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异基因造血细胞移植后乐韦莫及伏立康唑的药物相互作用。

Drug interaction between letermovir and voriconazole after allogeneic hematopoietic cell transplantation.

机构信息

Department of Pharmacy, National Cancer Center Hospital, Tokyo, Japan.

Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

出版信息

Int J Hematol. 2021 Jun;113(6):872-876. doi: 10.1007/s12185-021-03105-x. Epub 2021 Mar 7.

Abstract

Letermovir has been approved for the prevention of cytomegalovirus (CMV) infection after allogeneic hematopoietic stem cell transplantation (HCT). Letermovir is a cytochrome P450 (CYP) 2C19 inducer. Voriconazole, which is a broad-spectrum triazole antifungal agent, is mainly metabolized by CYP2C19. Thus, voriconazole trough concentration may decrease due to the drug interaction between voriconazole and letermovir. This study aimed to clarify the effects of letermovir on voriconazole trough concentration in allogeneic HCT recipients. We retrospectively examined voriconazole trough concentration in 24 allogeneic HCT recipients who had letermovir for prevention of CMV infection. The median voriconazole C/D ratios significantly decreased after starting letermovir from 0.25 L/kg to 0.11 L/kg (p < 0.01), and increased after discontinuing letermovir from 0.15 L/kg to 0.24 L/kg (p = 0.02). The median fold change of voriconazole trough concentration during letermovir administration was 0.40. Our results suggest that voriconazole trough concentration decreases when voriconazole is combined with letermovir in allogeneic HCT recipients. Therefore, close therapeutic drug monitoring of voriconazole trough concentration is warranted in allogeneic HCT recipients after starting or discontinuing letermovir.

摘要

洛韦莫韦已被批准用于异基因造血干细胞移植(HCT)后预防巨细胞病毒(CMV)感染。洛韦莫韦是细胞色素 P450(CYP)2C19 诱导剂。伏立康唑是一种广谱三唑类抗真菌药物,主要通过 CYP2C19 代谢。因此,由于伏立康唑和洛韦莫韦之间的药物相互作用,伏立康唑谷浓度可能会降低。本研究旨在阐明洛韦莫韦对异基因 HCT 受者伏立康唑谷浓度的影响。我们回顾性检查了 24 例接受异基因 HCT 且接受洛韦莫韦预防 CMV 感染的患者的伏立康唑谷浓度。从 0.25 L/kg 开始使用洛韦莫韦后,伏立康唑 C/D 比值中位数显著降低至 0.11 L/kg(p<0.01),停用洛韦莫韦后从 0.15 L/kg 增加至 0.24 L/kg(p=0.02)。伏立康唑谷浓度在使用洛韦莫韦期间的中位数变化倍数为 0.40。我们的结果表明,在异基因 HCT 受者中,伏立康唑与洛韦莫韦联合使用时,伏立康唑谷浓度降低。因此,在开始或停用洛韦莫韦后,有必要对异基因 HCT 受者进行伏立康唑谷浓度的密切治疗药物监测。

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