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Clin Pharmacol Drug Dev. 2024 Jun;13(6):644-654. doi: 10.1002/cpdd.1406. Epub 2024 May 6.
2
Effect of letermovir initiation on tacrolimus concentrations among lung transplant recipients receiving concomitant azole antifungal prophylaxis.来氟米特起始治疗对同时接受唑类抗真菌预防治疗的肺移植受者他克莫司浓度的影响。
Transpl Infect Dis. 2024 Apr;26(2):e14267. doi: 10.1111/tid.14267. Epub 2024 Mar 15.
3
Physiologically Based Pharmacokinetic Modeling for Maribavir to Inform Dosing in Drug-Drug Interaction Scenarios with CYP3A4 Inducers and Inhibitors.基于生理的马拉维若药代动力学模型用于指导与 CYP3A4 诱导剂和抑制剂的药物相互作用情况下的剂量调整。
J Clin Pharmacol. 2024 May;64(5):590-600. doi: 10.1002/jcph.2385. Epub 2023 Dec 14.
4
Drug interactions of tacrolimus with letermovir and azole antifungals following hematopoietic stem cell transplantation: A retrospective observational analysis.他克莫司与来特莫韦和唑类抗真菌药在造血干细胞移植后的药物相互作用:一项回顾性观察性分析。
Pharmacol Res Perspect. 2023 Aug;11(4):e01120. doi: 10.1002/prp2.1120.
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What the Product Label Does Not Tell You About Drug-Drug Interaction Management: Time for a Re-Appraisal.药品标签未告知您的药物相互作用管理知识:是时候重新评估了。
J Clin Pharmacol. 2023 Nov;63(11):1181-1185. doi: 10.1002/jcph.2316. Epub 2023 Aug 1.
6
Letermovir vs Valganciclovir for Prophylaxis of Cytomegalovirus in High-Risk Kidney Transplant Recipients: A Randomized Clinical Trial.来特莫韦与缬更昔洛韦预防高危肾移植受者巨细胞病毒感染:一项随机临床试验。
JAMA. 2023 Jul 3;330(1):33-42. doi: 10.1001/jama.2023.9106.
7
Developing a mechanistic understanding of the nonlinear pharmacokinetics of letermovir and prospective drug interaction with everolimus using physiological-based pharmacokinetic modeling.应用生理药代动力学模型探究来特莫韦非线性药代动力学的机制并预测与依维莫司的药物相互作用。
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Evaluation of the inhibitory effects of itraconazole on letermovir.评估伊曲康唑对乐韦莫及的抑制作用。
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10
Voriconazole in Hematopoietic Stem Cell Transplantation and Cellular Therapies: Real-World Usage and Therapeutic Level Attainment at a Major Transplantation Center.伏立康唑在造血干细胞移植和细胞治疗中的应用:主要移植中心的真实世界使用情况和治疗水平达标情况。
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新型抗巨细胞病毒药物乐特韦和马拉韦罗的药物相互作用管理:临床医生指南。

Drug-Drug Interaction Management with the Novel Anti-Cytomegalovirus Agents Letermovir and Maribavir: Guidance for Clinicians.

机构信息

Department of Pharmacy, Radboudumc Institute for Medical Innovation (RIMI), Radboudumc, Geert Grooteplein 10, 6525 GA, Nijmegen, The Netherlands.

Global DDI Solutions, Utrecht, The Netherlands.

出版信息

Clin Pharmacokinet. 2024 Nov;63(11):1529-1546. doi: 10.1007/s40262-024-01437-5. Epub 2024 Nov 7.

DOI:10.1007/s40262-024-01437-5
PMID:39509076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11573823/
Abstract

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.

摘要

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。