Abstract

BackgroundAdjuvant and salvage radiotherapy of the prostate bed are established treatment options for prostate cancer. While the benefit of an additional radiotherapy of the pelvic lymph nodes is still under debate, the PLATIN 3 prospective phase II clinical trial was initiated to substantiate toxicity data on postoperative IMRT of the pelvic lymph nodes and the prostate bed.MethodsFrom 2009 to 2011, 40 patients with high-risk prostate cancer after prostatectomy with pT3 R0/1 M0 or pT2 R1 M0 or a PSA recurrence and either > 20% risk of lymph node involvement and inadequate lymphadenectomy or pN + were enrolled. Patients received two months of antihormonal treatment (AT) before radiotherapy. AT continuation was mandatory during radiotherapy and was recommended for another two years. IMRT of the pelvic lymph nodes (51.0 Gy) with a simultaneous integrated boost to the prostate bed (68.0 Gy) was performed in 34 fractions. PSA level, prostate-related symptoms and quality of life were assessed at regular intervals for 24 months.ResultsOf the 40 patients enrolled, 39 finished treatment as planned. Overall acute toxicity rates were low and no acute grade 3/4 toxicity occurred. Only 22.5% of patients experienced acute grade 2 gastrointestinal (GI) and genitourinary (GU) toxicity. During follow-up, 10.0% late grade 2 GI and 5.0% late grade 2 GU toxicity occurred, and one patient developed late grade 3 proctitis and enteritis. After a median observation time of 24 months the PLATIN 3 trial has shown in 97.5% of all patients sufficient safety and thus met its prospectively defined aims. After a median of 24 months, 34/38 patients were free of a PSA recurrence.ConclusionsPostoperative whole-pelvis IMRT with an integrated boost to the prostate bed can be performed safely and without excessive toxicity.Trial registrationTrial Numbers: ARO 2009–05, ClinicalTrials.gov: NCT01903408.

Highlights

  • Adjuvant and salvage radiotherapy of the prostate bed are established treatment options for prostate cancer

  • A benefit could only be shown for high risk patients (5 year biochemical recurrence free survival (BFS) 47% vs. 21%, for WPRT vs. PBRT, respectively)

  • Briganti et al showed in a matched-pair analysis of 703 pT2-4 pN + patients that the combination of androgen deprivation and radiotherapy prolonged cause-specific and overall survival compared to androgen deprivation alone [7]

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Summary

Introduction

Adjuvant and salvage radiotherapy of the prostate bed are established treatment options for prostate cancer. While the benefit of an additional radiotherapy of the pelvic lymph nodes is still under debate, the PLATIN 3 prospective phase II clinical trial was initiated to substantiate toxicity data on postoperative IMRT of the pelvic lymph nodes and the prostate bed. Postoperative radiotherapy of the prostate bed (PBRT) is a standard procedure for patients with an increased risk of local recurrence. Three prospective randomised trials demonstrated that PBRT significantly increases the biochemical recurrence free survival (BFS) compared to observation: EORTC 22911 [1], SWOG 8794 [2] and ARO 96–02 [3]. A benefit could only be shown for high risk patients (5 year BFS 47% vs 21%, for WPRT vs PBRT, respectively). A retrospective cohort study of 247 patients comparing WPRT vs. PBRT that excluded patients under androgen suppression only demonstrated a benefit regarding biochemical control for patients with a pretreatment PSA ≥ 0.4 ng/ml [8]

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