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A randomized two-stage design for phase II clinical trials based on a Bayesian predictive approach

机译:基于贝叶斯预测方法的II期临床试验的随机两阶段设计

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摘要

The rate of failure in phase III oncology trials is surprisingly high, partly owing to inadequate phase II studies. Recently, the use of randomized designs in phase II is being increasingly recommended, to avoid the limits of studies that use a historical control. We propose a two-arm two-stage design based on a Bayesian predictive approach. The idea is to ensure a large probability, expressed in terms of the prior predictive probability of the data, of obtaining a substantial posterior evidence in favour of the experimental treatment, under the assumption that it is actually more effective than the standard agent. This design is a randomized version of the two-stage design that has been proposed for single-arm phase II trials by Sambucini. We examine the main features of our novel design as all the parameters involved vary and compare our approach with Jung's minimax and optimal designs. An illustrative example is also provided online as a supplementary material to this article. Copyright (C) 2014 John Wiley & Sons, Ltd.
机译:III期肿瘤学试验的失败率非常高,部分原因是II期研究不足。最近,越来越多地建议在第二阶段使用随机设计,以避免使用历史对照的研究的局限性。我们提出一种基于贝叶斯预测方法的两臂两阶段设计。这样做的想法是确保以很大的概率(根据数据的先验预测概率来表示)获得大量后验证据以支持实验治疗,前提是它实际上比标准药物更有效。该设计是Sambucini提出用于单臂II期临床试验的两阶段设计的随机版本。由于涉及的所有参数均发生变化,因此我们研究了新颖设计的主要特征,并将我们的方法与Jung的minimax和最优设计进行了比较。在线提供了一个示例性示例作为本文的补充材料。版权所有(C)2014 John Wiley&Sons,Ltd.

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