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This study tests whether DCE-MRI parameters obtained from canine patients with soft tissue sarcomas, treated with hyperthermia and radiotherapy, are predictive of therapeutic outcome.
37 dogs with soft tissue sarcomas had DCE-MRI performed prior to and following the first hyperthermia. Signal enhancement for tumor and reference muscle were fitted empirically, yielding a washin/washout rate for the contrast agent, tumor AUC calculated from 0 to 60s, 90s, and the time of maximal enhancement in the reference muscle. These parameters were then compared to local tumor control, metastasis free survival, and overall survival.
Pre-therapy rate of contrast agent washout was positively predictive of improved overall survival and metastasis free survival with hazard ratio of 0.67 (p = 0.015) and 0.68 (p = 0.012) respectively. After the first hyperthermia washin rate, AUC60, AUC90, and AUCt-max, were predictive of improved overall survivaloverall survival and metastasis free survival with hazard ratio ranging from 0.46 to 0.53 (p < 0.002) and 0.44 to 0.55 (p < 0.004), respectively. DCE-MRI parameters were compared with extracellular pH and 31-P-MR spectroscopy results (previously published) in the same patients demonstrating a correlation. This suggested that an increase in perfusion after therapy was effective in eliminating excess acid from the tumor.
This study demonstrates that DCE-MRI has utility predicting overall survivaloverall survival and metastasis free survival in canine patients with soft tissue sarcomas. To our knowledge, this is the first time that DCE-MRI parameters have been shown to be predictive of clinical outcome for soft tissue sarcomas.
Numerous Phase III clinical trials have demonstrated that thermoradiotherapy is superior to radiotherapy alone for achieving local tumor control and in some cases, improving survival. (1 , 2 , 3 , 4 , 5 , 6) It is well known that hyperthermia changes tumor oxygenation, inhibits DNA damage repair, and is directly cytotoxic. (7 , 8) The effects described above are strongly dependent on temperature and duration of heat exposure but which effect dominates in improving tumor control with thermoradiotherapy is not known. In pre-clinical models, mild to moderate heating (41–43°C) leads to increased perfusion and oxygenation, whereas higher thermal exposures can cause vascular damage and hypoxia. (8) Presumably, this latter effect would be deleterious to optimal thermoradiotherapy response, but there are no definitive clinical studies demonstrating this.
Previous work with canine sarcomas have reported improved oxygenation following a single hyperthermia treatment when median temperatures were less than 44°C (9) and that changes in oxygenation can persist throughout a course of fractionated thermoradiotherapy. (10) Panjapour et al. reported that perfusion was improved throughout a course of thermoradiotherapy in dogs with mast cell tumors. (11) These data support the notion that part of the effect that mild hyperthermia has in improving radiotherapy response is due to increased oxygenation through improved perfusion. However, in neither of these reports was there a correlation made between changes in pO2 or perfusion and treatment outcome.
Brizel et al. reported that improvements in oxygenation 24 hr after the first hyperthermia treatment were associated with higher pathologic complete response rates after thermoradiotherapy of human soft tissue sarcomas. (12) Jones et al. presented similar data in a small series of 13 patients with locally advanced breast cancer who were treated with a combination of hyperthermia, paclitaxel and radiotherapy. (13) The response endpoints reported in both of these studies were relevant to short term cell killing, but neither addressed the more important issue of the effects of reoxygenation on local tumor control.
Because of the importance of perfusion in cancer therapy (with or without hyperthermia), Dynamic Contrast Enhanced-MRI (DCE-MRI) has been gaining use to obtain physiological information. This imaging method provides information related to perfusion and permeability-surface to volume product of a region/voxel of interest.
