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Individual patient data meta-analysis of survival data using Poisson regression models
BACKGROUND: An Individual Patient Data (IPD) meta-analysis is often considered the gold-standard for synthesising survival data from clinical trials. An IPD meta-analysis can be achieved by either a two-stage or a one-stage approach, depending on whether the trials are analysed separately or simulta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398853/ https://www.ncbi.nlm.nih.gov/pubmed/22443286 http://dx.doi.org/10.1186/1471-2288-12-34 |
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author | Crowther, Michael J Riley, Richard D Staessen, Jan A Wang, Jiguang Gueyffier, Francois Lambert, Paul C |
author_facet | Crowther, Michael J Riley, Richard D Staessen, Jan A Wang, Jiguang Gueyffier, Francois Lambert, Paul C |
author_sort | Crowther, Michael J |
collection | PubMed |
description | BACKGROUND: An Individual Patient Data (IPD) meta-analysis is often considered the gold-standard for synthesising survival data from clinical trials. An IPD meta-analysis can be achieved by either a two-stage or a one-stage approach, depending on whether the trials are analysed separately or simultaneously. A range of one-stage hierarchical Cox models have been previously proposed, but these are known to be computationally intensive and are not currently available in all standard statistical software. We describe an alternative approach using Poisson based Generalised Linear Models (GLMs). METHODS: We illustrate, through application and simulation, the Poisson approach both classically and in a Bayesian framework, in two-stage and one-stage approaches. We outline the benefits of our one-stage approach through extension to modelling treatment-covariate interactions and non-proportional hazards. Ten trials of hypertension treatment, with all-cause death the outcome of interest, are used to apply and assess the approach. RESULTS: We show that the Poisson approach obtains almost identical estimates to the Cox model, is additionally computationally efficient and directly estimates the baseline hazard. Some downward bias is observed in classical estimates of the heterogeneity in the treatment effect, with improved performance from the Bayesian approach. CONCLUSION: Our approach provides a highly flexible and computationally efficient framework, available in all standard statistical software, to the investigation of not only heterogeneity, but the presence of non-proportional hazards and treatment effect modifiers. |
format | Online Article Text |
id | pubmed-3398853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33988532012-07-18 Individual patient data meta-analysis of survival data using Poisson regression models Crowther, Michael J Riley, Richard D Staessen, Jan A Wang, Jiguang Gueyffier, Francois Lambert, Paul C BMC Med Res Methodol Research Article BACKGROUND: An Individual Patient Data (IPD) meta-analysis is often considered the gold-standard for synthesising survival data from clinical trials. An IPD meta-analysis can be achieved by either a two-stage or a one-stage approach, depending on whether the trials are analysed separately or simultaneously. A range of one-stage hierarchical Cox models have been previously proposed, but these are known to be computationally intensive and are not currently available in all standard statistical software. We describe an alternative approach using Poisson based Generalised Linear Models (GLMs). METHODS: We illustrate, through application and simulation, the Poisson approach both classically and in a Bayesian framework, in two-stage and one-stage approaches. We outline the benefits of our one-stage approach through extension to modelling treatment-covariate interactions and non-proportional hazards. Ten trials of hypertension treatment, with all-cause death the outcome of interest, are used to apply and assess the approach. RESULTS: We show that the Poisson approach obtains almost identical estimates to the Cox model, is additionally computationally efficient and directly estimates the baseline hazard. Some downward bias is observed in classical estimates of the heterogeneity in the treatment effect, with improved performance from the Bayesian approach. CONCLUSION: Our approach provides a highly flexible and computationally efficient framework, available in all standard statistical software, to the investigation of not only heterogeneity, but the presence of non-proportional hazards and treatment effect modifiers. BioMed Central 2012-03-23 /pmc/articles/PMC3398853/ /pubmed/22443286 http://dx.doi.org/10.1186/1471-2288-12-34 Text en Copyright ©2012 Crowther et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Crowther, Michael J Riley, Richard D Staessen, Jan A Wang, Jiguang Gueyffier, Francois Lambert, Paul C Individual patient data meta-analysis of survival data using Poisson regression models |
title | Individual patient data meta-analysis of survival data using Poisson regression models |
title_full | Individual patient data meta-analysis of survival data using Poisson regression models |
title_fullStr | Individual patient data meta-analysis of survival data using Poisson regression models |
title_full_unstemmed | Individual patient data meta-analysis of survival data using Poisson regression models |
title_short | Individual patient data meta-analysis of survival data using Poisson regression models |
title_sort | individual patient data meta-analysis of survival data using poisson regression models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398853/ https://www.ncbi.nlm.nih.gov/pubmed/22443286 http://dx.doi.org/10.1186/1471-2288-12-34 |
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