Cargando…

Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients

BACKGROUND: Platform trials are well-known for their ability to investigate multiple arms on heterogeneous patient populations and their flexibility to add/drop treatment arms due to efficacy/lack of efficacy. Because of their complexity, it is important to develop highly optimized, transparent, and...

Descripción completa

Detalles Bibliográficos
Autores principales: Gao, Guangyi, Gajewski, Byron J., Wick, Jo, Beall, Jonathan, Saver, Jeffrey L., Meinzer, Caitlyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446515/
https://www.ncbi.nlm.nih.gov/pubmed/36068547
http://dx.doi.org/10.1186/s13063-022-06664-4
_version_ 1784783658375184384
author Gao, Guangyi
Gajewski, Byron J.
Wick, Jo
Beall, Jonathan
Saver, Jeffrey L.
Meinzer, Caitlyn
author_facet Gao, Guangyi
Gajewski, Byron J.
Wick, Jo
Beall, Jonathan
Saver, Jeffrey L.
Meinzer, Caitlyn
author_sort Gao, Guangyi
collection PubMed
description BACKGROUND: Platform trials are well-known for their ability to investigate multiple arms on heterogeneous patient populations and their flexibility to add/drop treatment arms due to efficacy/lack of efficacy. Because of their complexity, it is important to develop highly optimized, transparent, and rigorous designs that are cost-efficient, offer high statistical power, maximize patient benefit, and are robust to changes over time. METHODS: To address these needs, we present a Bayesian platform trial design based on a beta-binomial model for binary outcomes that uses three key strategies: (1) hierarchical modeling of subgroups within treatment arms that allows for borrowing of information across subgroups, (2) utilization of response-adaptive randomization (RAR) schemes that seek a tradeoff between statistical power and patient benefit, and (3) adjustment for potential drift over time. Motivated by a proposed clinical trial that aims to find the appropriate treatment for different subgroup populations of ischemic stroke patients, extensive simulation studies were performed to validate the approach, compare different allocation rules, and study the model operating characteristics. RESULTS AND CONCLUSIONS: Our proposed approach achieved high statistical power and good patient benefit and was also robust against population drift over time. Our design provided a good balance between the strengths of both the traditional RAR scheme and fixed 1:1 allocation and may be a promising choice for dichotomous outcomes trials investigating multiple subgroups. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-022-06664-4.
format Online
Article
Text
id pubmed-9446515
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-94465152022-09-07 Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients Gao, Guangyi Gajewski, Byron J. Wick, Jo Beall, Jonathan Saver, Jeffrey L. Meinzer, Caitlyn Trials Methodology BACKGROUND: Platform trials are well-known for their ability to investigate multiple arms on heterogeneous patient populations and their flexibility to add/drop treatment arms due to efficacy/lack of efficacy. Because of their complexity, it is important to develop highly optimized, transparent, and rigorous designs that are cost-efficient, offer high statistical power, maximize patient benefit, and are robust to changes over time. METHODS: To address these needs, we present a Bayesian platform trial design based on a beta-binomial model for binary outcomes that uses three key strategies: (1) hierarchical modeling of subgroups within treatment arms that allows for borrowing of information across subgroups, (2) utilization of response-adaptive randomization (RAR) schemes that seek a tradeoff between statistical power and patient benefit, and (3) adjustment for potential drift over time. Motivated by a proposed clinical trial that aims to find the appropriate treatment for different subgroup populations of ischemic stroke patients, extensive simulation studies were performed to validate the approach, compare different allocation rules, and study the model operating characteristics. RESULTS AND CONCLUSIONS: Our proposed approach achieved high statistical power and good patient benefit and was also robust against population drift over time. Our design provided a good balance between the strengths of both the traditional RAR scheme and fixed 1:1 allocation and may be a promising choice for dichotomous outcomes trials investigating multiple subgroups. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-022-06664-4. BioMed Central 2022-09-06 /pmc/articles/PMC9446515/ /pubmed/36068547 http://dx.doi.org/10.1186/s13063-022-06664-4 Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Gao, Guangyi
Gajewski, Byron J.
Wick, Jo
Beall, Jonathan
Saver, Jeffrey L.
Meinzer, Caitlyn
Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients
title Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients
title_full Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients
title_fullStr Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients
title_full_unstemmed Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients
title_short Optimizing a Bayesian hierarchical adaptive platform trial design for stroke patients
title_sort optimizing a bayesian hierarchical adaptive platform trial design for stroke patients
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446515/
https://www.ncbi.nlm.nih.gov/pubmed/36068547
http://dx.doi.org/10.1186/s13063-022-06664-4
work_keys_str_mv AT gaoguangyi optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients
AT gajewskibyronj optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients
AT wickjo optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients
AT bealljonathan optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients
AT saverjeffreyl optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients
AT meinzercaitlyn optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients
AT optimizingabayesianhierarchicaladaptiveplatformtrialdesignforstrokepatients