Recently we reported results from a randomized phase II clinical trial involving thermoradiotherapy treatment of canine soft-tissue sarcomas. (3) Results of this trial indicated that higher thermal dose was associated with significant prolongation of progression free survival. Extracellular pH and 31-P MRS parameters were associated with metastasis free and overall survival in a subset of patients from this same trial. (14) In this particular study we evaluate the potential of DCE-MRI derived parameters, obtained before treatment and 24 to 72 hours post first hyperthermia treatment, to be prognostically predictive in subset of 37 patients who were evaluated with MRI as part of this trial.
Thirty-seven canine patients with spontaneously-occurring soft tissue sarcomas were randomized to receive either a low (2–5) or high (20–50) thermal dose quantified as cumulative equivalent minutes that the T90 was equal to 43°C (CEM43°CT90), in combination with fractionated radiotherapy (56.25Gy in 25 daily fractions of 2.25Gy). T90 refers to the temperature reached or exceeded by 90% of measured temperature points. Tumor types included 20 hemangiopericytomas (54.1%), 9 fibrosarcomas (24.3%), 4 myxosarcomas (10.8%), 2 neurofibrosarcomas (5.4%), and 2 non-specific sarcomas (5.4%). Classification of histologic subtype was performed by a board certified veterinary pathologist. (15) Hyperthermia was induced using microwave applicators operating between 140 and 433 MHz. Thermal dose randomization was stratified by tumor volume and tumor grade. Approximately one hyperthermia treatment was given per week, after the daily radiation fraction. The duration of the hyperthermia treatment was adjusted so as to administer approximately 20% of the prescribed hyperthermia total dose in each hyperthermia fraction. Occasionally the prescribed thermal dose was administered in 4 weekly treatments, and in some other dogs, a 6th treatment had to be added to reach the prescribed thermal dose (3) Magnetic resonance imaging was performed before and 24–72 hours after the first hyperthermia treatment (Figure 1).
The procedures were approved by the North Carolina State and Duke University Animal Care and Use Committees.
All studies were performed on a GE 1.5T Signa System equipped with a surface coil. Dogs were anesthetized with isoflurane (Abbott Laboratories, N Chicago, IL) for the MR study. Coronal and axial localizer images (fast spoiled gradient recalled echo pulse sequence) were acquired initially to define tumor position. Five baseline scans consisting of fifteen T1-weighted images (TR = 400, TE = 15) per volume were acquired before contrast injection (field of view = 256×128, slice thickness = 5–10mm). Subsequently, an intravenous bolus injection (0.1 mmol/kg, 2ml/sec) of Gadolinium dimeglumine (Gd-DTPA) was administered. Image volumes were acquired every 30 seconds for 20 minutes.
Relative enhancement images were fitted pixel-by pixel with a double exponential equation (equation1) using a non-linear iterative Chi square minimization technique based on the marquadt algorithm.
Each fitted curve allowed the extraction of Smax (relative maximal enhancement constant), alpha (delivery rate constant) and beta (clearance rate constant) parameters. Negative values or values from the fit that never converged were not included for calculations of region of interest analysis. These parameters allowed the calculations of washin rate (Smax * alpha), washout rate (Smax * beta) along with area under the signal enhancement curve (AUC). With these parameters descriptors of perfusion/permeability were obtained. (16, 17) For evaluation of AUC, three different integration times were chosen for calculation, AUC 60 (integration time from 0 to 60 seconds), AUC 90 (integration time from 0 to 90 seconds), and AUC t-max (integration time from 0 to when the muscle reference signaled peaked, t-max). Time to maximal muscle enhancement was calculated by setting the derivative of equation 1 to zero and solving for time. Otherwise this last value was used as the upper limit for calculating AUC t-max. Representative patient image data is shown in Figure 2 for pre and post hyperthermia images and pseudo false color for washin, washout, and AUCt-max data.
From the fitted data, region of interest for tumor (including any necrosis) and muscle were manually drawn on each slice to form volumes of interest. Tumor region of interest included the entire tumor and potential necrosis and the muscle region of interest was drawn on muscle free of tumor in the field of view based on known normal anatomy. Median values were extracted from each volumes of interest. Washin, washout, AUC 60, AUC 90 and AUC t-max parameters were analyzed individually. This yielded five different parameters relating to perfusion/permeability. All imaging analyses were made with a custom made software running on MATLAB (The Mathworks, Inc., MA).
