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Optimal Decision Rules for Biomarker-Based Subgroup Selection for a Targeted Therapy in Oncology

机译:基于生物标志物的亚组选择用于肿瘤治疗的最佳决策规则

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摘要

Throughout recent years, there has been a rapidly increasing interest regarding the evaluation of so-called targeted therapies. These therapies are assumed to show a greater benefit in a pre-specified subgroup of patients—commonly identified by a predictive biomarker—as compared to the total patient population of interest. This situation has led to the necessity to develop biostatistical methods allowing an efficient evaluation of such treatments. Among others, adaptive enrichment designs have been proposed as a solution. These designs allow the selection of the most promising patient population based on an efficacy analysis at interim and restricting recruitment to these patients afterwards. As has recently been shown, the performance of the applied interim decision rule in such a design plays a crucial role in ensuring a successful trial. In this work, we investigate the situation when the primary outcome of the trial is a binary variable. Optimal decision rules are derived which incorporate the uncertainty about the treatment effects. These optimal decision rules are evaluated with respect to their performance in an adaptive enrichment design in terms of correct selection probability and power, and are compared to proposed ad hoc decision rules. Our methods are illustrated by means of a clinical trial example.
机译:近年来,人们对所谓的靶向疗法的评价迅速增长。假设这些治疗方法在预定义的患者亚组(通常由预测性生物标记物识别)中显示出比总患者群体更大的益处。这种情况导致有必要开发生物统计学方法,以有效评估此类治疗方法。其中,已经提出了自适应富集设计作为解决方案。这些设计允许根据中期疗效分析选择最有希望的患者人群,然后限制这些患者的招募。如最近所显示的,在这种设计中所应用的临时决策规则的性能在确保成功的审判中起着至关重要的作用。在这项工作中,我们调查了试验的主要结果是二进制变量的情况。得出了最佳决策规则,其中包含了有关治疗效果的不确定性。这些最佳决策规则根据正确的选择概率和能力在自适应浓缩设计中针对其性能进行评估,并与建议的临时决策规则进行比较。我们的方法通过一个临床试验实例进行说明。

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