Department of Pharmacy, Radboudumc Institute for Medical Innovation (RIMI), Radboudumc, Geert Grooteplein 10, 6525 GA, Nijmegen, The Netherlands.
Global DDI Solutions, Utrecht, The Netherlands.
Clin Pharmacokinet. 2024 Nov;63(11):1529-1546. doi: 10.1007/s40262-024-01437-5. Epub 2024 Nov 7.
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.
洛韦西韦和马拉维若分别在预防和治疗免疫抑制患者的巨细胞病毒(CMV)感染和疾病方面显示出疗效。这些患者通常需要同时使用多种药物,这使他们面临药物相互作用的风险。洛韦西韦和马拉维若都可能是药物相互作用的“肇事者”和“受害者”。洛韦西韦是 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。马拉维若为中度 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、抗真菌药物和血液肿瘤学药物)之间的药物相互作用可能具有临床意义,需要调整剂量或密切监测。在许多情况下,需要评估三种药物相互作用。本综述的目的是根据药物相互作用研究中的现有数据,并推断出其他尚未(但经常)在这些患者群体中使用的相关合并药物,为临床医生提供药物相互作用管理的指导。