Publication:
Generating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study.

dc.contributor.authorvan der Wouden, Cathelijne H
dc.contributor.authorBohringer, Stefan
dc.contributor.authorCecchin, Erika
dc.contributor.authorCheung, Ka-Chun
dc.contributor.authorDavila-Fajardo, Cristina Lucía
dc.contributor.authorDeneer, Vera H M
dc.contributor.authorDolžan, Vita
dc.contributor.authorIngelman-Sundberg, Magnus
dc.contributor.authorJonsson, Siv
dc.contributor.authorKarlsson, Mats O
dc.contributor.authorKriek, Marjolein
dc.contributor.authorMitropoulou, Christina
dc.contributor.authorPatrinos, George P
dc.contributor.authorPirmohamed, Munir
dc.contributor.authorRial-Sebbag, Emmanuelle
dc.contributor.authorSamwald, Matthias
dc.contributor.authorSchwab, Matthias
dc.contributor.authorSteinberger, Daniela
dc.contributor.authorStingl, Julia
dc.contributor.authorSunder-Plassmann, Gere
dc.contributor.authorToffoli, Giuseppe
dc.contributor.authorTurner, Richard M
dc.contributor.authorvan Rhenen, Mandy H
dc.contributor.authorvan Zwet, Erik
dc.contributor.authorSwen, Jesse J
dc.contributor.authorGuchelaar, Henk-Jan
dc.contributor.authorUbiquitous Pharmacogenomics Consortium
dc.contributor.funderEuropean Community’s Horizon 2020 Programme
dc.date.accessioned2023-02-08T14:46:36Z
dc.date.available2023-02-08T14:46:36Z
dc.date.issued2020/03/02
dc.description.abstractPharmacogenetic 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.
dc.description.sponsorshipWe would like to thank the Scientific Advisory Board (Prof. Russ Altman, Prof. Michel Eichelbaum, David Haerry, Prof. Mark Ratain, Prof. Mary Relling, and Prof. Dan Roden) for their insights in the development of the study protocol and statistical analysis plan. The research leading to these results has received funding from the European Community’s Horizon 2020 Programme under grant agreement No. 668353 (Ubiquitous Pharmacogenomics). M.S. is in part supported by the Robert Bosch Stiftung, Stuttgart, Germany
dc.description.versionsi
dc.identifier.citationvan 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.
dc.identifier.doi10.1097/FPC.0000000000000405
dc.identifier.essn1744-6880
dc.identifier.pmcPMC7331826
dc.identifier.pmid32317559
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331826/pdf
dc.identifier.unpaywallURLhttps://journals.lww.com/jpharmacogenetics/Fulltext/2020/08000/Generating_evidence_for_precision_medicine_.3.aspx
dc.identifier.urihttp://hdl.handle.net/10668/15406
dc.issue.number6
dc.journal.titlePharmacogenetics and genomics
dc.journal.titleabbreviationPharmacogenet Genomics
dc.language.isoen
dc.organizationHospital Universitario San Cecilio
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.page.number131-144
dc.publisherLippincott Williams & Wilkins
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectID668353
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.decsFarmacogenómica
dc.subject.decsEfectos Colaterales y Reacciones Adversas
dc.subject.decsMedicina de Precisión
dc.subject.decsPruebas de farmacogenómica
dc.subject.decsMedicina basada en la evidencia
dc.subject.meshDrug-Related Side Effects and Adverse Reactions
dc.subject.meshEvidence-Based Medicine
dc.subject.meshHumans
dc.subject.meshModels, Statistical
dc.subject.meshPharmacogenomic Testing
dc.subject.meshPractice Guidelines as Topic
dc.subject.meshPrecision Medicine
dc.subject.meshProspective Studies
dc.titleGenerating evidence for precision medicine: considerations made by the Ubiquitous Pharmacogenomics Consortium when designing and operationalizing the PREPARE study.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number30
dspace.entity.typePublication

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