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A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis

BACKGROUND: Motivated by the setting of clinical trials in low back pain, this work investigated statistical methods to identify patient subgroups for which there is a large treatment effect (treatment by subgroup interaction). Statistical tests for interaction are often underpowered. Individual pat...

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Detalles Bibliográficos
Autores principales: Mistry, Dipesh, Stallard, Nigel, Underwood, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900744/
https://www.ncbi.nlm.nih.gov/pubmed/29383818
http://dx.doi.org/10.1002/sim.7609
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author Mistry, Dipesh
Stallard, Nigel
Underwood, Martin
author_facet Mistry, Dipesh
Stallard, Nigel
Underwood, Martin
author_sort Mistry, Dipesh
collection PubMed
description BACKGROUND: Motivated by the setting of clinical trials in low back pain, this work investigated statistical methods to identify patient subgroups for which there is a large treatment effect (treatment by subgroup interaction). Statistical tests for interaction are often underpowered. Individual patient data (IPD) meta‐analyses provide a framework with improved statistical power to investigate subgroups. However, conventional approaches to subgroup analyses applied in both a single trial setting and an IPD setting have a number of issues, one of them being that factors used to define subgroups are investigated one at a time. As individuals have multiple characteristics that may be related to response to treatment, alternative exploratory statistical methods are required. METHODS: Tree‐based methods are a promising alternative that systematically searches the covariate space to identify subgroups defined by multiple characteristics. A tree method in particular, SIDES, is described and extended for application in an IPD meta‐analyses setting by incorporating fixed‐effects and random‐effects models to account for between‐trial variation. The performance of the proposed extension was assessed using simulation studies. The proposed method was then applied to an IPD low back pain dataset. RESULTS: The simulation studies found that the extended IPD‐SIDES method performed well in detecting subgroups especially in the presence of large between‐trial variation. The IPD‐SIDES method identified subgroups with enhanced treatment effect when applied to the low back pain data. CONCLUSIONS: This work proposes an exploratory statistical approach for subgroup analyses applicable in any research discipline where subgroup analyses in an IPD meta‐analysis setting are of interest.
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spelling pubmed-59007442018-04-23 A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis Mistry, Dipesh Stallard, Nigel Underwood, Martin Stat Med Research Articles BACKGROUND: Motivated by the setting of clinical trials in low back pain, this work investigated statistical methods to identify patient subgroups for which there is a large treatment effect (treatment by subgroup interaction). Statistical tests for interaction are often underpowered. Individual patient data (IPD) meta‐analyses provide a framework with improved statistical power to investigate subgroups. However, conventional approaches to subgroup analyses applied in both a single trial setting and an IPD setting have a number of issues, one of them being that factors used to define subgroups are investigated one at a time. As individuals have multiple characteristics that may be related to response to treatment, alternative exploratory statistical methods are required. METHODS: Tree‐based methods are a promising alternative that systematically searches the covariate space to identify subgroups defined by multiple characteristics. A tree method in particular, SIDES, is described and extended for application in an IPD meta‐analyses setting by incorporating fixed‐effects and random‐effects models to account for between‐trial variation. The performance of the proposed extension was assessed using simulation studies. The proposed method was then applied to an IPD low back pain dataset. RESULTS: The simulation studies found that the extended IPD‐SIDES method performed well in detecting subgroups especially in the presence of large between‐trial variation. The IPD‐SIDES method identified subgroups with enhanced treatment effect when applied to the low back pain data. CONCLUSIONS: This work proposes an exploratory statistical approach for subgroup analyses applicable in any research discipline where subgroup analyses in an IPD meta‐analysis setting are of interest. John Wiley and Sons Inc. 2018-01-31 2018-04-30 /pmc/articles/PMC5900744/ /pubmed/29383818 http://dx.doi.org/10.1002/sim.7609 Text en © 2018 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Mistry, Dipesh
Stallard, Nigel
Underwood, Martin
A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
title A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
title_full A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
title_fullStr A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
title_full_unstemmed A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
title_short A recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
title_sort recursive partitioning approach for subgroup identification in individual patient data meta‐analysis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900744/
https://www.ncbi.nlm.nih.gov/pubmed/29383818
http://dx.doi.org/10.1002/sim.7609
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