Biostatistics and Programming, Sanofi, Bridgewater, New Jersey.
Pharm Stat. 2020 Jul;19(4):468-481. doi: 10.1002/pst.1985. Epub 2020 Jan 6.
Decision making is a critical component of a new drug development process. Based on results from an early clinical trial such as a proof of concept trial, the sponsor can decide whether to continue, stop, or defer the development of the drug. To simplify and harmonize the decision-making process, decision criteria have been proposed in the literature. One of them is to exam the location of a confidence bar relative to the target value and lower reference value of the treatment effect. In this research, we modify an existing approach by moving some of the "stop" decision to "consider" decision so that the chance of directly terminating the development of a potentially valuable drug can be reduced. As Bayesian analysis has certain flexibilities and can borrow historical information through an inferential prior, we apply the Bayesian analysis to the trial planning and decision making. Via a design prior, we can also calculate the probabilities of various decision outcomes in relationship with the sample size and the other parameters to help the study design. An example and a series of computations are used to illustrate the applications, assess the operating characteristics, and compare the performances of different approaches.
决策是新药开发过程中的一个关键组成部分。基于早期临床试验(如概念验证试验)的结果,赞助商可以决定是继续、停止还是推迟药物的开发。为了简化和协调决策过程,文献中提出了决策标准。其中之一是检查置信区间的位置相对于治疗效果的目标值和下限参考值。在这项研究中,我们通过将一些“停止”决策转移到“考虑”决策来修改现有的方法,以减少直接终止有潜在价值药物开发的可能性。由于贝叶斯分析具有一定的灵活性,可以通过推理先验来借用历史信息,因此我们将贝叶斯分析应用于试验设计和决策中。通过设计先验,我们还可以计算出与样本量和其他参数相关的各种决策结果的概率,以帮助研究设计。通过一个示例和一系列计算来说明应用、评估操作特性,并比较不同方法的性能。