Literature DB >> 18752257

Bayesian adaptive model selection for optimizing group sequential clinical trials.

J Kyle Wathen1, Peter F Thall.   

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. Copyright (c) 2008 John Wiley & Sons, Ltd.

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Year:  2008        PMID: 18752257      PMCID: PMC5587123          DOI: 10.1002/sim.3381

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  7 in total

1.  Group sequential designs using a family of type I error probability spending functions.

Authors:  I K Hwang; W J Shih; J S De Cani
Journal:  Stat Med       Date:  1990-12       Impact factor: 2.373

2.  Approaches for optimal sequential decision analysis in clinical trials.

Authors:  B P Carlin; J B Kadane; A E Gelfand
Journal:  Biometrics       Date:  1998-09       Impact factor: 2.571

3.  Practical problems in interim analyses, with particular regard to estimation.

Authors:  S J Pocock; M D Hughes
Journal:  Control Clin Trials       Date:  1989-12

4.  One-sided sequential stopping boundaries for clinical trials: a decision-theoretic approach.

Authors:  D A Berry; C H Ho
Journal:  Biometrics       Date:  1988-03       Impact factor: 2.571

5.  Comparison of Bayesian with group sequential methods for monitoring clinical trials.

Authors:  L S Freedman; D J Spiegelhalter
Journal:  Control Clin Trials       Date:  1989-12

6.  Approximately optimal one-parameter boundaries for group sequential trials.

Authors:  S K Wang; A A Tsiatis
Journal:  Biometrics       Date:  1987-03       Impact factor: 2.571

7.  A multiple testing procedure for clinical trials.

Authors:  P C O'Brien; T R Fleming
Journal:  Biometrics       Date:  1979-09       Impact factor: 2.571

  7 in total
  10 in total

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Authors:  Peter F Thall; Hoang Q Nguyen; Sarah Zohar; Pierre Maton
Journal:  J Am Stat Assoc       Date:  2014-09-01       Impact factor: 5.033

2.  Optimal dynamic regimes: presenting a case for predictive inference.

Authors:  Elja Arjas; Olli Saarela
Journal:  Int J Biostat       Date:  2010-03-03       Impact factor: 0.968

3.  A Tutorial on Adaptive Design Optimization.

Authors:  Jay I Myung; Daniel R Cavagnaro; Mark A Pitt
Journal:  J Math Psychol       Date:  2013-06       Impact factor: 2.223

4.  BAGS: A Bayesian Adaptive Group Sequential Trial Design With Subgroup-Specific Survival Comparisons.

Authors:  Ruitao Lin; Peter F Thall; Ying Yuan
Journal:  J Am Stat Assoc       Date:  2020-11-30       Impact factor: 4.369

5.  Bayesian Group Sequential Clinical Trial Design using Total Toxicity Burden and Progression-Free Survival.

Authors:  Brian P Hobbs; Peter F Thall; Steven H Lin
Journal:  J R Stat Soc Ser C Appl Stat       Date:  2015-10-26       Impact factor: 1.864

6.  Challenges in the evaluation, consent, ethics and history of early clinical trials - Implications of the Tuskegee 'trial' for safer and more ethical clinical trials.

Authors:  Pedro R Lowenstein; Elijah D Lowenstein; Maria G Castro
Journal:  Curr Opin Mol Ther       Date:  2009-10

7.  Controlled multi-arm platform design using predictive probability.

Authors:  Brian P Hobbs; Nan Chen; J Jack Lee
Journal:  Stat Methods Med Res       Date:  2016-01-12       Impact factor: 3.021

8.  Comparing Bayesian early stopping boundaries for phase II clinical trials.

Authors:  Liyun Jiang; Fangrong Yan; Peter F Thall; Xuelin Huang
Journal:  Pharm Stat       Date:  2020-07-27       Impact factor: 1.234

Review 9.  Decision-theoretic designs for small trials and pilot studies: A review.

Authors:  Siew Wan Hee; Thomas Hamborg; Simon Day; Jason Madan; Frank Miller; Martin Posch; Sarah Zohar; Nigel Stallard
Journal:  Stat Methods Med Res       Date:  2015-06-05       Impact factor: 3.021

10.  Active SAmpling Protocol (ASAP) to Optimize Individual Neurocognitive Hypothesis Testing: A BCI-Inspired Dynamic Experimental Design.

Authors:  Gaëtan Sanchez; Françoise Lecaignard; Anatole Otman; Emmanuel Maby; Jérémie Mattout
Journal:  Front Hum Neurosci       Date:  2016-07-07       Impact factor: 3.169

  10 in total

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