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骨盆或受累淋巴结治疗:前列腺癌复发的根除(POINTER-PC)——一项III期多中心、开放标签随机对照试验的研究方案论文

Pelvis Or Involved Node Treatment: Eradicating Recurrence in Prostate Cancer (POINTER-PC) - study protocol paper for a phase III multicentre, open-label randomised controlled trial.

作者信息

Slevin Finbar, Alexander Sophie, Brown Sarah R, Carter Matthew, Choudhury Ananya, Clipson Alexandra, Din Omar, Dive Caroline, Gilbert Alexandra, Girvan Sean, Hingorani Mohan, Jain Suneil, Khoo Vincent, Lilley John, Murray Louise J, Naismith Olivia, Noutch Samantha, Oliveira Pedro, Pagett Christopher J H, Smith Alexandra, Talbot James, Webster Joanne, Henry Ann M

机构信息

Leeds Institute of Medical Research, University of Leeds, Leeds, UK

Leeds Teaching Hospitals NHS Trust, Leeds, UK.

出版信息

BMJ Open. 2024 Dec 26;14(12):e095560. doi: 10.1136/bmjopen-2024-095560.

Abstract

INTRODUCTION

Prostate cancer (PCa) is the most common cancer in men. Recurrence may occur in up to half of patients initially treated with curative intent for high-risk localised/locally advanced PCa. Pelvic nodal recurrence is common in this setting, but no clear standard of care exists for these patients, with potential therapeutic approaches including stereotactic body radiotherapy (SBRT) to the involved node(s) alone, extended nodal irradiation (ENI) to treat sites of potential micrometastatic spread in addition to involved node(s) and androgen deprivation therapy with or without additional systemic anticancer therapies. Based on observational studies, ENI is associated with promising metastasis-free survival (MFS) compared with SBRT and appears to result in low rates of severe late toxicity.

METHODS AND ANALYSIS

Pelvis Or Involved Node Treatment: Eradicating Recurrence in Prostate Cancer is a UK multicentre, open-label, phase III randomised controlled trial, which will deliver much needed, high-quality evidence of the impact on metastatic progression from ENI compared with SBRT in patients with PCa pelvic nodal recurrence. The trial will also evaluate the long-term toxicity of 5-fraction ENI compared with a standard 20-fraction schedule. The trail will randomise 480 participants in a ratio of 2:1:1 to SBRT, 5-fraction ENI or 20-fraction ENI from 35 to 40 UK radiotherapy sites over 4 years. Coprimary endpoints are MFS at 3 years and participant-reported late bowel toxicity at 3 years. Secondary endpoints include overall survival, biochemical progression-free survival, failure-free survival, patterns of failure, participant-reported/clinician-reported toxicity and health-related quality of life. Collection of blood and tissue samples will enable future evaluation of biomarkers of disease and toxicity and support stratification of salvage therapeutic approaches.

ETHICS AND DISSEMINATION

Ethical approval was obtained from NHS Health Research Authority, East of England - Cambridgeshire and Hertfordshire Research Ethics Committee (24/EE/0099). Trial results will be published in peer-reviewed journals and adhere to International Committee of Medical Journal Editors guidelines.

TRIAL REGISTRATION NUMBER

ISRCTN11089334, registered on 23 September 2024.

摘要

引言

前列腺癌(PCa)是男性中最常见的癌症。对于最初接受根治性治疗的高危局限性/局部晚期PCa患者,高达一半可能会出现复发。盆腔淋巴结复发在这种情况下很常见,但对于这些患者尚无明确的标准治疗方案,潜在的治疗方法包括单独对受累淋巴结进行立体定向体部放疗(SBRT)、除受累淋巴结外对潜在微转移扩散部位进行扩大野淋巴结照射(ENI)以及联合或不联合其他全身抗癌治疗的雄激素剥夺治疗。基于观察性研究,与SBRT相比,ENI与有前景的无转移生存期(MFS)相关,并且似乎导致严重晚期毒性发生率较低。

方法与分析

骨盆或受累淋巴结治疗:根除前列腺癌复发是一项英国多中心、开放标签、III期随机对照试验,该试验将提供急需的高质量证据,证明与SBRT相比,ENI对PCa盆腔淋巴结复发患者转移进展的影响。该试验还将评估5次分割的ENI与标准的20次分割方案相比的长期毒性。该试验将在4年内从英国35至40个放疗地点以2:1:1的比例将480名参与者随机分配至SBRT、5次分割的ENI或20次分割的ENI组。共同主要终点是3年时的MFS和参与者报告的3年时的晚期肠道毒性。次要终点包括总生存期、无生化进展生存期、无失败生存期、失败模式、参与者报告/临床医生报告的毒性以及健康相关生活质量。血液和组织样本的收集将有助于未来评估疾病和毒性的生物标志物,并支持挽救性治疗方法的分层。

伦理与传播

已获得英国国民健康服务体系健康研究管理局、英格兰东部 - 剑桥郡和赫特福德郡研究伦理委员会(24/EE/0099)的伦理批准。试验结果将发表在同行评审期刊上,并遵循国际医学期刊编辑委员会的指南。

试验注册号

ISRCTN11089334,于2024年9月23日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ff/11683931/805be422e8cc/bmjopen-14-12-g001.jpg

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