Literature DB >> 24933121

Alternative views on setting clinical trial futility criteria.

Paul Gallo1, Lu Mao, Vivian H Shih.   

Abstract

A feature increasingly utilized in clinical trial practice is to allow a study to stop early when it seems unlikely to achieve its primary efficacy objectives. This is commonly referred to as stopping for futility, and can be motivated by ethical and financial considerations. A number of methods for addressing futility have been described in the literature, including rules based upon conditional power, predictive probability, beta spending functions, and others. We consider futility stopping from the point of view of quantifying and providing an objective sensible balance between risks of incorrect decisions (e.g., stopping trials which should continue, and continuing trials which should stop), and discuss how specific considerations within a trial can lead to choice of a sensible scheme. This approach is not specific to any particular scales in the literature such as those just mentioned, and we describe interrelationships among criteria expressed on different scales. As futility may be evaluated multiple times in a long-term trial and the amount of information available at scheduled interim analyses may be difficult to predict in advance, we present a specific optimality criterion and discuss which of the familiar scales tend to produce schemes simple to describe and implement, and with better behavior across different timepoints at which futility might be evaluated.

Keywords:  Conditional power; Futility; Interim analysis; Predictive probability

Mesh:

Year:  2014        PMID: 24933121     DOI: 10.1080/10543406.2014.932285

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  7 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

2.  Superiority of combining two independent trials in interim futility analysis.

Authors:  Qiqi Deng; Ying-Ying Zhang; Dooti Roy; Ming-Hui Chen
Journal:  Stat Methods Med Res       Date:  2019-04-08       Impact factor: 3.021

3.  Interim Monitoring for Futility in Clinical Trials with Two Co-primary Endpoints Using Prediction.

Authors:  Koko Asakura; Scott R Evans; Toshimitsu Hamasaki
Journal:  Stat Biopharm Res       Date:  2019-11-04       Impact factor: 1.452

4.  Patient recruitment strategies for adaptive enrichment designs with time-to-event endpoints.

Authors:  Ryuji Uozumi; Shinjo Yada; Atsushi Kawaguchi
Journal:  BMC Med Res Methodol       Date:  2019-07-22       Impact factor: 4.615

5.  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

6.  Optimality criteria for futility stopping boundaries for group sequential designs with a continuous endpoint.

Authors:  Xieran Li; Carolin Herrmann; Geraldine Rauch
Journal:  BMC Med Res Methodol       Date:  2020-11-05       Impact factor: 4.615

7.  Decision rules for identifying combination therapies in open-entry, randomized controlled platform trials.

Authors:  Elias Laurin Meyer; Peter Mesenbrink; Cornelia Dunger-Baldauf; Ekkehard Glimm; Yuhan Li; Franz König
Journal:  Pharm Stat       Date:  2022-01-31       Impact factor: 1.234

  7 in total

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