyperthermia treatment to enable charac¬ terization of therapeutic results of the treatment and to allow real time modification of an ongoing treatment to improve the therapeutic results.

Further objects and advantages of the present invention, together with the organization and manner of operation thereof, will become apparent from the follow¬ ing description of the invention when taken in conjunc- tion with the accompanying drawings wherein like refer¬ ence numerals designate like components throughout the several figures.

BRIEF DESCRIPTION ^' OF THE DRAWINGS FIGURE 1 is a block diagram of an apparatus for hyperthermia treatment of patient tumors under control of an operator;

FIGURE 2 is a functional block diagram showing the data flow among software programs (modules) for the hyperthermia treatment apparatus; FIGURE 3 illustrates a video presentation of a grid within which is delineated an outline of a tumor with the location of temperature sensors shown as num¬ bers;

FIGURE 3B illustrates a video presentation of a grid area corresponding to the area of FIG. 3 with each of sixteen indicated grid area elements capable of re¬ ceiving selected percentages of energy from an applica¬ tor;

FIGURE 3C illustrates a video presentation of selected temperature correlative data wherein predeter¬ mined temperature threshold zones are each associated with a preselected color;

FIGURE 4 illustrates a video presentation of the time-temperature history of minimum and maximum tem¬ peratures attained among temperature sensors within each of the two groups of sensors in the tumor region and in the normal tissue region;

FIGURE 5 illustrates a video presentation of the time-temperature history for the temperature sensors positioned within the associated four quadrants of the grid shown in FIG. 3A; and FIGURE 6 illustrates the functional dependence of a linear and a typical non-linear time-temperature dependent function used to predict treatment temperature at a future time.

DETAILED DESCRIPTION Broadly stated the present invention is a sys¬ tem which cooperates with an operator to control a hyper- ^' thermia patient treatment device by using a video display presentation of correlative temperature data from the region of the patient's body undergoing treatment to enable the operator to adjust energy input to optimize treatment conditions. The video presentation includes a prompt signal from a computer to request operator consid¬ eration of whether adjustment of the energy input is necessary to achieve a predetermined time-temperature protocol. Alternatively, the system can operate in an automatic mode with operator interaction limited to emer¬ gency intervention and monitoring of the treatment proto¬ col.

The correlative temperature data includes a display on a grid of the spatial location of color coded temperature sensors with respect to the displayed tumor outline which has been calculated from information input by the operator. The correlative temperature data fur¬ ther includes a second display of the same grid area as the sensor location grid but shows the energy input power level in each of a plurality of subelements of the grid. An accompanying display illustrates by a color

coded bar graph the temperature level for each of the plurality of temperature sensors. The bar graph tempera¬ ture display is separated into two groups with one group associated with temperatures in the normal tissue and another group associated with temperatures in the treat¬ ment or therapeutic region of the tumor.

A color coded scale is preferably positioned between the two groups of bar graphs. The color coded scale for the normal tissue region is divided into two color zones, a substantially safe zone and a substantial¬ ly harmful zone. The color coded scale for the tumor region is divided into three color zones, including a lower zone, a preferred treatment zone and an upper zone. An additional real time display of correlative temperature data includes maximum and minimum tempera¬ tures reached as a function of treatment time among all temperature sensors within each of the two groups of sensors in the tumor and in the normal tissue regions. This information is also stored in memory, and the ther- mal treatment history is documented by storing .the cor¬ relative temperature data, the applied energy data and various characteristic features of the data, such as figures of merit. This thermal history information can be used in real time to modify the treatment to achieve the optimum results. After patient treatment the informa¬ tion can be compared in light of the therapeutic results to enable preparation of future predetermined treatment protocols. This thermal treatment history can be further utilized and examined by generating topographical dis- plays of isothermal regions in the vicinity of the tumor. A data base of the patient treatment history and therapeutic results is also accumulated for use in treat¬ ment of other patients.

