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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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 |
work_keys_str_mv |
AT daniellejohnson evidencetosupportinclusionofpharmacogeneticbiomarkersinrandomisedcontrolledtrials AT dyfrighughes evidencetosupportinclusionofpharmacogeneticbiomarkersinrandomisedcontrolledtrials AT munirpirmohamed evidencetosupportinclusionofpharmacogeneticbiomarkersinrandomisedcontrolledtrials AT andreajorgensen evidencetosupportinclusionofpharmacogeneticbiomarkersinrandomisedcontrolledtrials |
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