Literature DB >> 21432893

The inclusion of historical control data may reduce the power of a confirmatory study.

Robert L Cuffe1.   

Abstract

Large sample sizes in clinical trials increase the cost of clinical research and delay the availability of new treatments. Fewer patients could be recruited into clinical trials if historical data on the comparator could be used reliably in a trial's analysis. However, old trials may bias rather than augment data from a new trial if, for example, the standard of care has improved over time. A hierarchical model for the data from the current and historical trials decreases the weight given to the historical data in line with the discrepancy between the results from the different trials. This reduces the risk of substantial bias. This paper shows that this down-weighting is not sufficiently sensitive to differences in the response rates between trials. Motivated by recent trials in HIV, this paper proposes and examines a more conservative weighting of historical data. Simulation showed that both the standard hierarchical and the proposed weighting of historical data led to Type II error rates worse than those attained by ignoring the historical data completely. This underlines the risks of including historical data in the primary analysis of a trial for which strict control of error rates is paramount.
Copyright © 2011 John Wiley & Sons, Ltd.

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Year:  2011        PMID: 21432893     DOI: 10.1002/sim.4212

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


  8 in total

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Authors:  Philip S Boonstra; Jeremy Mg Taylor; Bhramar Mukherjee
Journal:  Stat Methods Med Res       Date:  2014-05-21       Impact factor: 3.021

2.  Does a digital regional nerve block improve the accuracy of noninvasive hemoglobin monitoring?

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Journal:  J Anesth       Date:  2012-08-01       Impact factor: 2.078

3.  Including historical data in the analysis of clinical trials: Is it worth the effort?

Authors:  Joost van Rosmalen; David Dejardin; Yvette van Norden; Bob Löwenberg; Emmanuel Lesaffre
Journal:  Stat Methods Med Res       Date:  2017-02-21       Impact factor: 3.021

4.  Incorporating individual historical controls and aggregate treatment effect estimates into a Bayesian survival trial: a simulation study.

Authors:  Caroline Brard; Lisa V Hampson; Nathalie Gaspar; Marie-Cécile Le Deley; Gwénaël Le Teuff
Journal:  BMC Med Res Methodol       Date:  2019-04-24       Impact factor: 4.615

5.  Power gains by using external information in clinical trials are typically not possible when requiring strict type I error control.

Authors:  Annette Kopp-Schneider; Silvia Calderazzo; Manuel Wiesenfarth
Journal:  Biom J       Date:  2019-07-02       Impact factor: 2.207

6.  Informed Bayesian survival analysis.

Authors:  František Bartoš; Frederik Aust; Julia M Haaf
Journal:  BMC Med Res Methodol       Date:  2022-09-10       Impact factor: 4.612

7.  "Threshold-crossing": A Useful Way to Establish the Counterfactual in Clinical Trials?

Authors:  H-G Eichler; B Bloechl-Daum; P Bauer; F Bretz; J Brown; L V Hampson; P Honig; M Krams; H Leufkens; R Lim; M M Lumpkin; M J Murphy; F Pignatti; M Posch; S Schneeweiss; M Trusheim; F Koenig
Journal:  Clin Pharmacol Ther       Date:  2016-10-19       Impact factor: 6.875

8.  Statistical consideration when adding new arms to ongoing clinical trials: the potentials and the caveats.

Authors:  Kim May Lee; Louise C Brown; Thomas Jaki; Nigel Stallard; James Wason
Journal:  Trials       Date:  2021-03-10       Impact factor: 2.279

  8 in total

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