Abstract

Background and purposeTreatment of intermediate and high-risk prostate cancer with a high BED has been shown to increase recurrence free survival (RFS). While high dose rate (HDR) brachytherapy, given as a boost is effective in delivering a high BED, many patients are not candidates for the procedure or wish to avoid an invasive procedure. We evaluated the use of stereotactic body radiotherapy (SBRT) as a boost, with dosimetry modeled after HDR-boost.Material and methodsFifty patients were treated with two fractions of SBRT (9.5-10.5 Gy/fraction) after 45 Gy external-beam radiotherapy, with 48 eligible for analysis at a median follow-up of 42.7 months.ResultsThe Kaplan-Meier estimates of biochemical control post-radiation therapy (95 % Confidence Interval) at 3, 4 and 5 years were 95 % (81–99 %), 90 % (72–97 %) and 90 % (72–97 %), respectively (not counting 2 patients with a PSA bounce as failures). RFS (defined as disease recurrence or death) estimates at 3, 4 and 5 years were 92 % (77–97 %), 88 % (69–95 %) and 83 % (62–93 %) if patients with PSA bounces are not counted as failures, and were 90 % (75–96 %), 85 % (67–94 %) and 75 % (53–88 %) if they were. The median time to PSA nadir was 26.2 months (range 5.8–82.9 months), with a median PSA nadir of 0.05 ng/mL (range <0.01–1.99 ng/mL). 2 patients had a “benign PSA bounce”, and 4 patients recurred with radiographic evidence of recurrence beyond the RT fields. Treatment was well tolerated with no acute G3 or higher GI or GU toxicity and only a single G3 late GU toxicity of urinary obstruction.ConclusionsSBRT boost is well-tolerated for intermediate and high-risk prostate cancer patients with good biochemical outcomes and low toxicity.

Highlights

  • Patients with intermediate and high-risk prostate cancer have poorer clinical outcomes than patients with lowrisk prostate cancer, and in need of more intensified therapeutic options

  • recurrence free survival (RFS) estimates at 3, 4 and 5 years were 92 % (77– 97 %), 88 % (69–95 %) and 83 % (62–93 %) if patients with PSA bounces are not counted as failures, and were 90 % (75–96 %), 85 % (67–94 %) and 75 % (53–88 %) if they were

  • This study differs from previous studies in that we present the results of stereotactic body radiotherapy (SBRT) as a boost after CF-External beam radiotherapy (EBRT) in a higher risk group of patients and discuss PSA kinetics, biochemical control, toxicity and patterns of recurrence

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Summary

Introduction

Patients with intermediate and high-risk prostate cancer have poorer clinical outcomes than patients with lowrisk prostate cancer, and in need of more intensified therapeutic options. Our goal was to develop and demonstrate a non-invasive method of delivering a dose and fractionation equivalent to an HDR boost using stereotactic body radiotherapy (SBRT) for patients with intermediate and high-risk prostate cancer. Our hypothesis was that the SBRT delivered in 2 fractions of 9.5 to 10.5 Gy should result in equivalent biochemical control and toxicity profile as HDR without the need for an invasive, operative procedure. This study differs from previous studies in that we present the results of SBRT as a boost after CF-EBRT in a higher risk group of patients and discuss PSA kinetics, biochemical control, toxicity and patterns of recurrence. Treatment of intermediate and high-risk prostate cancer with a high BED has been shown to increase recurrence free survival (RFS). We evaluated the use of stereotactic body radiotherapy (SBRT) as a boost, with dosimetry modeled after HDR-boost

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