Extracellular pH measurements were made using needle microelectrodes ((Microelectrode, Inc., Londonderry, NH; Agulian, Hamden, CT), as previously described . Multiple measurements were made and averaged to obtain an overall estimate of the extracellular pH. Intracellular pH was determined by the frequency difference between the Pi and PCr resonances., from 31-P MRS spectra. MRS Spectra were acquired with a surface dual frequency coil array and triphenyl phosphite standards solutions were placed next to the tumor for pulse calibration. Pulse sequence protocol and data analysis methods have been previously reported in detail (14) (18)(2),
After treatment, dogs were reevaluated at 1, 2, 3, 5, 7, 9 and 12 months, and then at 3-month intervals. Reevaluation consisted of physical examination, tumor measurement, thoracic radiographs and assessment of regional lymph nodes. Tumors volumes were determine by direct physical measurements along 3 axis multiplied together with PI/6. Duration of local tumor control was defined as the time from date of the first hyperthermia treatment until local failure. Metastasis-free survival was defined as the time from date of the first hyperthermia treatment until metastasis or death, and overall survival was the time from date of the first hyperthermia treatment until death from any cause. Spread to regional lymph nodes was classified as positive for metastasis, as well as any spread to distant organs, such as the lung.
Values of area under the curve were Log transformed due to the large range of calculated values, therefore throughout the paper AUC values reported will correspond to Log10(AUC) values.
Each perfusion parameter was assessed for its predictive properties on metastasis free survival, time to local failure, and overall survival overall survival, before and after treatment, as well as their difference post - pre (Δ) treatment, using Cox proportional hazard ratio and Log Rank tests. The effect of the first hyperthermia treatment, as described by T50, T90, CEM43°C T50 and CEM43°C T90 along with administration time of hyperthermia on perfusion parameters obtained after the first hyperthermia was assessed using a Wilcoxon Rank sum test as well as a paired T test.
With one exception, multivariate analysis was not attempted for correlation with treatment outcome because of the limited number of subjects. Bivariate and multivariate analysis performed between perfusion related parameters and other clinical variables as well as the pH parameters to determine whether these were related to each other. Corrections for multiple comparisons were not made.
Thirty-seven dogs (median age = 9.8 years, inter quartile range= 4.3 years) were evaluated with DCE-MRI before starting treatment. Seventeen of the dogs had a second DCE-MRI 24hr after the first thermoradiotherapy treatment. All subjects were planned to receive the second DCE-MRI study, but in 20 of these subjects, the data were either not obtained because of scheduling issues or because clean spectroscopic data could not be derived from the tissue for the second session which was required prior to the DCE-MRI per protocol design. The descriptive statistics of the sample characteristics are listed by thermal dose group in Table 1.
The population was balanced with respect to thermal dose group (low dose= 56.7%, and high dose= 43.3%). In the high thermal dose group, median temperature averaged T50 (median = 43.2°C; inter quartile range =1.9°C), T90 (median = 40.8°C; inter quartile range =0.7°C), CEM43°C T50 (median = 89.1 minutes; inter quartile range = 144.8 minutes) and CEM43°C T90 (median = 8.2 minutes; inter quartile range =6.4 minutes) and the total duration time of heating (median=214 minutes; inter quartile range=179.5 minutes). In the low thermal dose group, median temperature averaged T50 (median = 42.6°C; inter quartile range =1.7°C), T90 (median = 39.9°C; inter quartile range =0.6°C), CEM43°C T50 (median = 17.5 minutes; inter quartile range = 32.0 minutes) and CEM43°C T90 (median = 0.8 minutes; inter quartile range =0.6 minutes) and the total duration time of heating (median=103 minutes; inter quartile range=58 minutes).
