三阶段临床试验中样本量的重新计算及其评估。

IF 3.9 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Björn Bokelmann, Geraldine Rauch, Jan Meis, Meinhard Kieser, Carolin Herrmann
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引用次数: 0

摘要

背景:在临床试验中,确定足够的样本量是一项具有挑战性的任务,这主要是由于效应大小值和干扰参数的不确定性。处理这种不确定性的一种方法是重新计算样本量。在此基础上进行中期分析,调整剩余试验的样本量。除少数例外,以往的文献只研究了两阶段试验中重新计算的可能性:在我们的研究中,我们探讨了三阶段试验中样本量的重新计算,即预先计划了两次中期分析的试验。我们展示了如何修改两阶段试验的重新计算规则,使其适用于三阶段试验。我们还说明了如何将最近针对两阶段试验重新计算提出的绩效衡量标准(条件绩效评分)应用于评估三阶段试验的重新计算规则,并从全局角度描述了这些试验的绩效评估。为了评估重新计算在三阶段试验中的潜力,我们在模拟研究中比较了两阶段分组顺序设计和三阶段分组顺序设计,以及带有重新计算的多个三阶段设计:结果:与两阶段设计相比,我们观察到三阶段设计在功率和预期样本量方面具有明显的优势,但重新计算规则的优势似乎不太明显,而且取决于所应用的绩效衡量标准:结论:样本量重新计算也适用于三阶段设计。结论:样本量重新计算也适用于三阶段设计。然而,重新计算带来的益处取决于哪些试验特征对申请人最为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sample size recalculation in three-stage clinical trials and its evaluation.

Background: In clinical trials, the determination of an adequate sample size is a challenging task, mainly due to the uncertainty about the value of the effect size and nuisance parameters. One method to deal with this uncertainty is a sample size recalculation. Thereby, an interim analysis is performed based on which the sample size for the remaining trial is adapted. With few exceptions, previous literature has only examined the potential of recalculation in two-stage trials.

Methods: In our research, we address sample size recalculation in three-stage trials, i.e. trials with two pre-planned interim analyses. We show how recalculation rules from two-stage trials can be modified to be applicable to three-stage trials. We also illustrate how a performance measure, recently suggested for two-stage trial recalculation (the conditional performance score) can be applied to evaluate recalculation rules in three-stage trials, and we describe performance evaluation in those trials from the global point of view. To assess the potential of recalculation in three-stage trials, we compare, in a simulation study, two-stage group sequential designs with three-stage group sequential designs as well as multiple three-stage designs with recalculation.

Results: While we observe a notable favorable effect in terms of power and expected sample size by using three-stage designs compared to two-stage designs, the benefits of recalculation rules appear less clear and are dependent on the performance measures applied.

Conclusions: Sample size recalculation is also applicable in three-stage designs. However, the extent to which recalculation brings benefits depends on which trial characteristics are most important to the applicants.

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来源期刊
BMC Medical Research Methodology
BMC Medical Research Methodology 医学-卫生保健
CiteScore
6.50
自引率
2.50%
发文量
298
审稿时长
3-8 weeks
期刊介绍: BMC Medical Research Methodology is an open access journal publishing original peer-reviewed research articles in methodological approaches to healthcare research. Articles on the methodology of epidemiological research, clinical trials and meta-analysis/systematic review are particularly encouraged, as are empirical studies of the associations between choice of methodology and study outcomes. BMC Medical Research Methodology does not aim to publish articles describing scientific methods or techniques: these should be directed to the BMC journal covering the relevant biomedical subject area.
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