Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials

Pharmacogenetics and biomarkers are becoming normalised as important technologies to improve drug efficacy rates, reduce the incidence of adverse drug reactions, and make informed choices for targeted therapies. However, their wider clinical implementation has been limited by a lack of robust eviden...

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Main Authors: Danielle Johnson, Dyfrig Hughes, Munir Pirmohamed, Andrea Jorgensen
Format: Article
Language:English
Published: MDPI AG 2019-09-01
Series:Journal of Personalized Medicine
Subjects:
RCT
Online Access:https://www.mdpi.com/2075-4426/9/3/42
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spelling doaj-dc0c087d0fe44291a82da9d1d1eaade72020-11-25T02:44:23ZengMDPI AGJournal of Personalized Medicine2075-44262019-09-01934210.3390/jpm9030042jpm9030042Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled TrialsDanielle Johnson0Dyfrig Hughes1Munir Pirmohamed2Andrea Jorgensen3Institute of Translational Medicine, Department of Biostatistics, University of Liverpool, Waterhouse Building, 1-5 Brownlow Street, Liverpool L69 3GL, UKCentre for Health Economics and Medicines Evaluation, Bangor University, Ardudwy, Normal Site, Bangor LL57 2PZ, UKMRC Centre for Drug Safety Science and Wolfson Centre for Personalised Medicine, Institute of Translational Medicine, Waterhouse Building, 1-5 Brownlow Street, Liverpool L69 3GL, UKInstitute of Translational Medicine, Department of Biostatistics, University of Liverpool, Waterhouse Building, 1-5 Brownlow Street, Liverpool L69 3GL, UKPharmacogenetics and biomarkers are becoming normalised as important technologies to improve drug efficacy rates, reduce the incidence of adverse drug reactions, and make informed choices for targeted therapies. However, their wider clinical implementation has been limited by a lack of robust evidence. Suitable evidence is required before a biomarker’s clinical use, and also before its use in a clinical trial. We have undertaken a review of five pharmacogenetic biomarker-guided randomised controlled trials (RCTs) and evaluated the evidence used by these trials to justify biomarker inclusion. We assessed and quantified the evidence cited in published rationale papers, or where these were not available, obtained protocols from trial authors. Very different levels of evidence were provided by the trials. We used these observations to write recommendations for future justifications of biomarker use in RCTs and encourage regulatory authorities to write clear guidelines.https://www.mdpi.com/2075-4426/9/3/42pharmacogeneticsbiomarkeradverse drug reactionsRCTevidence
collection DOAJ
language English
format Article
sources DOAJ
author Danielle Johnson
Dyfrig Hughes
Munir Pirmohamed
Andrea Jorgensen
spellingShingle Danielle Johnson
Dyfrig Hughes
Munir Pirmohamed
Andrea Jorgensen
Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
Journal of Personalized Medicine
pharmacogenetics
biomarker
adverse drug reactions
RCT
evidence
author_facet Danielle Johnson
Dyfrig Hughes
Munir Pirmohamed
Andrea Jorgensen
author_sort Danielle Johnson
title Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
title_short Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
title_full Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
title_fullStr Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
title_full_unstemmed Evidence to Support Inclusion of Pharmacogenetic Biomarkers in Randomised Controlled Trials
title_sort evidence to support inclusion of pharmacogenetic biomarkers in randomised controlled trials
publisher MDPI AG
series Journal of Personalized Medicine
issn 2075-4426
publishDate 2019-09-01
description Pharmacogenetics and biomarkers are becoming normalised as important technologies to improve drug efficacy rates, reduce the incidence of adverse drug reactions, and make informed choices for targeted therapies. However, their wider clinical implementation has been limited by a lack of robust evidence. Suitable evidence is required before a biomarker’s clinical use, and also before its use in a clinical trial. We have undertaken a review of five pharmacogenetic biomarker-guided randomised controlled trials (RCTs) and evaluated the evidence used by these trials to justify biomarker inclusion. We assessed and quantified the evidence cited in published rationale papers, or where these were not available, obtained protocols from trial authors. Very different levels of evidence were provided by the trials. We used these observations to write recommendations for future justifications of biomarker use in RCTs and encourage regulatory authorities to write clear guidelines.
topic pharmacogenetics
biomarker
adverse drug reactions
RCT
evidence
url https://www.mdpi.com/2075-4426/9/3/42
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