Referring now to the drawings and in particular to FIG. 1, a block diagram of hardware for a system con¬ structed in accordance with one embodiment of the present invention is indicated generally at 10. The following model numbers of products and equipment represent prefer-

red components although other similar components can be substituted. The hardware 10 includes an applicator means for applying energy to heat portions of the patient's body. The applicator means in the illustrated embodiment is an ultrasound applicator 12 which generates ultrasonic wave energy by applying a high voltage radio frequency (RF) signal to one side of a piezoelectric crystal grounded on a second side of the crystal. The crystal is modulated by the RF signal to generate ultra- sonic waves which are applied to selected areas of the patient's body. In other embodiments of the invention other types of energy, such as microwaves, can be used to heat the patient's body. The applicator 12 is actuated responsive to commands received from computer means, such as a computer 14. In the illustrated embodiment the computer 14 is a Micro-PDP 11 (a trademark of Digital Equipment Corporation) manufactured by Digital Equipment Corporation, Nashua, N. H. As shown in Fig. 1 the ^" com¬ puter 14 inclμdes a number of components, each of which are manufactured by Digital Equipment Corp. The computer 14 includes a KDF11-B central processing unit 16 and a coupled floating point integrated circuit chip 18, KEF11- AA. The computer 14 includes storage means, such as an RD51 Winchester drive mass storage unit 20 with 10 mega- bytes storage and an RX50 floppy disk storage unit 22. Both the Winchester storage unit 20 and the floppy disk storage unit 22 are controlled by an RQDX1 mass storage controller 24. The computer 14 also includes a random access memory 26 (RAM), which in the illustrated embodi- ment is a MSV11-P having 256 kilobytes of storage. Power for the computer 14 is supplied by an H7864 power supply 28. Input/output is accomplished through an interface 30, such as, for example, a DLVJ1 which is a four line asynchronous serial interface, and in the illustrated embodiment is an integral component supplied with the PDP-11. The computer 14 implements a temperature treat¬ ment regimen or protocol in accordance with appropriate protocol data and instructions stored in the floppy disk

storage unit 22 or in the Winchester storage unit 20. In a preferred embodiment the data and instructions are loaded from the Winchester storage unit 20 into the RAM 26, and the computer executes a hyperthermia treatment protocol characterized by the data and instructions stored in the RAM 26. The slower loading floppy disk storage unit 22 is preferably used after completion of the protocol for permanent storage of the measured data from the hyperthermia treatment. The operator interacts with the computer 14 through operator means to supply an operator signal 31 to the computer 14 responsive to an operator input. In the illustrated embodiment, the operator means is a keyboard 32 in FIG. 1, which is part of a video display terminal 34 (for example, a VT 220 from Digital Equipment Corp).

The operator input, or manipulation, is therefore the depression of the keyboard keys, and the keyboard 32

^' generates the operator signal 31 to the ^" computer 14. In another form of the invention the operator means can be a remote interaction device, such as a personal computer- keyboard and/or display keyboard system (not shown) al¬ lowing remote monitoring and control of the treatments. For example, a physician could control implementation of various hyperthermia treatments at a plurality of loca- tions remote from the physician's office.

The ultrasound energy input by the applicator 12 to the treatment area results in an increase in tem¬ perature of ^" the treatment area. This change in tempera¬ ture is detected by a thermometry unit 36, and in a pre- ferred embodiment the thermometry unit 36 is a multi channel system coupled to temperature sensing means, such as copper-constantan thermocouple temperature sensors 38 disposed within the patient's body. The sensors 38 pre¬ ferably are contained within plastic catheters which are placed in the patient's body, and the catheter is with¬ drawn before treatment in order to avoid disruption of the ultrasound heating pattern. Alternatively, hypoder¬ mic needles containing thermocouples can be inserted into

the patient's body. If operating using the microwave energy to heat the patient's body, the needles should be withdrawn to avoid complete disruption of the desired heating pattern. A plurality of the sensors 38 can be disposed within one of the catheters (or if appropriate, the hypodermic syringes) enabling placement of a plural¬ ity of the sensors 38 along a selected line in the patient's body. In other forms of the invention, the temperature sensing means can be thermistors or other suitable temperature sensing devices.

