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A confidence function-based posterior probability design for phase II cancer trials

机译:基于置信功能的后型癌症试验后概率设计

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Single-arm one- or multi-stage study designs are commonly used in phase II oncology development when the primary outcome of interest is tumor response, a binary variable. Both two- and three-outcome designs are available. Simon two-stage design is a well-known example of two-outcome designs. The objective of a two-outcome trial is to reject either the null hypothesis that the objective response rate (ORR) is less than or equal to a pre-specified low uninteresting rate or to reject the alternative hypothesis that the ORR is greater than or equal to some target rate. Three-outcome designs proposed by Sargent et al. allow a middle gray decision zone which rejects neither hypothesis in order to reduce the required study size. We propose new two- and three-outcome designs with continual monitoring based on Bayesian posterior probability that meet frequentist specifications such as type I and II error rates. Futility and/or efficacy boundaries are based on confidence functions, which can require higher levels of evidence for early versus late stopping and have clear and intuitive interpretations. We search in a class of such procedures for optimal designs that minimize a given loss function such as average sample size under the null hypothesis. We present several examples and compare our design with other procedures in the literature and show that our design has good operating characteristics.
机译:单臂单阶段或多阶段研究设计通常用于II期肿瘤学发展,其主要结果是肿瘤反应,这是一个二元变量。两种和三种结果设计都可用。西蒙两阶段设计是两种结果设计的著名例子。双结果试验的目标是拒绝客观应答率(ORR)小于或等于预先指定的低无趣率的无效假设,或拒绝ORR大于或等于某个目标率的替代假设。Sargent等人提出的三种结果设计允许一个中间灰色决策区,该决策区拒绝两种假设,以减少所需的研究规模。我们提出了新的两个和三个结果设计,基于贝叶斯后验概率进行持续监测,满足频度规范,如I型和II型错误率。无效性和/或有效性界限基于信心函数,这可能需要更高水平的证据证明早期和晚期停止,并有清晰直观的解释。我们在一类这样的程序中搜索最优设计,以最小化给定的损失函数,例如在零假设下的平均样本量。我们给出了几个例子,并将我们的设计与文献中的其他程序进行了比较,表明我们的设计具有良好的操作特性。

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