| Literature DB >> 27143031 |
J Kevin Hicks1,2, Blanca E Gonzalez3, Anthony S Zembillas1, Karissa Kusick1, Sudish Murthy4, Siva Raja4, Steven M Gordon3, Rabi Hanna5.
Abstract
Individuals who carry the CYP2C19*17 gain-of-function allele have lower voriconazole exposure and are therefore at risk of failing therapy. Utilizing CYP2C19 genotype to optimize voriconazole dosage may be a cost-effective method of improving treatment outcomes. However, there are limited data describing what initial voriconazole dosage should be used in those with increased CYP2C19 metabolic capacity. Herein, we present a case report of a pediatric CYP2C19 rapid metabolizer (i.e., CYP2C19*1/*17) requiring a voriconazole dosage of 14 mg/kg twice daily (usual pediatric dosage ranges from 7 to 9 mg/kg twice daily). This case report supports the clinical utility of using CYP2C19 genotype to guide voriconazole dosing, and provides data for establishing an initial voriconazole dose in pediatric CYP2C19 rapid metabolizers.Entities:
Keywords: CYP2C19; personalized medicine; pharmacogenomics; precision medicine; therapeutic drug monitoring; voriconazole
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Year: 2016 PMID: 27143031 DOI: 10.2217/pgs-2015-0014
Source DB: PubMed Journal: Pharmacogenomics ISSN: 1462-2416 Impact factor: 2.533