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Two-stage randomization designs in drug development.

机译:药物开发中的两阶段随机设计。

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One challenge in oncology drug development is to determine whether a new agent to the care of patients should be added concurrently as a new component to standard of care (SOC) induction treatment, used sequentially as an extended maintenance treatment after SOC induction for patients responding to induction therapy, or used in both the induction and the maintenance settings. A two-stage randomization design (TSRD) addresses these questions simultaneously. In such trials patients are initially randomized to two induction therapies, followed by another randomization to maintenance therapy contingent upon disease remission under induction therapy. We survey recently proposed methods for analyzing time-to-event endpoints in TSRDs and discuss several issues related to the use of TSRDs including sample size calculation and multiplicity.An alternative drug development strategy is to perform several single randomization designs (SRDs) comparing induction and maintenance regimens, respectively. We present a simulation study, which compares TSRDs to several strategies based on SRDs in terms of total sample size and time to reach clinical decisions. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:肿瘤学药物开发中的一个挑战是确定是否应同时将护理患者的新药作为护理标准(SOC)诱导治疗的新组成部分,并在患者接受SOC诱导后依次用作扩展维持治疗感应疗法,或用于感应和维护设置中。两阶段随机设计(TSRD)同时解决了这些问题。在此类试验中,患者最初被随机分配到两种诱导疗法,然后根据诱导疗法下的疾病缓解情况,随机分配到维持治疗。我们调查了最近提出的用于分析TSRD中事件到达时间终点的方法,并讨论了与TSRD使用相关的几个问题,包括样本量计算和多重性。另一种药物开发策略是执行多个单个随机设计(SRD),比较诱导和维护方案,分别。我们提供了一项模拟研究,将TSRD与基于SRD的几种策略进行比较,以总样本量和达到临床决策的时间为依据。版权所有(c)2008 John Wiley&Sons,Ltd.

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