Literature DB >> 19844944

Selection and bias--two hostile brothers.

Peter Bauer1, Franz Koenig, Werner Brannath, Martin Posch.   

Abstract

We consider the situation where in a first stage of a clinical trial several treatments are compared with a single control and the 'best' treatment(s) are selected in an interim analysis to be carried on to the second stage. We quantify the mean bias and mean square error of the conventional estimates after selection depending on the number of treatments and the selection time during the trial. The cases without or with reshuffling the planned sample size of the dropped treatments to the selected ones are investigated. The mean bias shows very different patterns depending on the selection rule and the unknown parameter values. We stress the fact that the quantification of the bias is possible only in designs with planned adaptivity where the design allows reacting to new evidence, but the decision rules are laid down in advance. Finally, we calculate the mean bias which arises in a simple but influential regulatory selection rule, to register a new medical therapy only when two pivotal trials have both proven an effect by a statistical test.

Mesh:

Substances:

Year:  2010        PMID: 19844944     DOI: 10.1002/sim.3716

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


  27 in total

1.  The Adaptive designs CONSORT Extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design.

Authors:  Munyaradzi Dimairo; Philip Pallmann; James Wason; Susan Todd; Thomas Jaki; Steven A Julious; Adrian P Mander; Christopher J Weir; Franz Koenig; Marc K Walton; Jon P Nicholl; Elizabeth Coates; Katie Biggs; Toshimitsu Hamasaki; Michael A Proschan; John A Scott; Yuki Ando; Daniel Hind; Douglas G Altman
Journal:  BMJ       Date:  2020-06-17

Review 2.  Comparison of the efficacy of lamivudine and telbivudine in the treatment of chronic hepatitis B: a systematic review.

Authors:  Shushan Zhao; Lanhua Tang; Xuegong Fan; Lizhang Chen; Rongrong Zhou; Xiahong Dai
Journal:  Virol J       Date:  2010-09-03       Impact factor: 4.099

3.  Phase II trial design with Bayesian adaptive randomization and predictive probability.

Authors:  Guosheng Yin; Nan Chen; J Jack Lee
Journal:  J R Stat Soc Ser C Appl Stat       Date:  2012-03-01       Impact factor: 1.864

4.  Response adaptive randomization procedures in seamless phase II/III clinical trials.

Authors:  Hongjian Zhu; Jin Piao; J Jack Lee; Feifang Hu; Lixin Zhang
Journal:  J Biopharm Stat       Date:  2019-08-27       Impact factor: 1.051

5.  Inference for multimarker adaptive enrichment trials.

Authors:  Richard Simon; Noah Simon
Journal:  Stat Med       Date:  2017-08-10       Impact factor: 2.373

6.  Twenty-five years of confirmatory adaptive designs: opportunities and pitfalls.

Authors:  Peter Bauer; Frank Bretz; Vladimir Dragalin; Franz König; Gernot Wassmer
Journal:  Stat Med       Date:  2015-03-16       Impact factor: 2.373

7.  Accounting for selection and correlation in the analysis of two-stage genome-wide association studies.

Authors:  David S Robertson; A Toby Prevost; Jack Bowden
Journal:  Biostatistics       Date:  2016-03-18       Impact factor: 5.899

8.  Conditionally unbiased estimation in phase II/III clinical trials with early stopping for futility.

Authors:  Peter K Kimani; Susan Todd; Nigel Stallard
Journal:  Stat Med       Date:  2013-02-15       Impact factor: 2.373

9.  The adaptive designs CONSORT extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design.

Authors:  Munyaradzi Dimairo; Philip Pallmann; James Wason; Susan Todd; Thomas Jaki; Steven A Julious; Adrian P Mander; Christopher J Weir; Franz Koenig; Marc K Walton; Jon P Nicholl; Elizabeth Coates; Katie Biggs; Toshimitsu Hamasaki; Michael A Proschan; John A Scott; Yuki Ando; Daniel Hind; Douglas G Altman
Journal:  Trials       Date:  2020-06-17       Impact factor: 2.279

10.  Impact of lack-of-benefit stopping rules on treatment effect estimates of two-arm multi-stage (TAMS) trials with time to event outcome.

Authors:  Babak Choodari-Oskooei; Mahesh K B Parmar; Patrick Royston; Jack Bowden
Journal:  Trials       Date:  2013-01-23       Impact factor: 2.279

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.