新型抗巨细胞病毒药物 Letermovir 和 Maribavir 的药物相互作用管理:临床医师指南》。

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY Clinical Pharmacokinetics Pub Date : 2024-11-01 Epub Date: 2024-11-07 DOI:10.1007/s40262-024-01437-5
David M Burger, Laura Nijboer, Mira Ghobreyal, Johan Maertens, Nicole Blijlevens, Luuk Hilbrands, Marije C Baas, Per Ljungman, Roger J M Brüggemann
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引用次数: 0

摘要

来替莫韦和马立巴韦已分别证明可有效预防和治疗巨细胞病毒(CMV)感染和疾病的免疫抑制患者。这些患者通常需要同时服用多种药物,因此存在药物间相互作用的风险。来替莫韦和马立巴韦既可能是药物相互作用的肇事者,也可能是受害者。来替莫韦是 CYP3A、CYP2C8 和 OATP1B1/3 的中度抑制剂,也是 CYP2C19 的中度诱导剂。它是 UGT1A1/3、BCRP、P-gp 和 OATP1B1/3 的底物。马利巴韦是一种中度的 CYP2C9 抑制剂,也是 CYP3A 的底物。这些抗 CMV 药物与许多治疗类别(如免疫抑制剂、抗真菌剂和血液肿瘤药物)之间的药物相互作用可能会产生临床后果,因此需要调整剂量或密切监测。在一些例子中,需要对三方药物相互作用进行评估。本综述的目的是根据现有的药物相互作用研究数据为临床医生提供药物相互作用管理指南,并将其推及尚未研究但在这些患者群体中经常使用的其他相关联合用药。
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Drug-Drug Interaction Management with the Novel Anti-Cytomegalovirus Agents Letermovir and Maribavir: Guidance for Clinicians.

Letermovir and maribavir have demonstrated efficacy in the prevention and treatment, respectively, of immunosuppressed patients with cytomegalovirus (CMV) infection and disease. These patients often have polypharmacy making them at risk for drug-drug interactions. Both letermovir and maribavir can be perpetrators and victims of drug-drug interactions. Letermovir is a moderate inhibitor of CYP3A, CYP2C8 and OATP1B1/3, and a moderate inducer of CYP2C19. It is a substrate of UGT1A1/3, BCRP, P-gp and OATP1B1/3. Maribavir is a moderate CYP2C9 inhibitor and a substrate of CYP3A. Drug-drug interactions between these anti-CMV agents and a number of therapeutic classes, such as immunosuppressants, antifungal agents, and hemato-oncological agents, can have clinical consequences and deserve dose modification or close monitoring. In a number of examples, three-way drug interactions need to be assessed. The objective of this review is to provide clinicians with guidance for drug-drug interaction management, based on existing data from drug-drug interaction studies, and extrapolation to other relevant co-medications that have not (yet) been studied but that are frequently used in these patient populations.

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来源期刊
CiteScore
8.80
自引率
4.40%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Clinical Pharmacokinetics promotes the continuing development of clinical pharmacokinetics and pharmacodynamics for the improvement of drug therapy, and for furthering postgraduate education in clinical pharmacology and therapeutics. Pharmacokinetics, the study of drug disposition in the body, is an integral part of drug development and rational use. Knowledge and application of pharmacokinetic principles leads to accelerated drug development, cost effective drug use and a reduced frequency of adverse effects and drug interactions.
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