The T50 and T90 values are descriptions of the frequency distribution of temperatures that are measured during treatment. The T50 is the median temperature and the T90 describes the temperature value that is exceeded by 90% of the measured values. This is sometimes referred to as the 10th percentile, but in the hyperthermia literature it has been traditionally referred to as the T90. CEM43° C is a conversion algorithm that converts any time-temperature history into an equivalent number of minutes at 43 °C. Details of this algorithm are published elsewhere.(19).
Cox proportional hazard ratio analyses demonstrated that several imaging-based parameters obtained prior to and after the first hyperthermia treatment were found to be significant in predicting metastasis free survival, time to local failure and overall survival along with total duration of heating (Table 2).
AUC t-max (median = 5.1; inter quartile range = 0.65) measured before therapy was predictive of time to local failure (p=0.02); Figure 3a). There was no significant correlation between AUC t-max and tumor volume or grade in bivariate analysis (Table 3). However, because of competing risks of animals developing distant disease before reaching an endpoint for local tumor control, caution needs to be considered with respect to how to interpret this result.
The median time to metastasis was 24 months and the 2 year overall survival rate was 0.36. This included animals that died and at necroscopy metastasis were found. Pre-treatment parameters that were found to be significant predictors of metastasis-free survival and overall survival included tumor grade (p<=0.01, 70%; intermediate/high=30%), volume (p<0.05, median 18.8 cm3; inter quartile range of 55.7 cm3) and washout (p<=0.02; median = 4.24; inter quartile range = 2.72, shown in Figure 3b). Better prognosis was associated with lower grade, smaller volume, and higher washout rate. The predictability of extracellular pH parameters (obtained using microelectrodes) from Lora-Michiels et. al. are shown for comparison, since these measurements were taken on the same subjects (Table 2). (14)
AUC t-max, AUC 60, AUC 90 and washin parameter (Figure 3C) obtained 24hr following the first hyperthermia treatment were also significantly correlated with outcome. In all cases, higher values were associated with improved prognosis. These data suggest that improvements in perfusion and perhaps oxygenation after hyperthermia treatment are a good prognostic sign.
Multivariate analysis demonstrated that pre treatment AUC t-max and washout were independent predictors of metastasis free survival and overall survival (p<0.05, Table 3). In contrast, bivariate analysis demonstrated that AUC t-max obtained post treatment was inversely related to tumor volume and tumor grade. Small and/or low-grade tumors had higher AUC t-max values (p<0.05; Table 3). Washout values and AUC values obtained after treatment also were negatively correlated with tumor volume in bivariate analysis (p<0.05; Table 3).
The total duration of hyperthermia was found to be prognostically important in our previous report. (3) In this subset analysis, duration of heating remained an independent predictor of metastasis free survival and overall survival with hazard ratios of 1.28 and 1.32 and p-values of 0.007 and 0.004, respectively (Table 2). In this current study, heating duration was correlated with tumor grade in a bivariate analysis (p<0.05; Table 3).
Relationships between the MRI parameters measured here with pH parameters reported in our previous paper(14) are shown in Table 4. Bivariate analysis demonstrated that post hyperthermia washout values were negatively correlated with pre-treatment intracellular pH (p<0.05; Table 4) and positively correlated with the difference posttreatment (post-pre) pHe (p<0.05; Table 4). Figure 3d depicts the relationship of post washout with the change of pHe demonstrating a positive relationship, consistent with the notion that improved perfusion after heating leads to more efficient clearance of acid from the tissue.
This study demonstrated that DCE-MRI- based parameters may be useful in predicting overall and metastasis free survival in canine patients with soft tissue sarcomas. The parameters from the signal enhancement curve allowed prediction of patient outcome regardless of being done prior to the first hyperthermia therapy or 24 hours after. To our knowledge, this is the first time that DCE-MRI parameters have been shown to be predictive of clinical outcome for patients with soft tissue sarcomas. However, the results are based on a small number of patients, so larger clinical trials with adequate statistical power are needed to verify this initial result.
