Literature DB >> 23239078

A group sequential Holm procedure with multiple primary endpoints.

Yining Ye1, Ai Li, Lingyun Liu, Bin Yao.   

Abstract

We propose a group sequential Holm procedure when there are multiple primary endpoints. This method addresses multiplicities arising from multiple primary endpoints and from multiple analyses in a group sequential design. It has been shown to be a closed testing procedure and preserves the familywise error rate in the strong sense. When multiple endpoints are the only concern without an interim analysis, the method simplifies to the weighted Holm procedure. The proposed method is more powerful than the parallel group sequential method and avoids the need to anticipate the testing order as in the fixed sequence testing scheme.
Copyright © 2012 John Wiley & Sons, Ltd.

Mesh:

Year:  2012        PMID: 23239078     DOI: 10.1002/sim.5700

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


  8 in total

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Authors:  Ivair R Silva; Joshua J Gagne; Mehdi Najafzadeh; Martin Kulldorff
Journal:  Stat Med       Date:  2019-11-25       Impact factor: 2.373

Review 2.  Evidence-based statistical analysis and methods in biomedical research (SAMBR) checklists according to design features.

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Journal:  Cancer Rep (Hoboken)       Date:  2019-08-22

3.  A Rejection Principle for Sequential Tests of Multiple Hypotheses Controlling Familywise Error Rates.

Authors:  Jay Bartroff; Jinlin Song
Journal:  Scand Stat Theory Appl       Date:  2015-05-25       Impact factor: 1.396

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.  Sequential Tests of Multiple Hypotheses Controlling Type I and II Familywise Error Rates.

Authors:  Jay Bartroff; Jinlin Song
Journal:  J Stat Plan Inference       Date:  2014-10-01       Impact factor: 1.111

6.  On selecting the critical boundary functions in group-sequential trials with two time-to-event outcomes.

Authors:  Toshimitsu Hamasaki; H M James Hung; Chin-Fu Hsiao; Scott R Evans
Journal:  Contemp Clin Trials       Date:  2020-12-09       Impact factor: 2.226

7.  Multi-arm group sequential designs with a simultaneous stopping rule.

Authors:  S Urach; M Posch
Journal:  Stat Med       Date:  2016-08-23       Impact factor: 2.373

8.  Adaptive designs in clinical trials: why use them, and how to run and report them.

Authors:  Philip Pallmann; Alun W Bedding; Babak Choodari-Oskooei; Munyaradzi Dimairo; Laura Flight; Lisa V Hampson; Jane Holmes; Adrian P Mander; Lang'o Odondi; Matthew R Sydes; Sofía S Villar; James M S Wason; Christopher J Weir; Graham M Wheeler; Christina Yap; Thomas Jaki
Journal:  BMC Med       Date:  2018-02-28       Impact factor: 8.775

  8 in total

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