Bayer U.S. LLC Pharmaceuticals, Whippany, New Jersey, USA.
Pharm Stat. 2021 May;20(3):485-498. doi: 10.1002/pst.2089. Epub 2020 Dec 18.
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.
单臂一阶段或多阶段研究设计通常用于肿瘤学 II 期开发中,当主要关注的结果是肿瘤反应(二元变量)时。两种和三种结果设计都可用。Simon 两阶段设计是两种结果设计的一个著名例子。两结果试验的目的是拒绝零假设,即客观缓解率(ORR)小于或等于预定的低无趣率,或者拒绝替代假设,即 ORR 大于或等于某个目标率。Sargent 等人提出的三种结果设计允许有中间灰色决策区,既不拒绝这两个假设,也不拒绝这两个假设,以减少所需的研究规模。我们提出了新的基于贝叶斯后验概率的两结果和三结果设计,这些设计具有连续监测功能,符合频率规范,如 I 型和 II 型错误率。无效性和/或疗效边界基于置信函数,这可能需要更高水平的证据来进行早期和晚期停止,并且具有清晰和直观的解释。我们在这样的程序类中搜索最佳设计,这些设计在零假设下最小化给定的损失函数,例如平均样本大小。我们提出了几个例子,并将我们的设计与文献中的其他程序进行了比较,结果表明我们的设计具有良好的运行特性。