For data acquired prior to treatment, AUC t-max emerged as being related to local tumor control. This parameter integrates signal over time for the tumor, truncating it when the signal reaches a maximum value in the reference muscle tissue. Consequently, this parameter probably relates to both perfusion and permeability. Tumors with higher AUC t-max might be better perfused and therefore better oxygenated. In bivariate analysis, this parameter was not associated with either tumor volume or grade, suggesting that it is an independent predictor of local tumor control (Table 3).
Higher washout values obtained prior to treatment were associated with greater metastasis-free and overall survival. This parameter relates to the reabsorption and clearance of contrast agent from the extravascular space. Thus, higher values maybe associated with a vasculature that is more efficient in transport. Factors that influence transport efficiency include vascular density, permeability and perfusion rate of the microvessels. (20–23).
In prior studies we demonstrated theoretically that adjustments in microvessel orientation can make quite dramatic differences in oxygen transport. (20, 21) The same principle should apply in reverse for an MR contrast agent. Thus, the combination of vascular density and orientation of microvessels are likely to contribute significantly to the differences in washout between different tumors.
Vascular permeability is related to the size of the solute, the concentration gradient across the microvessel wall and the physical characteristics of the vascular wall; due to the presence of large endothelial cell gaps and lack of basement membrane leading to increased permeability. (24, 25) For large solutes, such as proteins, transport is strongly governed by convection generated by the pressure gradient across the vascular wall. With the presence of elevated tumor interstitial fluid pressure, these gradients are negligible. (24, 25)
However, small molecules also undergo diffusive transport, so the influence of convection on the transport of a small molecule such as a chelated Gd contrast agent is negligible. Consequently, the Gd would likely be reabsorbed into the vasculature down its own concentration gradient once the kidneys clear the Gd from the general circulation. (24, 25)
It is difficult to know why animals with tumors with better transport characteristics would have longer metastasis-free and overall survival. It may be reflective of a more differentiated state, but washout was not significantly associated with either tumor size or grade, suggesting that it could be independently predictive of outcome (Table 3).Current studies by our group are investigating interrelationships between physiologic/metabolic and genomic parameters, as compared with DCE/MRI. From this we may decipher more insight into this observation.
It was surprising to find that DCE-MRI values obtained after the first hyperthermia treatment were also associated with outcome. Increases in AUC and washin after the first heat treatment were associated with prolonged metastasis free and overall survival (Table 3).This may relate back to the maturity of the vasculature. AUC t-max (along with other parameters) for the post treatment study were correlated with tumor volume and grade, suggesting that they may not be independent predictors of outcome. It is known that hyperthermia causes changes in permeability/perfusion but the distribution and amount may be dependent on the tumor volume/aggressiveness. Tumors with more mature vasculature may be able to respond more dynamically to thermal stress and therefore more readily increase perfusion in response to thermal stress. Presumably, tumors with more mature vasculature might be less likely to metastasize for a variety of reasons. They may be less hypoxic, which would tend to reduce upregulation of transcription factors that influence metastatic propensity, such as hypoxia inducible factor −1. (26).
Only a few studies have been published describing the prognostic properties of DCE-MRI for clinical efficacy; studies involving gliomas, head & neck, breast, lung and cervical cancers have been reported (Appendix Supplemental Table 1).However, to our knowledge, clinical studies involving prediction of outcome for soft-tissue sarcomas using DCE-MRI have not been reported.
AUCt-max was the only perfusion parameter to predict local failure in our study (Table 2).Similar results have been reported by Mayr et al. in patients with cervical carcinomas at early stages of radiation therapy using relative signal intensity parameters (Supplemental Table 1). (27, 28)
Two studies have evaluated DCE-MRI parameters after treatment. Decreased tumor perfusion, at the end of a course of fractionated radiotherapy assessed by signal intensity perfusion indexes (Initial slope, Tmax) was related to low rates of local recurrence in patients in head and neck cancer. (29) Decreased perfusion indexes using the two compartment model, Ktrans and Ve, had more than 65% tumor volume reduction after multimodality therapy in patients with breast cancer. (30) Similar to the head and neck trial these results are not surprising given they were obtained following therapy.
