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Optimized adaptive enrichment designs
Based on a Bayesian decision theoretic approach, we optimize frequentist single- and adaptive two-stage trial designs for the development of targeted therapies, where in addition to an overall population, a pre-defined subgroup is investigated. In such settings, the losses and gains of decisions can...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613177/ https://www.ncbi.nlm.nih.gov/pubmed/29254436 http://dx.doi.org/10.1177/0962280217747312 |
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author | Ondra, Thomas Jobjörnsson, Sebastian Beckman, Robert A Burman, Carl-Fredrik König, Franz Stallard, Nigel Posch, Martin |
author_facet | Ondra, Thomas Jobjörnsson, Sebastian Beckman, Robert A Burman, Carl-Fredrik König, Franz Stallard, Nigel Posch, Martin |
author_sort | Ondra, Thomas |
collection | PubMed |
description | Based on a Bayesian decision theoretic approach, we optimize frequentist single- and adaptive two-stage trial designs for the development of targeted therapies, where in addition to an overall population, a pre-defined subgroup is investigated. In such settings, the losses and gains of decisions can be quantified by utility functions that account for the preferences of different stakeholders. In particular, we optimize expected utilities from the perspectives both of a commercial sponsor, maximizing the net present value, and also of the society, maximizing cost-adjusted expected health benefits of a new treatment for a specific population. We consider single-stage and adaptive two-stage designs with partial enrichment, where the proportion of patients recruited from the subgroup is a design parameter. For the adaptive designs, we use a dynamic programming approach to derive optimal adaptation rules. The proposed designs are compared to trials which are non-enriched (i.e. the proportion of patients in the subgroup corresponds to the prevalence in the underlying population). We show that partial enrichment designs can substantially improve the expected utilities. Furthermore, adaptive partial enrichment designs are more robust than single-stage designs and retain high expected utilities even if the expected utilities are evaluated under a different prior than the one used in the optimization. In addition, we find that trials optimized for the sponsor utility function have smaller sample sizes compared to trials optimized under the societal view and may include the overall population (with patients from the complement of the subgroup) even if there is substantial evidence that the therapy is only effective in the subgroup. |
format | Online Article Text |
id | pubmed-6613177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-66131772019-07-24 Optimized adaptive enrichment designs Ondra, Thomas Jobjörnsson, Sebastian Beckman, Robert A Burman, Carl-Fredrik König, Franz Stallard, Nigel Posch, Martin Stat Methods Med Res Articles Based on a Bayesian decision theoretic approach, we optimize frequentist single- and adaptive two-stage trial designs for the development of targeted therapies, where in addition to an overall population, a pre-defined subgroup is investigated. In such settings, the losses and gains of decisions can be quantified by utility functions that account for the preferences of different stakeholders. In particular, we optimize expected utilities from the perspectives both of a commercial sponsor, maximizing the net present value, and also of the society, maximizing cost-adjusted expected health benefits of a new treatment for a specific population. We consider single-stage and adaptive two-stage designs with partial enrichment, where the proportion of patients recruited from the subgroup is a design parameter. For the adaptive designs, we use a dynamic programming approach to derive optimal adaptation rules. The proposed designs are compared to trials which are non-enriched (i.e. the proportion of patients in the subgroup corresponds to the prevalence in the underlying population). We show that partial enrichment designs can substantially improve the expected utilities. Furthermore, adaptive partial enrichment designs are more robust than single-stage designs and retain high expected utilities even if the expected utilities are evaluated under a different prior than the one used in the optimization. In addition, we find that trials optimized for the sponsor utility function have smaller sample sizes compared to trials optimized under the societal view and may include the overall population (with patients from the complement of the subgroup) even if there is substantial evidence that the therapy is only effective in the subgroup. SAGE Publications 2017-12-18 2019-07 /pmc/articles/PMC6613177/ /pubmed/29254436 http://dx.doi.org/10.1177/0962280217747312 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Articles Ondra, Thomas Jobjörnsson, Sebastian Beckman, Robert A Burman, Carl-Fredrik König, Franz Stallard, Nigel Posch, Martin Optimized adaptive enrichment designs |
title | Optimized adaptive enrichment designs |
title_full | Optimized adaptive enrichment designs |
title_fullStr | Optimized adaptive enrichment designs |
title_full_unstemmed | Optimized adaptive enrichment designs |
title_short | Optimized adaptive enrichment designs |
title_sort | optimized adaptive enrichment designs |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613177/ https://www.ncbi.nlm.nih.gov/pubmed/29254436 http://dx.doi.org/10.1177/0962280217747312 |
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