A randomized study of consolidation chemo-radiotherapy versus observation after first-line chemotherapy in advanced gall bladder cancers (RACE-GB Study): trial protocol

S. Agrawal, Ashish Singh, Rahul, P. Mishra, R. Saxena
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Abstract

Background: Chemotherapy (CT) is the standard of care for advanced gall bladder cancer (GBC). However, after completion of 6 cycles of CT, a proportion of patients with good performance status progress within a few months. Retrospective data in locally advanced cases revealed that consolidation chemo-radiotherapy (CTRT) in responders to CT and with good performance status improves overall survival. Methods: FNA proven advanced GBC with predefined clinical-radiological features will be administered 4 cycles CT (cisplatin-gemcitabine combination). After completion of CT, those in good Karnofsky performance status (KPS) will be randomised to consolidation CTRT versus observation (standard of care). The primary end point of the study is to compare OS between the two arms. The secondary end point is to compare progression free survival (PFS), toxicity, and quality of life between the two study arms. The trial is designed to detect an improvement in 2-year overall survival (OS) from 8% in the control arm to 25% in study arm with 80.0% power at a 0.05 significance level. The resultant sample size to achieve this aim is 140 (70 in each arm) over a duration of 4-5 years with a 10% attrition rate. Accrual has been from January 2019 to October 2022. Conclusions: This trial aims to assess the incremental gain in outcomes with consolidation CTRT versus observation in responders to first-line CT in advanced GBCs. This is the first randomised study to evaluate role of consolidation chemoradiation. Trial Registration: The trial is registered with clinical trials registry India (CTRI/2019/04/025204) and clinical trials.gov (NCT05493956).
晚期胆囊癌巩固化疗与一线化疗后观察的随机研究(RACE-GB研究):试验方案
背景:化疗(CT)是晚期胆囊癌(GBC)的标准治疗方法。然而,在完成6个周期CT后,有一部分表现良好的患者在几个月内病情有所好转。局部晚期病例的回顾性数据显示,对CT有反应且表现良好的患者进行巩固化疗(CTRT)可提高总生存率。方法:经证实具有预定临床放射学特征的晚期GBC患者将接受4周期CT治疗(顺铂-吉西他滨联合)。CT完成后,Karnofsky表现状态(KPS)良好的患者将随机分为巩固CTRT组和观察组(标准护理组)。研究的主要终点是比较两组的OS。次要终点是比较两个研究组的无进展生存期(PFS)、毒性和生活质量。该试验旨在检测2年总生存率(OS)从对照组的8%提高到研究组的25%,功率为80.0%,显著性水平为0.05。达到这一目标的最终样本量为140例(每组70例),持续4-5年,损耗率为10%。应计时间为2019年1月至2022年10月。结论:本试验旨在评估巩固性CTRT与观察性一线CT对晚期GBCs的疗效的增量增益。这是第一个评估巩固放化疗作用的随机研究。试验注册:该试验已在印度临床试验注册中心(CTRI/2019/04/025204)和clinical trials.gov (NCT05493956)注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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