Although studies performed at the end of primary therapy are of interest scientifically, as they suggest that therapy eventually leads to reduction in perfusion, such information would have little impact on therapeutic choices. A more desirable approach is to predict likelihood of local control prior to/or during the early phases of treatment because such measurements could be used to alter the course of treatment and potentially lead to increased treatment efficacy.
Our results demonstrate that longer metastasis free survival and increased overall survival occurred in dogs with highly perfused tumors before hyperthermia treatment measured by increased washout rate and after treatment with increased washin rate, AUC: 60, 90 & t-max). Only one other study has been published that relates to these endpoints. An increased incidence of metastasis (and poorer survival) was observed in patients with Ewing’s sarcomas displaying high percentage of necrosis. (31) The percentage of necrosis was obtained by calculating non-enhanced tumor regions from pre and post contrast enhanced images. Although this study did not specifically use dynamic MR parameters, lack of contrast agent is due to a lack of delivery, i.e. perfusion.
Our patients were part of a large thermoradiotherapy clinical trial that tested effects of high vs. low thermal dose in dogs with spontaneous soft tissue sarcomas. (3) We reported that increased cumulative thermal dose was related to increased time to local failure. One potential mechanism underlying the improvement in local tumor control might be increased oxygenation, resulting from increased perfusion. We did not find an association between higher thermal dose and increased DCE-MRI parameters in this study, however. (Table 4).It may be that patient related parameters, such as the maturity of the vasculature or rates of tumor cell killing after the first thermoradiotherapy session had more of an influence on perfusion changes than thermal dose itself. Additionally, we did not measure changes in oxygenation of these tumors, so we cannot conclude whether the changes in DCE-MRI parameters were associated directly with improvements in tumor oxygenation. Studies of this type are ongoing now in our group.
Our prior analysis also showed that duration of heating time, independent of thermal dose, was related to metastasis free and overall survival. This recapitulates what we saw in the larger cohort of animals in this study. (3) A reasonable assumption might be that duration of heating would be related to perfusion in some way. For example the time required to reach the pre-determined thermal dose would be shorter for more poorly perfused tumors. In this subset analysis, we found that duration of heating was still important for overall and metastasis-free survival, but it was not related to any of the DCE/MRI parameters. There was a correlation between duration of heating and tumor grade. Higher grade tumors tended to take longer to adequately heat. This may have to do with a greater propensity for pre-existing necrosis in high grade tumors. Such tumors may develop power limiting hot spots in necrotic areas, which could lead to the need to prolong heating times to get the rest of the tumor exposed to the prescribed thermal dose.
Using the same animals in this study, we recently reported that low extracellular pH (pHe) is associated with increased likelihood for tumor metastasis and shortened overall survival. (14) The acidic environment within tumors is thought to exist because of metabolic aberrations leading to propensity for anaerobic metabolism (e.g. the Warburg effect) and/or induction of anaerobic metabolism as a result of hypoxia (e.g. the Pasteur effect). However, the degree of acidosis will also be influenced by how efficiently the lactate is removed from the tissue by perfusion. In this study there was no relationship between DCE-MRI parameters obtained prior to treatment and pH, but an increase in washout was associated with an increase in pH. This is consistent with washout being indicative of a more efficient vascular system for waste removal. The inverse relationship between intracellular pH and washout is more difficult to explain. Generally, intracellular pH is tightly regulated by a variety of proton pumps that move lactate and hydrogen ions out of the cell to maintain a neutral intracellular pH. (32) It is difficult to reconcile how intracellular pH could have any influence upon changes in DCE-MRI parameters after hyperthermia treatment. This may be a spurious observation.
