scholarly journals Simulation of an HDR “Boost” with Stereotactic Proton versus Photon Therapy in Prostate Cancer: A Dosimetric Feasibility Study

Author(s):  
Jill S. Remick ◽  
Pouya Sabouri ◽  
Mingyao Zhu ◽  
Søren M. Bentzen ◽  
Kai Sun ◽  
...  

Abstract Purpose/Objectives To compare the dose escalation potential of stereotactic body proton therapy (SBPT) versus stereotactic body photon therapy (SBXT) using high-dose rate prostate brachytherapy (HDR-B) dose-prescription metrics. Patients and Methods Twenty-five patients previously treated with radiation for prostate cancer were identified and stratified by prostate size (≤ 50cc; n = 13, > 50cc; n = 12). Initial CT simulation scans were re-planned using SBXT and SBPT modalities using a prescription dose of 19Gy in 2 fractions. Target coverage goals were designed to mimic the dose distributions of HDR-B and maximized to the upper limit constraint for the rectum and urethra. Dosimetric parameters between SBPT and SBXT were compared using the signed-rank test and again after stratification for prostate size (≤ 50cm3 and >50cm3) using the Wilcoxon rank test. Results Prostate volume receiving 100% of the dose (V100) was significantly greater for SBXT (99%) versus SBPT (96%) (P ≤ 0.01), whereas the median V125 (82% vs. 73%, P < 0.01) and V200 (12% vs. 2%, P < 0.01) was significantly greater for SBPT compared to SBXT. Median V150 was 49% for both cohorts (P = 0.92). V125 and V200 were significantly correlated with prostate size. For prostates > 50cm3, V200 was significantly greater with SBPT compared to SBXT (14.5% vs. 1%, P = 0.005), but not for prostates 50cm3 (9% vs 4%, P = 0.11). Median dose to 2cm3 of the bladder neck was significantly lower with SBPT versus SBXT (9.6 Gy vs. 14 Gy, P < 0.01). Conclusion SBPT and SBXT can be used to simulate an HDR-B boost for locally advanced prostate cancer. SBPT demonstrated greater dose escalation potential than SBXT. These results are relevant for future trial design, particularly in patients with high risk prostate cancer who are not amenable to brachytherapy.

2014 ◽  
Vol 32 (4_suppl) ◽  
pp. 106-106
Author(s):  
Juanita M. Crook ◽  
Ana Ots ◽  
Brent Parker ◽  
Matt Schmid ◽  
Deidre Batchelar ◽  
...  

106 Background: To demonstrate feasibility of using high dose rate (HDR) brachytherapy to deliver 25% higher than prescription dose to the dominant intra-prostatic lesion (DIL) as defined on multi-parametric MRI for intermediate and high risk prostate cancer. Methods: Twenty six patients with predominantly unilateral disease consented to a University Ethics-approved phase II study of selective dose escalation. HDR brachytherapy was performed in weeks 1 and 3 of treatment, each delivering one fraction of 10 Gy to the whole prostate. External beam consisted of 46Gy/23 fractions starting 3 days after the first HDR fraction.T2 FSE images were obtained using 1.5T endorectal MRI in transverse, sagittal and coronal planes followed by Dynamic Contrast Enhancement after injection of gadolinium. Apparent Diffusion Coefficient maps were calculated. The DIL was contoured on the MRI and, following image registration, transposed to the preoperative TRUS performed in the treatment position. Intra-operative TRUS with source-delivery catheters in place was fused to the pre-op TRUS with the transposed DIL. The DIL was included in dose optimization criteria. Results: Twenty five of 26 patients had a visible DIL. Mean prostate percentage receiving the prescription dose (V100) was 98.2% (SD:1.1). Mean dose to 90% of the DIL (D90) was 13.2 Gy (SD: 1.7). DIL mean volume was 2.9 cc (SD:1.8) representing 9.5% (SD: 7.6) of the prostate volume. Coverage of the DIL was excellent with a median of 97% receiving the planned escalation of 25%. Established dose constraints to rectum and urethra were respected in all cases. The factor that limited DIL coverage was proximity to organs at risk. Peri-urethral location of the DIL limited coverage in five cases and two had a posterior DIL such that dose to the rectum limited escalation. However, these seven cases still achieved a mean DIL D90 of 12.2 Gy. Conclusions: Dose manipulation using US-planned HDR brachytherapy is readily achievable within the practice setting of a community cancer center. Dose escalation to the DIL to a mean of 132% of the prescribed dose for selected intermediate and high risk prostate cancer patients is feasible while respecting critical organ constraints. Further escalation is planned. Clinical trial information: NCT01605097.


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