In preparation for performance of the hyper¬ thermia treatment, the operator establishes initial treatment conditions by activating the executive program which invokes the data entry program and guides the oper- ator through the necessary steps for treatment startup. The operator enters, for example, patient history, length of time of treatment and desired temperature threshold values for -the predetermined temperature protocol. This startup information can be stored for later recall and initiation of treatment, or the operator can immediately commence the treatment procedure. In addition, the oper¬ ator enters further information, such as the location of the temperature sensors 38 and whether the sensor 38 is in the tumor region or the normal tissue region. A sepa- rate computer program generates an outline of the tumor region, and the operator is able to choose to enter fic¬ titious temperature sensors to change the outline or can choose to modify this outline using additional available information. Consequently, after this modification the executive program resumes and sequences the operator through the executive program providing the appropriate command requests to provide for various functionality as described in the specification. The executive program can be written in any of a plurality of languages, in- eluding, for example, assembly language, BASIC and FORTRAN; and the executive program can operate under a plurality of commercially available operating systems, such as RSTS, RT-11, iRMX-86, CP/M-86, MS-DOS or UNIX, on

any of the various commercial computer systems.

In another embodiment of the invention, instead of using the executive program, all necessary functions can be provided by a plurality of separate callable soft- ware routines for the operator to call up at his op¬ tion. In such case, there is no need for the executive program.

Control of the treatment temperature is criti¬ cal to achieve the preselected time and temperature protocol desired for most effective patient treatment. Control of the time-temperature protocol is best accom¬ plished by a system wherein the operator observes color coded video presentations of the type depicted in FIGS. 3-5. Display of each of the video presentations is ac- complished by a graphics controller unit 40, such as, for example a VCG-Q/51 manufactured by Peritek Corporation, Oakland, California. The video presentation is displayed on a video display 42, such as an XM-032-13L color moni¬ tor purchased from Grinriell Systems, Inc., San Jose, California. The color images are constructed by the controller unit 40 which receives a digitized video out¬ put 44 from execution of the graphics software program 54. The controller unit 40 converts the digital video output to an analog video output suitable for display on the video display 42. The controller unit 40 has one hundred twenty eight kilobytes of internal memory for storage of the red, green and blue bits which describe each pixel on the video presentation. Further details of operation of a typical form of the controller unit 40 can be obtained from, "Fundamentals of Computer Graphics", J.D. Foley and A. Van Dam, Addison Wesley Co., Reading, MA, 1982, pages 112-136; and from U.S. Patent Nos. 4,121,283; 4,139,838; and 4,213,189 which are incorpora¬ ted by reference herein. The video presentations viewed by the operator contain temperature correlative data characteristic of the treatment time and the temperature at each of the temperature sensors 38. If the temperature falls outside

the desired range of the predetermined temperature proto¬ col, the computer 14 generates a prompt signal which is displayed as an alphanumeric output on the video display terminal 3 . The alphanumeric output typically takes the form of a notice that the temperature will be out of range in a brief period and asks the operator whether manipulation should be performed, such as an adjustment of the level of applied energy. The computer 14 accom¬ plishes this operational sequence by monitoring the tem¬ perature signal from the temperature sensors 38 and by comparing the measured temperature with the desired pre¬ determined temperature protocol, or time-temperature regimen, stored in the RAM 26. If the measured tempera¬ ture indicates an undesired deviation has occurred or is anticipated, the computer 14 calculates a corrective strategy to achieve the predetermined temperature proto¬ col. The computer 14 can, if desired, cause generation of an _. audible sound to alert the operator and request operator approval of the strategy. If the operator agrees with the proposed strategy; the operator enters the appropriate operator signal 31 by the keyboard 32. Alternatively, if the operator decides to override the suggestion of the computer 14, the operator enters the appropriate override operator signal 31 and generates the necessary replacement information to carry out a differ¬ ent schedule of energy input to achieve the predetermined temperature protocol, or regimen of time-temperature treatment. In another embodiment of the invention the system under control of the computer 14 can operate auto- matically without operator intervention except for emer¬ gency situations or for cases where the protocol is un¬ able to achieve the anticipated treatment conditions.

There are also safety features for the hyper¬ thermia treatment device, including an emergency shut off circuit which removes power to the energy applicator. The shut off circuit is activated if the operator does not respond within a reasonable time period to the prompt signal or if the temperatures reach dangerous levels.