There are two main models that have been used to derive physiologically-based parameters from dynamic images. The first is a two compartment model that includes the transfer coefficient between the intravascular and extravascular compartments (Ktrans), the extracellular volume fraction and vascular volume fraction. (33 , 34) The second model is an empirical fit of the signal enhancement data of a pixel or region of interest. An area under the curve (AUC) can be calculated with this empirical fit. AUC calculations and the fitted values of the empirical equation can then be used to evaluate the dynamic data and referenced to normal tissue, such as muscle. (17, 29, 35–38) This second technique has the advantage of not requiring an arterial input function (arterial concentration-time curve of the contrast agent) for analysis.
All of these methods attempt to ascertain the meaning of the dynamic signal from DCE-MRI into physiologically tangible properties, i.e. tumor perfusion and vascular permeability. Several prior reports have shown correlations between DCE-MRI parameters and treatment outcome. (27, 29, 31, 39–41)
In this study we used the second method, fitting the signal enhancement curve to an empirical equation. From this analysis, several DCE/MRI parameters were associated with treatment outcome in this study. In all cases, parameters that were associated with better overall perfusion indicated a better outcome. Being able to predict overall treatment outcome prior to, or shortly after treatment is initiated, potentially allows for treatment modification which may improve overall efficacy.
Although the protocol called for scans to be taken prior to and 24h after the first hyperthermia treatment, only 17 of the original 37 animals actually had data at this second time point. There were multiple reasons for lack of data, but the two main ones related to lack of good data fits on the second session or scheduling conflicts. The scans were obtained on a human scanner and there were times when we were unable to schedule the canine patients for the second scan. We might have been able to avoid the poor data fitting on the second scan, had we been able to analyze the results immediately after the scan was done. Unfortunately, this was not possible at the time that these studies were done. In fact, we did not know about the problem until years later, when the data were post analyzed. We have encountered similar problems previously in human (18) studies. This points to the need for more rapid evaluation of study related parameters, so that additional measurements could be made, thereby improving the data acquisition for studies that require multiple time points.
The canine sarcoma is an ideal model for human solid tumors in many respects. These advantages have been reviewed in detail, but are briefly summarized here. The natural history of canine sarcomas is very similar to that of humans (42). They are locally invasive and a proportion of them metastasize, making the achievement of local control challenging. For the purposes of hyperthermia studies, they are of the same size range as human tumors, making them amenable to heating, using the same heating technologies that are used in humans. There are many advantages of the canine tumor model in general. The patients are outbred and they are typically older and therefore have concomitant diseases like human patients do. They are immune competent, yet their tumors are only weakly antigenic, similar to humans (42). We have utilized this model extensively over the last 25 years.
Although the number of tumors imaged were limited, the results of this study suggest that DCE-MRI perfusion parameters are associated with various indicators of prognosis. Since delivery of nutrients (oxygen) and removal of waste (lactate) are dependent on perfusion, imbalances in delivery of nutrients and waste removal may contribute to aggressiveness of soft tissue sarcomas.
Summary of studies that used DCE-MRI to predict clinical outcome along with whether increases perfusion parameters were beneficial or punitive for survival.
Supported by a NIH Grant PO1CA42745 from the Department of Health and Human Services
This study demonstrates the ability to predict overall survival and metastasis free survival of canine patients with soft tissue sarcomas using MRI prior to and 24 hrs after the neoadjuvant hyperthermia/radiation therapy. In soft tissue sarcomas early metastasis is a common problem, requiring aggressive neo adjuvant, surgery, and adjuvant therapy in order to have a favorable outcome. The ability to use DCE-MRI to stratify these patients would have significant clinical impact in its subsequent potential to influence the aggressiveness of neo/adjuvant therapy along with determining if the therapy will be an effective treatment. To our knowledge this is the first study to demonstrate the use of DCE-MRI in soft tissue sarcomas and have an independent predictive ability on treatment efficacy.