French-Speaking Network of Pharmacogenetics (RNPGx) Recommendations for Clinical Use of Mavacamten.

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Louis Lebreton, Jean-Christophe Boyer, Claire Lafay-Chebassier, Benjamin Hennart, Sarah Baklouti, Séverine Cunat, Paul Vilquin, Yves Medard, Elodie Gautier-Veyret, Clara Laffitte-Redondo, Céline Verstuyft, Abd El Kader Ait Tayeb, Vincent Haufroid, Julien Wils, Fabien Lamoureux, Alexandre Evrard, Julie Davaze-Schneider, Mouna Ben-Sassi, Nicolas Picard, Sylvie Quaranta, Estelle Ayme-Dietrich
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引用次数: 0

Abstract

Mavacamten, the first drug in the class of β-cardiac myosin modulator, is used for the treatment of patients with hypertrophic cardiomyopathy. This orally administered drug demonstrates wide interpatient variability in pharmacokinetics parameters, due in part to variant CYP2C19 alleles. Individuals who are CYP2C19 poor metabolizers have increased exposure and are at increased risk of reduced cardiac hypercontractility. To ensure the safety of all patients, European Medicines Agency recommends CYP2C19 preemptive genotyping, and consecutively, to adapt maintenance and initial mavacamten doses, and to manage drug-drug interactions, according to CYP2C19 phenotype. In this article, we summarize evidence from the literature supporting the association between CYP2C19 phenotype and pharmacological features of mavacamten and provide, beyond biologic guidelines, therapeutic recommendations for the use of mavacamten based on CYP2C19 and CYP3A4/CYP3A5 genotype.

法语国家药物遗传学网络 (RNPGx) 对 Mavacamten 临床使用的建议。
Mavacamten是β-心肌酶调节剂中的第一种药物,用于治疗肥厚型心肌病患者。这种口服药物的药代动力学参数在患者之间存在很大差异,部分原因是 CYP2C19 等位基因的变异。CYP2C19 代谢较差的患者暴露量会增加,心脏收缩力减弱的风险也会增加。为确保所有患者的安全,欧洲药品管理局建议对 CYP2C19 进行先期基因分型,并根据 CYP2C19 表型连续调整马伐康坦的维持剂量和初始剂量,以及管理药物间的相互作用。在本文中,我们总结了支持CYP2C19表型与马伐康坦药理特征之间关联的文献证据,并根据CYP2C19和CYP3A4/CYP3A5基因型提供了生物指南之外的马伐康坦使用治疗建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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