The system is able to save the treatment history informa¬ tion and after operator review of the treatment protocol and current history, the treatment can be resumed where it left off. This monitoring and adjustment operation can be further explained by referring to FIG. 2 which illus¬ trates data flow between the various computer software programs or modules. Many of these software programs comprise routine and operational sequences known to those of ordinary skill and are thus functionally explained herein. A program control module 48 is a supervisory type of software program linked with a timer module 46 and controls event, or interrupt, driven and/or program driven invocation of other software programs which are not involved with a data structures module 52. The data structures module 52 holds all the data needed by the various modules shown in FIG. 2 and is a passive module in that the program contains no executable code, only the data. The timer module 46 works with the program control module 48 and provides timing information for the invoca¬ tion of program driven functions. A menu driven data entry module 53 is entirely program driven and obtains from the operator relevant information used to set tem¬ perature threshold levels, place the temperature sensors 38, activate the energy applicator and record the patient treatment history. A communications module 50 handles the transfer of the data and instructions between the computer 14 and the thermometry unit 36, the printer 29, the ultrasound energy controller 41 and the video display terminal 34. The communications module 50 incorporates both program and interrupt driven components. A graphics module 54 is program driven and performs all formatting and updating of the video display 42 for both temperature and energy level information. A energy or heat applica- tion control module 56 is program driven and operates on the temperature signal from the thermometry unit 36 to generate suggested strategies to the operator concerning adjustment of the ultrasound energy levels. The computer

14 interacts with other systems, such as for example, various ones of the modules, to monitor periodically the temperatures responsive to a timer program 46. The timer module 46 utilizes a clock (not shown) which times out to actuate the program control module 48 and causes genera¬ tion of a signal to the communications module 50. The communications program 50 in turn causes sampling of the temperature sensors 38, and the temperature information resides in a data structures module 52. The program control module 48 invokes the graphics module 54 which uses the temperature data in the data structure module 52 to update the video display 42. The graphics module 54 is program driven and includes the program listed in the Appendix which defines the image location and shape on the video display 42. The graphics module 54 also in¬ cludes a vector graphics program to draw the images and is an off-the-shelf package, (CSP-2 provided by Peritek Corp., Oakland, California).

During the hyperthermia treatment the operator therefore observes the updated condition of the correla¬ tive temperature data and responds by entering the opera¬ tor signal 31 via the keyboard 32. The program control module 48 activates the energy applications module 56 to change the level of applied energy to attain the prede- termined temperature protocol. This interactive process then periodically repeats itself to maintain control of the temperature.

In other embodiments of the invention the com¬ puter 14 can be programmed to generate at selected inter- vals a message on the video display terminal 34. This message can inform the operator of the time-temperature state of the temperature sensors 38 and display differ¬ ences from the predetermined time-temperature protocol. For example, at periodic intervals the computer 14 can generate on the video display terminal 34 the sensor number, whether the temperature is from the tumor region or the normal tissue region, the elapsed time and temper¬ ature and the difference in temperature from the desired

predetermined temperature protocol.

The video display presentation of FIGS. 3A-C includes a variety of correlative temperature data which enables the operator to monitor and adjust the applied energy detected by the plurality of temperature sensors 38 in order to achieve the predetermined temperature protocol for optimum therapeutic effect. The operator begins the treatment procedure by placement of the tem¬ perature sensors 38 in the patient's body in the manner described hereinbefore. The spatial location of the tumor should already have been established with reason¬ able accuracy by other means, such as, x-ray radiography or fluoroscopy, or simply by sense of touch to isolate the tumor position if the tumor is near the skin sur- face. The relative spatial locations of the temperature sensors 38 and the tumor should be determined with good accuracy. The relative coordinates of the temperature sensors ^' 38 are then entered by the keyboard 32, and the sensor coordinates are designated as within or outside the tumor region. These sensor coordinates are then illuminated on the video display 42 by placing the asso¬ ciated number of the sensor 38 at that location. An outline of the tumor region is calculated from these sensor coordinates using a software program entered from either the floppy disk storage unit 22 or the Winchester storage unit 20. On the basis of the tumor area within each of the sixteen subelements 58 in the grid of FIG. 3A, another software program calculates the pattern of ultrasound energy which will be applied to the subele- ments 58 to heat the tumor region.

