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Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints
We investigate the effect of the choice of parameterisation of meta-analytic models and related uncertainty on the validation of surrogate endpoints. Different meta-analytical approaches take into account different levels of uncertainty which may impact on the accuracy of the predictions of treatmen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642004/ https://www.ncbi.nlm.nih.gov/pubmed/26271918 http://dx.doi.org/10.1177/0962280215597260 |
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author | Bujkiewicz, Sylwia Thompson, John R Spata, Enti Abrams, Keith R |
author_facet | Bujkiewicz, Sylwia Thompson, John R Spata, Enti Abrams, Keith R |
author_sort | Bujkiewicz, Sylwia |
collection | PubMed |
description | We investigate the effect of the choice of parameterisation of meta-analytic models and related uncertainty on the validation of surrogate endpoints. Different meta-analytical approaches take into account different levels of uncertainty which may impact on the accuracy of the predictions of treatment effect on the target outcome from the treatment effect on a surrogate endpoint obtained from these models. A range of Bayesian as well as frequentist meta-analytical methods are implemented using illustrative examples in relapsing–remitting multiple sclerosis, where the treatment effect on disability worsening is the primary outcome of interest in healthcare evaluation, while the effect on relapse rate is considered as a potential surrogate to the effect on disability progression, and in gastric cancer, where the disease-free survival has been shown to be a good surrogate endpoint to the overall survival. Sensitivity analysis was carried out to assess the impact of distributional assumptions on the predictions. Also, sensitivity to modelling assumptions and performance of the models were investigated by simulation. Although different methods can predict mean true outcome almost equally well, inclusion of uncertainty around all relevant parameters of the model may lead to less certain and hence more conservative predictions. When investigating endpoints as candidate surrogate outcomes, a careful choice of the meta-analytical approach has to be made. Models underestimating the uncertainty of available evidence may lead to overoptimistic predictions which can then have an effect on decisions made based on such predictions. |
format | Online Article Text |
id | pubmed-5642004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-56420042017-10-26 Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints Bujkiewicz, Sylwia Thompson, John R Spata, Enti Abrams, Keith R Stat Methods Med Res Regular Articles We investigate the effect of the choice of parameterisation of meta-analytic models and related uncertainty on the validation of surrogate endpoints. Different meta-analytical approaches take into account different levels of uncertainty which may impact on the accuracy of the predictions of treatment effect on the target outcome from the treatment effect on a surrogate endpoint obtained from these models. A range of Bayesian as well as frequentist meta-analytical methods are implemented using illustrative examples in relapsing–remitting multiple sclerosis, where the treatment effect on disability worsening is the primary outcome of interest in healthcare evaluation, while the effect on relapse rate is considered as a potential surrogate to the effect on disability progression, and in gastric cancer, where the disease-free survival has been shown to be a good surrogate endpoint to the overall survival. Sensitivity analysis was carried out to assess the impact of distributional assumptions on the predictions. Also, sensitivity to modelling assumptions and performance of the models were investigated by simulation. Although different methods can predict mean true outcome almost equally well, inclusion of uncertainty around all relevant parameters of the model may lead to less certain and hence more conservative predictions. When investigating endpoints as candidate surrogate outcomes, a careful choice of the meta-analytical approach has to be made. Models underestimating the uncertainty of available evidence may lead to overoptimistic predictions which can then have an effect on decisions made based on such predictions. SAGE Publications 2015-08-13 2017-10 /pmc/articles/PMC5642004/ /pubmed/26271918 http://dx.doi.org/10.1177/0962280215597260 Text en © The Author(s) 2015 http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution 3.0 License (http://www.creativecommons.org/licenses/by/3.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Regular Articles Bujkiewicz, Sylwia Thompson, John R Spata, Enti Abrams, Keith R Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints |
title | Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints |
title_full | Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints |
title_fullStr | Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints |
title_full_unstemmed | Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints |
title_short | Uncertainty in the Bayesian meta-analysis of normally distributed surrogate endpoints |
title_sort | uncertainty in the bayesian meta-analysis of normally distributed surrogate endpoints |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642004/ https://www.ncbi.nlm.nih.gov/pubmed/26271918 http://dx.doi.org/10.1177/0962280215597260 |
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