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The role of the expansion cohort in phase I trials in oncology: Guidelines of the phase I HUB

机译:扩展队列在肿瘤学I期试验中的作用:HUB期指南

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摘要

At the end of the dose escalation step of phase I trials in oncology, it is increasingly frequent to include patients in expansion cohorts. However, the objective of the expansion cohorts, the number of patients included and their justification are insufficiently explained in the protocols. These cohorts are sometimes of considerable size. The aim of this article is to outline the methodology of expansion cohorts in order to provide recommendations for their planning in practice. This work has been undertaken in collaboration with the statisticians of the early phase investigation centers (CLIP2), supported by INCA. First, we have outlihed the recent articles published on the expansion cohorts in phase I. We then proposed recommendations, in terms of objectives and number of patients to be included, to guide investigators and facilitate the use of these expansion cohorts in practice. Manji et al. have identified 149 phase I clinical trials using expansion cohorts in oncology with a review of the literature between 2006 and 2011 (Manji et al., 2013). Objectives of the expansion cohort were reported in 111 trials (74%). In these trials, safety was the most reported objective (80% of trials), followed by efficacy (45%). According to this review, the number of patients included in these cohorts was insufficiently justified. This result was confirmed by the study of literature that we conducted over the period 2011-2014. We propose to define the number of patients to be included in expansion cohorts in terms of (1) their objectives, (2) the statistical criteria and (3) the clinical context of the trial. The toxicity study remains the primary objective to evaluate in the expansion phase. In some contexts, the activity study is considered as co-primary objective, either for identifying preliminary signs of activity in studies like screening, or for studying the activity when the target population is known. This study is then considered as phase I/II, and experience plans of phase II can be adapted for planning expansion cohorts. Recommendations for the size of expansion cohorts are proposed. Despite the exploratory character of the expansion cohort, a justification of their size based on assumptions statistically defined is recommended in order to provide an interpretable conclusion and to quantify the risk of errors.
机译:在肿瘤学I期试验的剂量递增步骤结束时,越来越多的患者被纳入扩展队列。但是,方案中并未充分说明扩展队列的目的,纳入的患者人数及其合理性。这些队列有时规模很大。本文的目的是概述扩展群组的方法,以便为他们的实践规划提供建议。在INCA的支持下,这项工作是与早期调查中心(CLIP2)的统计人员合作完成的。首先,我们没有刊登关于第一阶段扩展队列的最新文章。然后,我们针对目标和要纳入的患者数量提出了建议,以指导研究人员并促进在实践中使用这些扩展队列。 Manji等。已有149项I期临床试验使用肿瘤扩展队列研究,并回顾了2006年至2011年之间的文献(Manji等,2013)。在111个试验中报告了扩展队列的目标(74%)。在这些试验中,安全性是报告最多的目标(试验的80%),其次是疗效(45%)。根据该评价,这些队列中包括的患者数量不足以证明其合理性。我们在2011-2014年期间进行的文献研究证实了这一结果。我们建议根据(1)他们的目标,(2)统计标准和(3)试验的临床背景来定义纳入扩展队列的患者数量。毒性研究仍然是在扩展阶段进行评估的主要目标。在某些情况下,活动研究被视为共同首要目标,或者用于确定诸如筛选等研究活动的初步迹象,或者用于在目标人群已知时研究活动。然后,该研究被视为I / II阶段,并且II阶段的经验计划可以用于计划扩展队列。提出了有关扩展队列规模的建议。尽管扩展队列具有探索性,但仍建议根据统计定义的假设对它们的大小进行合理化,以便提供可解释的结论并量化错误风险。

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