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Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study
Pharmacogenetic panel-based testing represents a new model for precision medicine. A sufficiently powered prospective study assessing the (cost-)effectiveness of a panel-based pharmacogenomics approach to guide pharmacotherapy is lacking. Therefore, the Ubiquitous Pharmacogenomics Consortium initiat...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331826/ https://www.ncbi.nlm.nih.gov/pubmed/32317559 http://dx.doi.org/10.1097/FPC.0000000000000405 |
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author | van der Wouden, Cathelijne H. Böhringer, Stefan Cecchin, Erika Cheung, Ka-Chun Dávila-Fajardo, Cristina Lucía Deneer, Vera H.M. Dolžan, Vita Ingelman-Sundberg, Magnus Jönsson, Siv Karlsson, Mats O. Kriek, Marjolein Mitropoulou, Christina Patrinos, George P. Pirmohamed, Munir Rial-Sebbag, Emmanuelle Samwald, Matthias Schwab, Matthias Steinberger, Daniela Stingl, Julia Sunder-Plassmann, Gere Toffoli, Giuseppe Turner, Richard M. van Rhenen, Mandy H. van Zwet, Erik Swen, Jesse J. Guchelaar, Henk-Jan |
author_facet | van der Wouden, Cathelijne H. Böhringer, Stefan Cecchin, Erika Cheung, Ka-Chun Dávila-Fajardo, Cristina Lucía Deneer, Vera H.M. Dolžan, Vita Ingelman-Sundberg, Magnus Jönsson, Siv Karlsson, Mats O. Kriek, Marjolein Mitropoulou, Christina Patrinos, George P. Pirmohamed, Munir Rial-Sebbag, Emmanuelle Samwald, Matthias Schwab, Matthias Steinberger, Daniela Stingl, Julia Sunder-Plassmann, Gere Toffoli, Giuseppe Turner, Richard M. van Rhenen, Mandy H. van Zwet, Erik Swen, Jesse J. Guchelaar, Henk-Jan |
author_sort | van der Wouden, Cathelijne H. |
collection | PubMed |
description | Pharmacogenetic panel-based testing represents a new model for precision medicine. A sufficiently powered prospective study assessing the (cost-)effectiveness of a panel-based pharmacogenomics approach to guide pharmacotherapy is lacking. Therefore, the Ubiquitous Pharmacogenomics Consortium initiated the PREemptive Pharmacogenomic testing for prevention of Adverse drug Reactions (PREPARE) study. Here, we provide an overview of considerations made to mitigate multiple methodological challenges that emerged during the design. METHODS: An evaluation of considerations made when designing the PREPARE study across six domains: study aims and design, primary endpoint definition and collection of adverse drug events, inclusion and exclusion criteria, target population, pharmacogenomics intervention strategy, and statistical analyses. RESULTS: Challenges and respective solutions included: (1) defining and operationalizing a composite primary endpoint enabling measurement of the anticipated effect, by including only severe, causal, and drug genotype-associated adverse drug reactions; (2) avoiding overrepresentation of frequently prescribed drugs within the patient sample while maintaining external validity, by capping drugs of enrolment; (3) designing the pharmacogenomics intervention strategy to be applicable across ethnicities and healthcare settings; and (4) designing a statistical analysis plan to avoid dilution of effect by initially excluding patients without a gene–drug interaction in a gatekeeping analysis. CONCLUSION: Our design considerations will enable quantification of the collective clinical utility of a panel of pharmacogenomics-markers within one trial as a proof-of-concept for pharmacogenomics-guided pharmacotherapy across multiple actionable gene–drug interactions. These considerations may prove useful to other investigators aiming to generate evidence for precision medicine. |
format | Online Article Text |
id | pubmed-7331826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-73318262020-07-13 Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study van der Wouden, Cathelijne H. Böhringer, Stefan Cecchin, Erika Cheung, Ka-Chun Dávila-Fajardo, Cristina Lucía Deneer, Vera H.M. Dolžan, Vita Ingelman-Sundberg, Magnus Jönsson, Siv Karlsson, Mats O. Kriek, Marjolein Mitropoulou, Christina Patrinos, George P. Pirmohamed, Munir Rial-Sebbag, Emmanuelle Samwald, Matthias Schwab, Matthias Steinberger, Daniela Stingl, Julia Sunder-Plassmann, Gere Toffoli, Giuseppe Turner, Richard M. van Rhenen, Mandy H. van Zwet, Erik Swen, Jesse J. Guchelaar, Henk-Jan Pharmacogenet Genomics Original Articles Pharmacogenetic panel-based testing represents a new model for precision medicine. A sufficiently powered prospective study assessing the (cost-)effectiveness of a panel-based pharmacogenomics approach to guide pharmacotherapy is lacking. Therefore, the Ubiquitous Pharmacogenomics Consortium initiated the PREemptive Pharmacogenomic testing for prevention of Adverse drug Reactions (PREPARE) study. Here, we provide an overview of considerations made to mitigate multiple methodological challenges that emerged during the design. METHODS: An evaluation of considerations made when designing the PREPARE study across six domains: study aims and design, primary endpoint definition and collection of adverse drug events, inclusion and exclusion criteria, target population, pharmacogenomics intervention strategy, and statistical analyses. RESULTS: Challenges and respective solutions included: (1) defining and operationalizing a composite primary endpoint enabling measurement of the anticipated effect, by including only severe, causal, and drug genotype-associated adverse drug reactions; (2) avoiding overrepresentation of frequently prescribed drugs within the patient sample while maintaining external validity, by capping drugs of enrolment; (3) designing the pharmacogenomics intervention strategy to be applicable across ethnicities and healthcare settings; and (4) designing a statistical analysis plan to avoid dilution of effect by initially excluding patients without a gene–drug interaction in a gatekeeping analysis. CONCLUSION: Our design considerations will enable quantification of the collective clinical utility of a panel of pharmacogenomics-markers within one trial as a proof-of-concept for pharmacogenomics-guided pharmacotherapy across multiple actionable gene–drug interactions. These considerations may prove useful to other investigators aiming to generate evidence for precision medicine. Lippincott Williams & Wilkins 2020-04-20 2020-08 /pmc/articles/PMC7331826/ /pubmed/32317559 http://dx.doi.org/10.1097/FPC.0000000000000405 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) (CC-BY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Articles van der Wouden, Cathelijne H. Böhringer, Stefan Cecchin, Erika Cheung, Ka-Chun Dávila-Fajardo, Cristina Lucía Deneer, Vera H.M. Dolžan, Vita Ingelman-Sundberg, Magnus Jönsson, Siv Karlsson, Mats O. Kriek, Marjolein Mitropoulou, Christina Patrinos, George P. Pirmohamed, Munir Rial-Sebbag, Emmanuelle Samwald, Matthias Schwab, Matthias Steinberger, Daniela Stingl, Julia Sunder-Plassmann, Gere Toffoli, Giuseppe Turner, Richard M. van Rhenen, Mandy H. van Zwet, Erik Swen, Jesse J. Guchelaar, Henk-Jan Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study |
title | Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study |
title_full | Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study |
title_fullStr | Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study |
title_full_unstemmed | Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study |
title_short | Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study |
title_sort | generating evidence for precision medicine: considerations made by the ubiquitous pharmacogenomics consortium when designing and operationalizing the prepare study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331826/ https://www.ncbi.nlm.nih.gov/pubmed/32317559 http://dx.doi.org/10.1097/FPC.0000000000000405 |
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