Publication: Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study.
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Identifiers
Date
2020/03/02
Authors
van der Wouden, Cathelijne H
Bohringer, Stefan
Cecchin, Erika
Cheung, Ka-Chun
Davila-Fajardo, Cristina Lucía
Deneer, Vera H M
Dolžan, Vita
Ingelman-Sundberg, Magnus
Jonsson, Siv
Karlsson, Mats O
Advisors
Journal Title
Journal ISSN
Volume Title
Publisher
Lippincott Williams & Wilkins
Abstract
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. 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. 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. 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.
Description
MeSH Terms
Drug-Related Side Effects and Adverse Reactions
Evidence-Based Medicine
Humans
Models, Statistical
Pharmacogenomic Testing
Practice Guidelines as Topic
Precision Medicine
Prospective Studies
Evidence-Based Medicine
Humans
Models, Statistical
Pharmacogenomic Testing
Practice Guidelines as Topic
Precision Medicine
Prospective Studies
DeCS Terms
Farmacogenómica
Efectos Colaterales y Reacciones Adversas
Medicina de Precisión
Pruebas de farmacogenómica
Medicina basada en la evidencia
Efectos Colaterales y Reacciones Adversas
Medicina de Precisión
Pruebas de farmacogenómica
Medicina basada en la evidencia
CIE Terms
Keywords
Citation
van der Wouden CH, Böhringer S, Cecchin E, Cheung KC, Dávila-Fajardo CL, Deneer VHM, eta al, Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study. Pharmacogenet Genomics. 2020 Aug;30(6):131-144.