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Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods

Umbrella trials are an innovative trial design where different treatments are matched with subtypes of a disease, with the matching typically based on a set of biomarkers. Consequently, when patients can be positive for more than one biomarker, they may be eligible for multiple treatment arms. In pr...

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Autores principales: Ouma, Luke Ondijo, Grayling, Michael J., Zheng, Haiyan, Wason, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612600/
https://www.ncbi.nlm.nih.gov/pubmed/33759353
http://dx.doi.org/10.1002/pst.2119
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author Ouma, Luke Ondijo
Grayling, Michael J.
Zheng, Haiyan
Wason, James
author_facet Ouma, Luke Ondijo
Grayling, Michael J.
Zheng, Haiyan
Wason, James
author_sort Ouma, Luke Ondijo
collection PubMed
description Umbrella trials are an innovative trial design where different treatments are matched with subtypes of a disease, with the matching typically based on a set of biomarkers. Consequently, when patients can be positive for more than one biomarker, they may be eligible for multiple treatment arms. In practice, different approaches could be applied to allocate patients who are positive for multiple biomarkers to treatments. However, to date there has been little exploration of how these approaches compare statistically. We conduct a simulation study to compare five approaches to handling treatment allocation in the presence of multiple biomarkers – equal randomisation; randomisation with fixed probability of allocation to control; Bayesian adaptive randomisation (BAR); constrained randomisation; and hierarchy of biomarkers. We evaluate these approaches under different scenarios in the context of a hypothetical phase II biomarker-guided umbrella trial. We define the pairings representing the pre-trial expectations on efficacy as linked pairs, and the other biomarker-treatment pairings as unlinked. The hierarchy and BAR approaches have the highest power to detect a treatment-biomarker linked interaction. However, the hierarchy procedure performs poorly if the pre-specified treatment-biomarker pairings are incorrect. The BAR method allocates a higher proportion of patients who are positive for multiple biomarkers to promising treatments when an unlinked interaction is present. In most scenarios, the constrained randomisation approach best balances allocation to all treatment arms. Pre-specification of an approach to deal with treatment allocation in the presence of multiple biomarkers is important, especially when overlapping subgroups are likely.
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spelling pubmed-76126002022-04-11 Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods Ouma, Luke Ondijo Grayling, Michael J. Zheng, Haiyan Wason, James Pharm Stat Article Umbrella trials are an innovative trial design where different treatments are matched with subtypes of a disease, with the matching typically based on a set of biomarkers. Consequently, when patients can be positive for more than one biomarker, they may be eligible for multiple treatment arms. In practice, different approaches could be applied to allocate patients who are positive for multiple biomarkers to treatments. However, to date there has been little exploration of how these approaches compare statistically. We conduct a simulation study to compare five approaches to handling treatment allocation in the presence of multiple biomarkers – equal randomisation; randomisation with fixed probability of allocation to control; Bayesian adaptive randomisation (BAR); constrained randomisation; and hierarchy of biomarkers. We evaluate these approaches under different scenarios in the context of a hypothetical phase II biomarker-guided umbrella trial. We define the pairings representing the pre-trial expectations on efficacy as linked pairs, and the other biomarker-treatment pairings as unlinked. The hierarchy and BAR approaches have the highest power to detect a treatment-biomarker linked interaction. However, the hierarchy procedure performs poorly if the pre-specified treatment-biomarker pairings are incorrect. The BAR method allocates a higher proportion of patients who are positive for multiple biomarkers to promising treatments when an unlinked interaction is present. In most scenarios, the constrained randomisation approach best balances allocation to all treatment arms. Pre-specification of an approach to deal with treatment allocation in the presence of multiple biomarkers is important, especially when overlapping subgroups are likely. 2021-11-01 2021-03-24 /pmc/articles/PMC7612600/ /pubmed/33759353 http://dx.doi.org/10.1002/pst.2119 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Ouma, Luke Ondijo
Grayling, Michael J.
Zheng, Haiyan
Wason, James
Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods
title Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods
title_full Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods
title_fullStr Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods
title_full_unstemmed Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods
title_short Treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: A comparison of methods
title_sort treatment allocation strategies for umbrella trials in the presence of multiple biomarkers: a comparison of methods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612600/
https://www.ncbi.nlm.nih.gov/pubmed/33759353
http://dx.doi.org/10.1002/pst.2119
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