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Bayesian modelling strategies for borrowing of information in randomised basket trials
Basket trials are an innovative precision medicine clinical trial design evaluating a single targeted therapy across multiple diseases that share a common characteristic. To date, most basket trials have been conducted in early‐phase oncology settings, for which several Bayesian methods permitting i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827857/ https://www.ncbi.nlm.nih.gov/pubmed/36636028 http://dx.doi.org/10.1111/rssc.12602 |
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author | Ouma, Luke O. Grayling, Michael J. Wason, James M. S. Zheng, Haiyan |
author_facet | Ouma, Luke O. Grayling, Michael J. Wason, James M. S. Zheng, Haiyan |
author_sort | Ouma, Luke O. |
collection | PubMed |
description | Basket trials are an innovative precision medicine clinical trial design evaluating a single targeted therapy across multiple diseases that share a common characteristic. To date, most basket trials have been conducted in early‐phase oncology settings, for which several Bayesian methods permitting information sharing across subtrials have been proposed. With the increasing interest of implementing randomised basket trials, information borrowing could be exploited in two ways; considering the commensurability of either the treatment effects or the outcomes specific to each of the treatment groups between the subtrials. In this article, we extend a previous analysis model based on distributional discrepancy for borrowing over the subtrial treatment effects (‘treatment effect borrowing’, TEB) to borrowing over the subtrial groupwise responses (‘treatment response borrowing’, TRB). Simulation results demonstrate that both modelling strategies provide substantial gains over an approach with no borrowing. TRB outperforms TEB especially when subtrial sample sizes are small on all operational characteristics, while the latter has considerable gains in performance over TRB when subtrial sample sizes are large, or the treatment effects and groupwise mean responses are noticeably heterogeneous across subtrials. Further, we notice that TRB, and TEB can potentially lead to different conclusions in the analysis of real data. |
format | Online Article Text |
id | pubmed-9827857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98278572023-01-10 Bayesian modelling strategies for borrowing of information in randomised basket trials Ouma, Luke O. Grayling, Michael J. Wason, James M. S. Zheng, Haiyan J R Stat Soc Ser C Appl Stat Original Articles Basket trials are an innovative precision medicine clinical trial design evaluating a single targeted therapy across multiple diseases that share a common characteristic. To date, most basket trials have been conducted in early‐phase oncology settings, for which several Bayesian methods permitting information sharing across subtrials have been proposed. With the increasing interest of implementing randomised basket trials, information borrowing could be exploited in two ways; considering the commensurability of either the treatment effects or the outcomes specific to each of the treatment groups between the subtrials. In this article, we extend a previous analysis model based on distributional discrepancy for borrowing over the subtrial treatment effects (‘treatment effect borrowing’, TEB) to borrowing over the subtrial groupwise responses (‘treatment response borrowing’, TRB). Simulation results demonstrate that both modelling strategies provide substantial gains over an approach with no borrowing. TRB outperforms TEB especially when subtrial sample sizes are small on all operational characteristics, while the latter has considerable gains in performance over TRB when subtrial sample sizes are large, or the treatment effects and groupwise mean responses are noticeably heterogeneous across subtrials. Further, we notice that TRB, and TEB can potentially lead to different conclusions in the analysis of real data. John Wiley and Sons Inc. 2022-10-28 2022-11 /pmc/articles/PMC9827857/ /pubmed/36636028 http://dx.doi.org/10.1111/rssc.12602 Text en © 2022 The Authors. Journal of the Royal Statistical Society: Series C (Applied Statistics) published by John Wiley & Sons Ltd on behalf of Royal Statistical Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (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 | Original Articles Ouma, Luke O. Grayling, Michael J. Wason, James M. S. Zheng, Haiyan Bayesian modelling strategies for borrowing of information in randomised basket trials |
title | Bayesian modelling strategies for borrowing of information in randomised basket trials |
title_full | Bayesian modelling strategies for borrowing of information in randomised basket trials |
title_fullStr | Bayesian modelling strategies for borrowing of information in randomised basket trials |
title_full_unstemmed | Bayesian modelling strategies for borrowing of information in randomised basket trials |
title_short | Bayesian modelling strategies for borrowing of information in randomised basket trials |
title_sort | bayesian modelling strategies for borrowing of information in randomised basket trials |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827857/ https://www.ncbi.nlm.nih.gov/pubmed/36636028 http://dx.doi.org/10.1111/rssc.12602 |
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