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一种新的分层自适应 II 期设计如何改善目标人群。

How a new stratified adaptive phase II design could improve targeting population.

机构信息

Centre d'Investigation Clinique P-0802, CHU Poitiers, France.

出版信息

Stat Med. 2011 Jun 15;30(13):1555-62. doi: 10.1002/sim.4211. Epub 2011 Mar 22.

Abstract

Phase II clinical trials in oncology are used for initial evaluation of the therapeutic efficacy of a new treatment regimen. Simon's two-stage or Fleming designs are commonly used for such trials. Treatment effect dilution may be observed because of heterogeneity of the population leading to negative conclusion on the whole population and termination of drug development while patients with particular characteristics may have benefit. Several authors have proposed alternative strategies based on Simon's design, including stratification on the patients' characteristics. In this paper, the authors develop a new stratified phase II design, allowing early stop of the trial for efficacy as it is an extension of Fleming's design. An example based on real data is given and the results from exact binomial calculations are developed to explore several assumptions on response rates, prevalence of each population and errors.

摘要

肿瘤学的 II 期临床试验用于初步评估新治疗方案的治疗效果。西蒙的两阶段或弗莱明设计常用于此类试验。由于人群的异质性,可能会观察到治疗效果稀释,从而导致对整个人群的负面结论,并终止药物开发,而具有特定特征的患者可能会受益。一些作者已经提出了基于西蒙设计的替代策略,包括根据患者特征进行分层。在本文中,作者开发了一种新的分层 II 期设计,允许根据疗效提前停止试验,因为它是弗莱明设计的扩展。给出了一个基于真实数据的示例,并通过精确二项式计算得出了结果,以探讨对反应率、每个人群的患病率和误差的几种假设。

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