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基于计数数据终点和连续终点的中期结果无效性标准进行试验监测。

Trial monitoring via a futility criterion for interim results on a count data endpoint and a continuous endpoint.

机构信息

Biostatistics and Programming, Sanofi, 55 Corporate Drive, Bridgewater, NJ 08807, United States of America.

Biostatistics and Programming, Sanofi, 55 Corporate Drive, Bridgewater, NJ 08807, United States of America.

出版信息

Contemp Clin Trials. 2021 Apr;103:106316. doi: 10.1016/j.cct.2021.106316. Epub 2021 Feb 8.

Abstract

Assumptions made at design stage regarding the true treatment effect, background event rate and other factors may not always hold. Thus, long-term and large-scale studies may be designed with an interim analysis in order that the trials may be stopped early due to futility to save resource. There are many considerations of trial conducts for this type of trials. In this paper, we use a mock study to illustrate systematically the thinking and procedures for trial monitoring with a futility criterion for the interim results on a count data endpoint and a continuous endpoint. We focus on the discussions of blinded trial monitoring, the probability of meeting the futility criterion, conditional power/probability of success, Bayesian inference, potential delayed treatment effect and subgroup analysis. The experience should be applicable to future studies with similar features.

摘要

在设计阶段对真实治疗效果、背景事件发生率和其他因素的假设并非总是成立。因此,可能会设计长期和大规模的研究,并在中期分析时进行无效性检验,以便提前终止试验以节省资源。对于此类试验,有许多试验设计方面的考虑因素。本文使用模拟研究系统地说明在计数数据终点和连续终点的中期结果具有无效性标准的情况下,进行试验监测的思路和程序。我们重点讨论盲法试验监测、达到无效性标准的概率、条件功效/成功率、贝叶斯推断、潜在的延迟治疗效果和亚组分析。这一经验应该适用于具有类似特征的未来研究。

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