Initially, the energy applicator will generate ultrasound energy at the one hundred percent level be¬ cause it is desirable to reach the optimum temperature threshold zone as quickly as possible to provide the optimum therapeutic result. Furthermore, rapid attain¬ ment of the desired treatment temperature minimizes treatment time for the patient and minimizes both equip¬ ment use time and the operator time per treatment cycle

which contribute to a more efficient process and a more desirable treatment protocol. Once the temperatures begin to approach the desired temperature ranges, the power levels are reduced (as shown in FIG. 3B) to allow steady state, controlled treatment temperatures to be maintain¬ ed. FIG. 3B illustrates another portion of the video presentation which shows a four-by-four array 60 which portrays the subdivision of energy application by the ultrasound applicator. Exemplary applied power or energy levels are indicated numerically in square subelements 62 of FIG. 3B, and the power level is also illustrated by colored bars 64 expandably positioned horizontally or vertically within each of the subelements 62. In other embodiments of the invention, the relative percentages of power can be indicated by a variable size, concentrically expanding square or circle positioned within the subele¬ ments 62.

The correlative temperature data of FIG. 3C includes vertically positioned bar graphs of the tempera- ture at each of the associated temperature sensors 38 with the sensor number indicated at the bottom of each color coded bar 66. Preferably the selected color code comprises a plurality of different colors, but in other embodiments of the invention the plurality of colors becomes a plurality of grey scale values for one selected fundamental color.

The bar graph temperatures have been separated into two groups, one associated with therapeutic tempera¬ tures in the tumor region and another group associated with temperatures in normal tissue. Each of the color coded bars 66 also has a digital readout of the associ¬ ated temperature positioned near the top of each of the bars 66. Toward the bottom of each of the bars 66 is an "icon" or indicator bar 68 which signifies the relative rate of temperature change for the associated temperature sensor 38. In the illustrated embodiment, there are five angular positions for the indicator bar 68, wherein a zero rate of temperature change is indicated by a hori-

zontal position for the indicator bar. For non-zero temperature rates of change, there are two angular posi¬ tions tilted upward and two positions tilted downward from the horizontal position which are indicative, re- spectively, of increasing and decreasing rates of temper¬ ature change. In other embodiments of the invention, the rates of temperature change can be indicated by continu¬ ously variable positions for the indicator bar 68, or by an expanding pie-shaped section or by a concentrically expanding circular or square area disposed within or associated with each of the color coded bars 66.

The two groups of temperature bar graphs shown in FIG. 3C are separated from one another by a color coded temperature threshold scale 70, and the scale 70 itself is divided into a first vertical portion 72 for the treatment, or tumor, region and a second vertical portion 74 associated with the normal tissue region. The second vertical _. portion 74 for the normal tissue region is divided into two temperature threshold zones of pre- selected colors, wherein the colors representing the predetermined temperature threshold zones are changeable by the operator specifying the limits of the zones, pref¬ erably at startup of the treatment. The two zones for the normal time region are: (1) a safe zone 76 having an upper threshold MANT (maximum allowed normal tempera¬ ture), and in this safe zone 76, normal tissue is sub¬ stantially unharmed by the treatment, and (2) a harmful zone 78 above the threshold value MANT wherein normal tissue suffers increasing damage as the temperature in- creases. These two zones can also be referred to as a desirable zone and an undesirable zone, respectively. The first vertical portion 72 for the tumor region is divided into three temperature threshold zones of pre¬ selected colors, and the zone limits are determined by the operator, again preferably at startup: (1) a lower zone 80 wherein tumor tissue is not normally affected, (2) a preferred temperature treatment zone 82 having a lower threshold temperature of MITT (minimum treatment

temperature) and an upper threshold temperature of MATT (maximum treatment temperature), and within the zone 82 the tumor tissue degrades, and (3) an upper zone 84 above the MATT threshold temperature, and within the zone 84 tumor degradation is not nearly as pronounced as in the preferred zone 82 and can result in excessive damage to surrounding normal tissue. In the case of breast tumors, for example, the threshold temperatures values include a value of about 40°C for the MANT, the MITT is approxi- mately 42.5°C and the MATT is about 48°C. These three zones can also be divided into the desirable zone (the zone 82) and the undesirable zone (the zones 80 and 84. It should also be noted that the positioning of these threshold temperatures is somewhat flexible because the hyperthermia treatment is actually a time-temperature treatment such that substantially the same thermal result can be obtained for long term treatments at lower temper¬ atures and for short term treatments at higher tempera¬ tures. Therefore, the above threshold temperatures are nominal values which can be adjusted somewhat depending on the treatment time.

