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Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials

In rare diseases, typically only a small number of patients are available for a randomized clinical trial. Nevertheless, it is not uncommon that more than one study is performed to evaluate a (new) treatment. Scarcity of available evidence makes it particularly valuable to pool the data in a meta‐an...

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Autores principales: Pateras, Konstantinos, Nikolakopoulos, Stavros, Roes, Kit C. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818503/
https://www.ncbi.nlm.nih.gov/pubmed/32767452
http://dx.doi.org/10.1002/pst.2053
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author Pateras, Konstantinos
Nikolakopoulos, Stavros
Roes, Kit C. B.
author_facet Pateras, Konstantinos
Nikolakopoulos, Stavros
Roes, Kit C. B.
author_sort Pateras, Konstantinos
collection PubMed
description In rare diseases, typically only a small number of patients are available for a randomized clinical trial. Nevertheless, it is not uncommon that more than one study is performed to evaluate a (new) treatment. Scarcity of available evidence makes it particularly valuable to pool the data in a meta‐analysis. When the primary outcome is binary, the small sample sizes increase the chance of observing zero events. The frequentist random‐effects model is known to induce bias and to result in improper interval estimation of the overall treatment effect in a meta‐analysis with zero events. Bayesian hierarchical modeling could be a promising alternative. Bayesian models are known for being sensitive to the choice of prior distributions for between‐study variance (heterogeneity) in sparse settings. In a rare disease setting, only limited data will be available to base the prior on, therefore, robustness of estimation is desirable. We performed an extensive and diverse simulation study, aiming to provide practitioners with advice on the choice of a sufficiently robust prior distribution shape for the heterogeneity parameter. Our results show that priors that place some concentrated mass on small τ values but do not restrict the density for example, the Uniform(−10, 10) heterogeneity prior on the log(τ (2)) scale, show robust 95% coverage combined with less overestimation of the overall treatment effect, across varying degrees of heterogeneity. We illustrate the results with meta‐analyzes of a few small trials.
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spelling pubmed-78185032021-01-26 Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials Pateras, Konstantinos Nikolakopoulos, Stavros Roes, Kit C. B. Pharm Stat Main Papers In rare diseases, typically only a small number of patients are available for a randomized clinical trial. Nevertheless, it is not uncommon that more than one study is performed to evaluate a (new) treatment. Scarcity of available evidence makes it particularly valuable to pool the data in a meta‐analysis. When the primary outcome is binary, the small sample sizes increase the chance of observing zero events. The frequentist random‐effects model is known to induce bias and to result in improper interval estimation of the overall treatment effect in a meta‐analysis with zero events. Bayesian hierarchical modeling could be a promising alternative. Bayesian models are known for being sensitive to the choice of prior distributions for between‐study variance (heterogeneity) in sparse settings. In a rare disease setting, only limited data will be available to base the prior on, therefore, robustness of estimation is desirable. We performed an extensive and diverse simulation study, aiming to provide practitioners with advice on the choice of a sufficiently robust prior distribution shape for the heterogeneity parameter. Our results show that priors that place some concentrated mass on small τ values but do not restrict the density for example, the Uniform(−10, 10) heterogeneity prior on the log(τ (2)) scale, show robust 95% coverage combined with less overestimation of the overall treatment effect, across varying degrees of heterogeneity. We illustrate the results with meta‐analyzes of a few small trials. John Wiley & Sons, Inc. 2020-08-06 2021 /pmc/articles/PMC7818503/ /pubmed/32767452 http://dx.doi.org/10.1002/pst.2053 Text en © 2020 The Authors. Pharmaceutical Statistics published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Main Papers
Pateras, Konstantinos
Nikolakopoulos, Stavros
Roes, Kit C. B.
Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
title Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
title_full Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
title_fullStr Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
title_full_unstemmed Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
title_short Prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
title_sort prior distributions for variance parameters in a sparse‐event meta‐analysis of a few small trials
topic Main Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818503/
https://www.ncbi.nlm.nih.gov/pubmed/32767452
http://dx.doi.org/10.1002/pst.2053
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