Suppr超能文献

用于优化序贯临床试验的贝叶斯自适应模型选择

Bayesian adaptive model selection for optimizing group sequential clinical trials.

作者信息

Wathen J Kyle, Thall Peter F

机构信息

Department of Biostatistics, University of Texas, M.D. Anderson Cancer Center, Box 447, 1515 Holcombe Boulevard, Houston, TX 77030, U.S.A.

出版信息

Stat Med. 2008 Nov 29;27(27):5586-604. doi: 10.1002/sim.3381.

Abstract

This article presents a new approach to the problem of deriving an optimal design for a randomized group sequential clinical trial based on right-censored event times. We are motivated by the fact that, if the proportional hazards assumption is not met, then a conventional design's actual power can differ substantially from its nominal value. We combine Bayesian decision theory, Bayesian model selection and forward simulation (FS) to obtain a group sequential procedure that maintains targeted false-positive rate and power, under a wide range of true event time distributions. At each interim analysis, the method adaptively chooses the most likely model and then applies the decision bounds that are optimal under the chosen model. A simulation study comparing this design with three conventional designs shows that, over a wide range of distributions, our proposed method performs at least as well as each conventional design, and in many cases it provides a much smaller trial.

摘要

本文提出了一种基于右删失事件时间推导随机分组序贯临床试验最优设计问题的新方法。我们的动机源于这样一个事实,即如果不满足比例风险假设,那么传统设计的实际功效可能与其名义值有很大差异。我们结合贝叶斯决策理论、贝叶斯模型选择和前向模拟(FS)来获得一种分组序贯程序,该程序在广泛的真实事件时间分布下保持目标假阳性率和功效。在每次期中分析时,该方法自适应地选择最可能的模型,然后应用在所选模型下最优的决策边界。一项将此设计与三种传统设计进行比较的模拟研究表明,在广泛的分布范围内,我们提出的方法至少与每种传统设计表现相当,并且在许多情况下它能提供规模小得多的试验。

相似文献

1
Bayesian adaptive model selection for optimizing group sequential clinical trials.
Stat Med. 2008 Nov 29;27(27):5586-604. doi: 10.1002/sim.3381.
2
A Bayesian Hybrid Adaptive Randomisation Design for Clinical Trials with Survival Outcomes.
Methods Inf Med. 2016;55(1):4-13. doi: 10.3414/ME14-01-0132. Epub 2015 Sep 25.
3
A Bayesian sequential design with adaptive randomization for 2-sided hypothesis test.
Pharm Stat. 2017 Nov;16(6):451-465. doi: 10.1002/pst.1830. Epub 2017 Oct 4.
6
A Bayesian group sequential design for randomized biosimilar clinical trials with adaptive information borrowing from historical data.
J Biopharm Stat. 2022 May 4;32(3):359-372. doi: 10.1080/10543406.2022.2080700. Epub 2022 Jun 9.
8
Bayesian designs and the control of frequentist characteristics: a practical solution.
Biometrics. 2015 Mar;71(1):218-226. doi: 10.1111/biom.12226. Epub 2014 Sep 5.
9
A Bayesian basket trial design using a calibrated Bayesian hierarchical model.
Clin Trials. 2018 Apr;15(2):149-158. doi: 10.1177/1740774518755122. Epub 2018 Mar 2.
10
Optimizing interim analysis timing for Bayesian adaptive commensurate designs.
Stat Med. 2020 Feb 20;39(4):424-437. doi: 10.1002/sim.8414. Epub 2019 Dec 4.

引用本文的文献

1
BAGS: A Bayesian Adaptive Group Sequential Trial Design With Subgroup-Specific Survival Comparisons.
J Am Stat Assoc. 2021;116(533):322-334. doi: 10.1080/01621459.2020.1837142. Epub 2020 Nov 30.
2
Comparing Bayesian early stopping boundaries for phase II clinical trials.
Pharm Stat. 2020 Nov;19(6):928-939. doi: 10.1002/pst.2046. Epub 2020 Jul 27.
3
Rapid, precise, and reliable measurement of delay discounting using a Bayesian learning algorithm.
Sci Rep. 2020 Jul 21;10(1):12091. doi: 10.1038/s41598-020-68587-x.
5
Bayesian Group Sequential Clinical Trial Design using Total Toxicity Burden and Progression-Free Survival.
J R Stat Soc Ser C Appl Stat. 2016 Feb;65(2):273-297. doi: 10.1111/rssc.12117. Epub 2015 Oct 26.
6
Controlled multi-arm platform design using predictive probability.
Stat Methods Med Res. 2018 Jan;27(1):65-78. doi: 10.1177/0962280215620696. Epub 2016 Jan 12.
7
Bayesian approach for assessing non-inferiority in a three-arm trial with pre-specified margin.
Stat Med. 2016 Feb 28;35(5):695-708. doi: 10.1002/sim.6746. Epub 2015 Oct 4.
8
Decision-theoretic designs for small trials and pilot studies: A review.
Stat Methods Med Res. 2016 Jun;25(3):1022-38. doi: 10.1177/0962280215588245. Epub 2015 Jun 5.
9
Optimizing Sedative Dose in Preterm Infants Undergoing Treatment for Respiratory Distress Syndrome.
J Am Stat Assoc. 2014 Sep 1;109(507):931-943. doi: 10.1080/01621459.2014.904789.
10
A Tutorial on Adaptive Design Optimization.
J Math Psychol. 2013 Jun;57(3-4):53-67. doi: 10.1016/j.jmp.2013.05.005.

本文引用的文献

4
Comparison of Bayesian with group sequential methods for monitoring clinical trials.
Control Clin Trials. 1989 Dec;10(4):357-67. doi: 10.1016/0197-2456(89)90001-9.
5
Practical problems in interim analyses, with particular regard to estimation.
Control Clin Trials. 1989 Dec;10(4 Suppl):209S-221S. doi: 10.1016/0197-2456(89)90059-7.
6
Group sequential designs using a family of type I error probability spending functions.
Stat Med. 1990 Dec;9(12):1439-45. doi: 10.1002/sim.4780091207.
7
A multiple testing procedure for clinical trials.
Biometrics. 1979 Sep;35(3):549-56.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验