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Helical intensity-modulated Radiotherapy of the Pelvic Lymph Nodes with Integrated Boost to the Prostate Bed - Initial Results of the PLATIN 3 Trial

机译:盆腔淋巴结螺旋增强调制放射疗法与前列腺床的综合加强疗法-PLATIN 3试验的初步结果

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Background 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. Methods From 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. Results Of 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. Conclusions Postoperative whole-pelvis IMRT with an integrated boost to the prostate bed can be performed safely and without excessive toxicity. Trial registration Trial Numbers: ARO 2009–05, ClinicalTrials.gov: NCT01903408 .
机译:背景技术前列腺床的辅助和抢救放疗是前列腺癌的既定治疗选择。虽然对骨盆淋巴结进行额外放疗的益处仍存在争议,但PLATIN 3前瞻性II期临床试验已启动,以证实骨盆淋巴结和前列腺床术后IMRT的毒性数据。方法2009年至2011年,对40例前列腺癌术后高危前列腺癌患者进行pT3 R0 / 1?M0或pT2 R1 M0或PSA复发,淋巴结受累和不充分的淋巴结清扫术或pN?+≥20%的风险。被注册。患者在放疗前接受了两个月的抗激素治疗(AT)。在放疗期间必须继续进行AT,建议再延长两年。以34个分数同时进行盆腔淋巴结(51.0?Gy)的IMRT和对前列腺床的同时整合增强(68.0?Gy)。定期评估PSA水平,前列腺相关症状和生活质量,持续24个月。结果在40名患者中,有39名按计划完成了治疗。总体急性毒性发生率低,没有发生3/4级急性毒性。只有22.5%的患者经历过急性2级胃肠道(GI)和泌尿生殖道(GU)毒性。在随访期间,发生了10.0%的2级晚期GI和5.0%的2UG晚期毒性,一名患者发生了3级晚期直肠炎和肠炎。经过24个月的中位观察时间后,PLATIN 3试验已在所有患者中97.5%显示了足够的安全性,因此达到了其预期的目标。中位数24个月后,有34/38例患者没有PSA复发。结论可以安全地进行术后全骨盆IMRT,并能对前列腺床进行整体增强,且无过度毒性。试验注册试验编号:ARO 2009-05,ClinicalTrials.gov:NCT01903408。

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