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Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials
Model-based meta-analysis (MBMA) is an approach that integrates relevant summary level data from heterogeneously designed randomized controlled trials (RCTs). This study not only evaluated the predictability of a published MBMA for forced expiratory volume in one second (FEV(1)) and its link to annu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374752/ https://www.ncbi.nlm.nih.gov/pubmed/36947282 http://dx.doi.org/10.1007/s10928-023-09853-z |
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author | Llanos-Paez, Carolina Ambery, Claire Yang, Shuying Beerahee, Misba Plan, Elodie L. Karlsson, Mats O. |
author_facet | Llanos-Paez, Carolina Ambery, Claire Yang, Shuying Beerahee, Misba Plan, Elodie L. Karlsson, Mats O. |
author_sort | Llanos-Paez, Carolina |
collection | PubMed |
description | Model-based meta-analysis (MBMA) is an approach that integrates relevant summary level data from heterogeneously designed randomized controlled trials (RCTs). This study not only evaluated the predictability of a published MBMA for forced expiratory volume in one second (FEV(1)) and its link to annual exacerbation rate in patients with chronic obstructive pulmonary disease (COPD) but also included data from new RCTs. A comparative effectiveness analysis across all drugs was also performed. Aggregated level data were collected from RCTs published between July 2013 and November 2020 (n = 132 references comprising 156 studies) and combined with data used in the legacy MBMA (published RCTs up to July 2013 - n = 142). The augmented data (n = 298) were used to evaluate the predictive performance of the published MBMA using goodness-of-fit plots for assessment. Furthermore, the model was extended including drugs that were not available before July 2013, estimating a new set of parameters. The legacy MBMA model predicted the post-2013 FEV(1) data well, and new estimated parameters were similar to those of drugs in the same class. However, the exacerbation model overpredicted the post-2013 mean annual exacerbation rate data. Inclusion of year when the study started on the pre-treatment placebo rate improved the model predictive performance perhaps explaining potential improvements in the disease management over time. The addition of new data to the legacy COPD MBMA enabled a more robust model with increased predictability performance for both endpoints FEV(1) and mean annual exacerbation rate. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10928-023-09853-z. |
format | Online Article Text |
id | pubmed-10374752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-103747522023-07-29 Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials Llanos-Paez, Carolina Ambery, Claire Yang, Shuying Beerahee, Misba Plan, Elodie L. Karlsson, Mats O. J Pharmacokinet Pharmacodyn Original Paper Model-based meta-analysis (MBMA) is an approach that integrates relevant summary level data from heterogeneously designed randomized controlled trials (RCTs). This study not only evaluated the predictability of a published MBMA for forced expiratory volume in one second (FEV(1)) and its link to annual exacerbation rate in patients with chronic obstructive pulmonary disease (COPD) but also included data from new RCTs. A comparative effectiveness analysis across all drugs was also performed. Aggregated level data were collected from RCTs published between July 2013 and November 2020 (n = 132 references comprising 156 studies) and combined with data used in the legacy MBMA (published RCTs up to July 2013 - n = 142). The augmented data (n = 298) were used to evaluate the predictive performance of the published MBMA using goodness-of-fit plots for assessment. Furthermore, the model was extended including drugs that were not available before July 2013, estimating a new set of parameters. The legacy MBMA model predicted the post-2013 FEV(1) data well, and new estimated parameters were similar to those of drugs in the same class. However, the exacerbation model overpredicted the post-2013 mean annual exacerbation rate data. Inclusion of year when the study started on the pre-treatment placebo rate improved the model predictive performance perhaps explaining potential improvements in the disease management over time. The addition of new data to the legacy COPD MBMA enabled a more robust model with increased predictability performance for both endpoints FEV(1) and mean annual exacerbation rate. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10928-023-09853-z. Springer US 2023-03-22 2023 /pmc/articles/PMC10374752/ /pubmed/36947282 http://dx.doi.org/10.1007/s10928-023-09853-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Llanos-Paez, Carolina Ambery, Claire Yang, Shuying Beerahee, Misba Plan, Elodie L. Karlsson, Mats O. Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials |
title | Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials |
title_full | Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials |
title_fullStr | Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials |
title_full_unstemmed | Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials |
title_short | Joint longitudinal model-based meta-analysis of FEV(1) and exacerbation rate in randomized COPD trials |
title_sort | joint longitudinal model-based meta-analysis of fev(1) and exacerbation rate in randomized copd trials |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374752/ https://www.ncbi.nlm.nih.gov/pubmed/36947282 http://dx.doi.org/10.1007/s10928-023-09853-z |
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