By observing this collective temperature data the operator is able to monitor numerous variables in an efficient manner, including the rate of change of temper- ature with time, the temperatures of the tumor region and normal tissue region and whether or not the temperature of each of the temperature sensors 38, and each group of sensors, is in the optimum temperature threshold zone. Furthermore, FIG. 3A simultaneously displays the spatial location of the temperature sensors 38 with respect to the tumor, and each of the sensor numbers is color coded to the temperature threshold scale 70, enabling correla¬ tion of spatial location to the ongoing therapeutic ef¬ fectiveness of the temperature at that location. The time history of the temperature correlative data displayed in FIGS. 3A-C is preferably stored in the Winchester storage unit 20 or in the floppy disk storage unit 22. This information is also added to the past

history of the patient in order to assess treatment prog¬ ress and prognosis. The temperature correlative data and the associated therapeutic result are also stored in one of the storage means for purposes of accumulating a gen- eral data base of treatment response to obtain statistic¬ ally meaningful information for developing the optimum treatment protocol for a wide range of tumor sizes, loca¬ tions and classes or types (stage of growth). Therefore, a particular protocol can be prepared by mapping data in the data base to determine tumor characteristics corre¬ sponding to the tumor in the patient's body. The proto¬ col in the data base can then be modified to account for differences between the patient and data base tumors to provide the predetermined treatment protocol for the patient.

In a typical hyperthermia treatment procedure, the correlative temperature data for each set of the temperature sensors 38. shown in FIG. 3 . s updated approximately every fifteen to thirty seconds during the startup portion of the treatment due to the reasonably large rate of temperature increase. The frequency of the updating at any time also depends on individual charac¬ teristics of the anatomical site of the tumor, such as proximity to bones or other structures which affect energy absorption in the vicinity of the tumor. Once the temperature approaches the desired steady state level, the correlative temperature data of FIG. 3 is typically updated approximately every two to four minutes since temperature changes occur quite slowly for most treatment conditions. Again however, it should be noted that for treatment of tumors which are closely positioned to bone structure or other masses which preferentially absorb ultrasound energy, the update should be done more fre¬ quently. Similarly if one is using microwave energy, fatty tissue preferentially absorbs microwaves and thus necessitates frequent temperature update. For situations which require only occasional update of the correlative temperature data, the computer 14 is able to devote it-

self to data analysis and generation of information use¬ ful to the diagnostician. Therefore, in one form of the invention the accumulated patient response can be com¬ pared with the general treatment data base to analyze trends in treatment and if necessary prepare a modified form of the predetermined treatment protocol. For exam¬ ple, the ongoing real time patient response can be modi¬ fied in view of an unexpected patient response, such as unpredicted preferential ultrasound energy absorption by a nearly bone structure.

In another embodiment of the invention, the computer 14 can utilize the time-temperature history to prepare color coded topographical maps of isothermal treatment regions as a function of time and of spatial location within and near the tumor. By using a plurality of the temperature sensors 38 inserted along a series of depth positions in the tumor, a three dimensional set of temperatures can efficiently be collected, and an ex¬ panded grid of interpolated temperature can be calcula- ted. A three dimensional form of the topographical maps is then constructed from a set of two dimensional paral¬ lel slices. By appropriate positioning of the tempera¬ ture sensors 38 and by performing suitable interpola¬ tions, the topographical maps can be constructed for planar sections perpendicular to any one of three pos¬ sible dimensions. The resulting topographical maps are viewable one at a time or can be displayed dynamically to view the evolution of the treatment protocol throughout the treatment period. Additional time-temperature history information is obtainable from the video presentation shown in FIG. 4. This shows the maximum and minimum range of tempera¬ tures reached among all ^* of the temperature sensors 38 in each of the two groups of sensors, one group associated with the treatment region and the other group associated with the normal tissue region. An average temperature is also calculated for each group and is a single bold dash¬ ed line appearing within the range of values in each of

the plots for the two groups. Also included in the dis¬ play for comparison purposes is the color coded tempera _¬ ture scale 70 used in FIG. 3C to indicate the various temperature threshold zones. The operator is therefore able to correlate the range of the minimum and maximum temperature values, the time-temperature integrated areas which lie within and which exceed the various temperature threshold zones and the behavior of the average tempera¬ ture value with respect to these temperature threshold zones.

