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Increasing the power of randomized trials comparing different treatment durations

When the optimal treatment duration is uncertain, a randomized trial may allocate patients to receive active treatment for different durations. We use an example where patients receive treatment for 0, 24, or 52 weeks. In this trial, patients in the 24-weeks and 52-weeks arms receive the same treatm...

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Autores principales: Ouyang, Yongdong, Qian, Hong, Yatham, Lakshmi N., Wong, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322686/
https://www.ncbi.nlm.nih.gov/pubmed/32617431
http://dx.doi.org/10.1016/j.conctc.2020.100588
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author Ouyang, Yongdong
Qian, Hong
Yatham, Lakshmi N.
Wong, Hubert
author_facet Ouyang, Yongdong
Qian, Hong
Yatham, Lakshmi N.
Wong, Hubert
author_sort Ouyang, Yongdong
collection PubMed
description When the optimal treatment duration is uncertain, a randomized trial may allocate patients to receive active treatment for different durations. We use an example where patients receive treatment for 0, 24, or 52 weeks. In this trial, patients in the 24-weeks and 52-weeks arms receive the same treatment during the first 24 weeks. This overlap allows for more powerful analyses than conventional pair-wise comparisons of arms. When the outcome is the time-to-event, the power for the 0-weeks versus 24-weeks comparison can be increased by including patients in the 52-weeks arm as patients in the 24-weeks arm for the first 24 weeks and censoring at 24 weeks. Furthermore, differences observed between the 24-weeks and 52-weeks arms during the first 24 weeks can only reflect noise. Hence, the comparison of these two arms should be restricted to only patients who remain on the study at 24 weeks and include only the events after 24 weeks. Through simulation, we show that modified analyses accounting for these considerations increase study power substantially. Moreover, if patients were allocated equally to the arms, then events or discontinuations during the first 24 weeks will reduce the number of patients available for the 24-weeks versus 52-weeks comparison, and hence the power of this analysis will be lower than that for the 0-weeks versus 24-weeks comparison. We present a sample size calculation procedure for equalizing the power of these two analyses. Typically, this allocation requires much larger sample sizes in the 24-weeks and 52-weeks arms than in the 0-week arm.
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spelling pubmed-73226862020-07-01 Increasing the power of randomized trials comparing different treatment durations Ouyang, Yongdong Qian, Hong Yatham, Lakshmi N. Wong, Hubert Contemp Clin Trials Commun Article When the optimal treatment duration is uncertain, a randomized trial may allocate patients to receive active treatment for different durations. We use an example where patients receive treatment for 0, 24, or 52 weeks. In this trial, patients in the 24-weeks and 52-weeks arms receive the same treatment during the first 24 weeks. This overlap allows for more powerful analyses than conventional pair-wise comparisons of arms. When the outcome is the time-to-event, the power for the 0-weeks versus 24-weeks comparison can be increased by including patients in the 52-weeks arm as patients in the 24-weeks arm for the first 24 weeks and censoring at 24 weeks. Furthermore, differences observed between the 24-weeks and 52-weeks arms during the first 24 weeks can only reflect noise. Hence, the comparison of these two arms should be restricted to only patients who remain on the study at 24 weeks and include only the events after 24 weeks. Through simulation, we show that modified analyses accounting for these considerations increase study power substantially. Moreover, if patients were allocated equally to the arms, then events or discontinuations during the first 24 weeks will reduce the number of patients available for the 24-weeks versus 52-weeks comparison, and hence the power of this analysis will be lower than that for the 0-weeks versus 24-weeks comparison. We present a sample size calculation procedure for equalizing the power of these two analyses. Typically, this allocation requires much larger sample sizes in the 24-weeks and 52-weeks arms than in the 0-week arm. Elsevier 2020-06-10 /pmc/articles/PMC7322686/ /pubmed/32617431 http://dx.doi.org/10.1016/j.conctc.2020.100588 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ouyang, Yongdong
Qian, Hong
Yatham, Lakshmi N.
Wong, Hubert
Increasing the power of randomized trials comparing different treatment durations
title Increasing the power of randomized trials comparing different treatment durations
title_full Increasing the power of randomized trials comparing different treatment durations
title_fullStr Increasing the power of randomized trials comparing different treatment durations
title_full_unstemmed Increasing the power of randomized trials comparing different treatment durations
title_short Increasing the power of randomized trials comparing different treatment durations
title_sort increasing the power of randomized trials comparing different treatment durations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322686/
https://www.ncbi.nlm.nih.gov/pubmed/32617431
http://dx.doi.org/10.1016/j.conctc.2020.100588
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