Literature DB >> 33105524

A framework for considering the risk-benefit trade-off in designing noninferiority trials using composite outcome approaches.

Grace Montepiedra1, Ritesh Ramchandani1, Sachiko Miyahara1, Soyeon Kim2.   

Abstract

When a new treatment regimen is expected to have comparable or slightly worse efficacy to that of the control regimen but has benefits in other domains such as safety and tolerability, a noninferiority (NI) trial may be appropriate but is fraught with difficulty in justifying an acceptable NI margin that is based on both clinical and statistical input. To overcome this, we propose to utilize composite risk-benefit outcomes that combine elements from domains of importance (eg, efficacy, safety, and tolerability). The composite outcome itself may be analyzed using a superiority framework, or it can be used as a tool at the design stage of a NI trial for selecting an NI margin for efficacy that balances changes in risks and benefits. In the latter case, the choice of NI margin may be based on a novel quantity called the maximum allowable decrease in efficacy (MADE), defined as the marginal difference in efficacy between arms that would yield a null treatment effect for the composite outcome given an assumed distribution for the composite outcome. We observe that MADE: (1) is larger when the safety improvement for the experimental arm is larger, (2) depends on the association between the efficacy and safety outcomes, and (3) depends on the control arm efficacy rate. We use a numerical example for power comparisons between a superiority test for the composite outcome vs a noninferiority test for efficacy using the MADE as the NI margin, and apply the methods to a TB treatment trial.
© 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  clinical trial; composite outcome; noninferiority margin; risk-benefit; trial design; tuberculosis

Year:  2020        PMID: 33105524      PMCID: PMC7770022          DOI: 10.1002/sim.8777

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


  36 in total

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5.  One Month of Rifapentine plus Isoniazid to Prevent HIV-Related Tuberculosis.

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Journal:  N Engl J Med       Date:  2019-03-14       Impact factor: 91.245

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Journal:  N Engl J Med       Date:  2014-01-23       Impact factor: 91.245

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Authors:  Corinne S Merle; Katherine Fielding; Omou Bah Sow; Martin Gninafon; Mame B Lo; Thuli Mthiyane; Joseph Odhiambo; Evans Amukoye; Boubacar Bah; Ferdinand Kassa; Alimatou N'Diaye; Roxana Rustomjee; Bouke C de Jong; John Horton; Christian Perronne; Charalambos Sismanidis; Olivier Lapujade; Piero L Olliaro; Christian Lienhardt
Journal:  N Engl J Med       Date:  2014-10-23       Impact factor: 91.245

10.  Totality of outcomes: A different paradigm in assessing interventions for treatment of tuberculosis.

Authors:  Grace Montepiedra; Courtney M Yuen; Michael L Rich; Scott R Evans
Journal:  J Clin Tuberc Other Mycobact Dis       Date:  2016-08
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