Information from the video presentation can be used as a basis for various figures of merit to evaluate therapeutic effectiveness of treatments, such as for example, by comparing the relative magnitude of time- temperature integrated areas within and outside of the temperature threshold zones. Generally, the term compar¬ ing is meant to include at least calculation of ratios and arithmetic differences and various selected powers of these quantities, such as the square and square root thereof. These figures of merit can also be used to characterize a data base of use in planning future treat¬ ments and to adapt ongoing treatments to obtain more effective treatment results. The amount of deviation from the planned protocol can be another measure of the figure of merit. An additional useful figure of merit is the degree of overlap of the ranges of temperature for the two groups of sensors. This overlap is the dotted area in FIG. 4, and the comparison of the integrated area of the dotted region relative to the total area within the range curves can be used as a figure of merit for evaluating the ef ectiveness of the treatment. Another figure of merit relates to the comparison of the overlap area with the total area which is time bounded by the startup of the hyperthermia treatment and by the end of the overlap area. Additional figures of merit arise from, for example, comparison of selected areas of this time bounded region which also fall within selected ones of the temperature threshold zones. Further, the treat-

ment protocol, the various figures of merit and the ther¬ apeutic results can be stored to accumulate a data base and can be compared with patient response and with other data bases to adjust treatment conditions to improve ongoing, as well as future treatments.

In other embodiments of the invention, other figures of merit can be obtained by determining the per¬ centage of time the temperatures of each of the tempera¬ ture sensors fall within selected ones of the temperature threshold zones. For example, comparing the relative percentages of time within the desirable and the unde¬ sirable zones can yield a figure of merit for evaluating the effectiveness of a particular treatment protocol. Thus, the greater the percentage of time in the desirable zones, the more favorable is the figure of merit.

The time-dependent temperature data history of each of the _ temperature sensors 38 can also be followed by the video presentation portrayed in FIG. 5. The time- temperature data for the sensors 38 located in each of the four rectangular quadrants of FIG. 3A can be included in one video presentation with four plots displayed, each plot congruently associated with its respective quadrant in FIG. 3A. Also included in the figure is the color coded scale 70 of FIG. 3C for comparison of temperature values with the various temperature threshold zones. In another embodiment of the invention, if the sensors 38 are concentrated, for example, in only one or two of the four quadrants, the array of temperature sensors 38 is divided into the four individual plots of FIG. 5 by re- positioning the center of the quadrants at approximately the center of gravity of the clustered sensor loca¬ tions. For the temperature sensors 38 in the reposi- tioned quadrants, the time-temperature plots are gener¬ ated for analysis by the operator. Control of energy input by the ultrasound ap¬ plicator 12 involves use of computer software composed of selected polynomial and transcendental functions to pre¬ dict- the temperature at a future time given the past

shape of a measured time-temperature curve. The nature of the function most useful under any particular treat¬ ment conditions depends on numerous variables such as, for example, tissue makeup, proximity to bone structure and blood flow rates. Consequently, in one embodiment of the invention, a plurality of functions can be made available in the form of computer software programs for fitting measured hyperthermia treatment temperatures and for carrying out selected statistical evaluations, such as least squares fits, to ascertain the most appropriate function to use for predicting temperature at a future time in the treatment. Selection of functions can also be changed for different regimes of the treatment proto¬ col. For example, in the starting phase of the hyper- thermia treatment, the functional behavior will more likely be a quasi-linear behavior as for a first curve 86 shown in FIG. 6, but as the temperature approaches a steady state value, the functional form can assume, -.for example, a more exponential shape, such as a second curve 88 in FIG. 6. The operator will be able to call upon the previously mentioned time-temperature dependent general data base in order to isolate during the treatment the most probable function of use in predicting changes in temperature for selected characteristic tumor conditions. An Appendix is included herewith providing software program listings for use in processing of the correlative temperature data and video display of infor¬ mation in accordance with the invention.