使用信息共轭先验的II期临床试验贝叶斯样本量计算

Matthew S. Mayo , Byron J. Gajewski
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引用次数: 43

摘要

许多研究人员从贝叶斯的角度讨论了II期临床试验。Tan和Machin最近的一篇文章侧重于样本量的计算,他们通过指定弥漫性先验分布,然后计算真实响应将超过预定目标的后验概率来确定样本量。在本文中,我们扩展了这些样本量计算,包括使用各种策略的信息先验分布,这些策略允许具有乐观和悲观先验的研究人员直接参与样本量决策。我们通过多种方法选择信息先验,这些方法由共轭先验的均值、中值或模式决定。这些情况可能导致不同的样本量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bayesian sample size calculations in phase II clinical trials using informative conjugate priors

A number of researchers have discussed phase II clinical trials from a Bayesian perspective. A recent article by Tan and Machin focuses on sample size calculations, which they determine by specifying a diffuse prior distribution and then calculating a posterior probability that the true response will exceed a prespecified target. In this article, we extend these sample size calculations to include informative prior distributions using various strategies that allow researchers with both optimistic and pessimistic priors direct involvement in the sample size decision making. We select the informative priors via multiple methods determined by the mean, median or mode of the conjugate prior. These cases can result in varying sample sizes.

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