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来特莫韦和马拉韦罗用于治疗和预防实体器官和造血干细胞移植受者的巨细胞病毒感染。

Letermovir and Maribavir for the Treatment and Prevention of Cytomegalovirus Infection in Solid Organ and Stem Cell Transplant Recipients.

机构信息

University of Utah, Department of Internal Medicine, Division of Infectious Diseases, Salt Lake City, Utah, USA.

University of Michigan, Department of Internal Medicine, Division of Infectious Diseases, Ann Arbor, Michigan, USA.

出版信息

Clin Infect Dis. 2021 Jul 1;73(1):156-160. doi: 10.1093/cid/ciaa1713.

Abstract

Until recently, available drugs for cytomegalovirus (CMV) prevention and treatment in transplant patients included (val)ganciclovir, foscarnet, and cidofovir. Use of these drugs is limited by toxicity and the development of resistance. The 2017 approval of letermovir for prevention of CMV after stem cell transplant marked the first approval of an anti-CMV agent since 2003. The role of letermovir in treatment of established CMV infection or disease remains largely unstudied, although early reports suggest that a low barrier to resistance will likely limit efficacy as primary therapy for patients with refractory or resistant disease. The investigational agent maribavir has shown promise as preemptive treatment; in patients with refractory or resistant disease the emergence of resistance while on treatment has been observed and ongoing studies will define efficacy in this population. Both agents have unique mechanisms of action limiting cross resistance, and neither exhibit myelotoxicity or nephrotoxicity.

摘要

直到最近,移植患者可用的巨细胞病毒 (CMV) 预防和治疗药物包括缬更昔洛韦、膦甲酸钠和更昔洛韦。这些药物的使用受到毒性和耐药性发展的限制。2017 年,来特莫韦被批准用于干细胞移植后的 CMV 预防,这标志着自 2003 年以来首次批准了一种抗 CMV 药物。来特莫韦在治疗已确诊的 CMV 感染或疾病中的作用在很大程度上仍未得到研究,尽管早期报告表明,低耐药屏障可能会限制其作为耐药或难治性疾病患者的主要治疗药物的疗效。研究药物马拉维若在预防性治疗方面显示出良好的效果;在耐药或难治性疾病患者中,在治疗过程中观察到耐药性的出现,正在进行的研究将确定该人群的疗效。这两种药物具有独特的作用机制,限制了交叉耐药性,且均无骨髓毒性或肾毒性。

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