PEACE V—Salvage Treatment of OligoRecurrent nodal prostate cancer Metastases (STORM): Acute Toxicity of a Randomized Phase 2 Trial

医学 不良事件通用术语标准 前列腺癌 雄激素剥夺疗法 随机对照试验 放射治疗 内科学 不利影响 毒性 临床终点 癌症 肿瘤科 外科
作者
Piet Ost,Shankar Siva,Sigmund Brabrand,Piet Dirix,Nick Liefhooghe,F. Otte,A. Gómez-Iturriaga,Wouter Everaerts,Mohamed Shelan,Antonio J. Conde-Moreno,F. López Campos,Alexandros Papachristofilou,Matthias Gückenberger,Marta Scorsetti,A. Zapatero,Ana-Elena Villafranca Iturre,C. Eíto,Felipe Couñago,Paolo Muto,Lien Van De Voorde,Nicolas Mach,Renée Bultijnck,Valérie Fonteyne,Daniel Moon,Kristian Thon,Carole Mercier,Vérane Achard,Karin Stellamans,Els Goetghebeur,Dries Reynders,Thomas Zilli
出处
期刊:European Urology Oncology [Elsevier]
被引量:4
标识
DOI:10.1016/j.euo.2023.09.007
摘要

Treatment recommendations for patients with limited nodal recurrences are lacking, and different locoregional treatment approaches are currently being used.The aim of this trial is to compare metastasis-directed therapy (MDT) with or without elective nodal pelvic radiotherapy (ENRT).PEACE V-Salvage Treatment of OligoRecurrent nodal prostate cancer Metastases (STORM) is an international, phase 2, open-label, randomized, superiority trial (ClinicalTrials.gov identifier: NCT03569241). Patients diagnosed with positron emission tomography-detected pelvic nodal oligorecurrence (five or fewer nodes) following radical local treatment for prostate cancer were randomized in a 1:1 ratio between arm A (MDT and 6 mo of androgen deprivation therapy [ADT]) and arm B (ENRT [25 × 1.8 Gy] with MDT and 6 mo of ADT).We report the secondary endpoint acute toxicity, defined as worst grade ≥2 Common Terminology Criteria for Adverse Events v4.0 gastrointestinal (GI) or genitourinary (GU) toxicity within 3 mo of treatment. The chi-square test was used to compare toxicity between treatment arms. We also compare the quality of life (QoL) using the European Organisation for Research and Treatment of Cancer QLQ C30 and PR25 questionnaires.Between June 2018 and April 2021, 196 patients were assigned randomly to MDT or ENRT. Ninety-seven of 99 patients allocated to MDT and 93 of 97 allocated to ENRT received per-protocol treatment. Worst acute GI toxicity proportions were as follows: grade ≥2 events in three (3%) in the MDT group versus four (4%) in the ENRT group (p = 0.11). Worst acute GU toxicity proportions were as follows: grade ≥2 events in eight (8%) in the MDT group versus 12 (13%) in the ENRT group (p = 0.95). We observed no significant difference between the study groups in the proportion of patients with a clinically significant QoL reduction from baseline for any subdomain score area.No clinically meaningful differences were observed in worst grade ≥2 acute GI or GU toxicity or in QoL subdomains between MDT and ENRT.We found no evidence of differential acute bowel or urinary side effects using metastasis-directed therapy and elective nodal radiotherapy for the treatment of patients with a pelvic lymph node recurrence.
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