Role of letermovir therapeutic drug monitoring for cytomegalovirus prophylaxis in allogeneic hematopoietic stem cell transplantation recipients: a prospective study.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Yulan Qiu, Xiaoning Wang, Juan Ren, Yijing Zhang, Chuqi Bai, Sasa Hu, Taotao Wang, Jiaojiao Chen, Chuhui Wang, Pengcheng He, Yalin Dong
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Abstract

Purpose: The role of therapeutic drug monitoring (TDM) in allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients receiving letermovir has not yet been clarified. This study is to explore letermovir trough concentration (Cmin) correlation with its clinical efficacy and adverse events, and factors affecting its plasma concentrations.

Methods: A prospective, non-interventional study was performed in allo-HSCT recipients receiving letermovir prophylaxis. Plasma concentrations were determined using high-performance liquid chromatography-tandem mass spectrometry. Data analysis was performed using logistic regression, linear regression, and classification and regression tree (CART) models.

Results: 701 trough concentrations from 71 recipients were included, uncovering pronounced intra- and inter-individual variability in letermovir Cmin. During 24-week follow-up, CMV infection incidence was 16.4%. A significant correlation was identified between letermovir Cmin and its clinical efficacy, and the CART model showed an increased risk of CMV infection when Cmin ≤ 2731 ng/mL. However, no clear correlation was found between Cmin and adverse events. Gastrointestinal graft-versus-host disease, cyclosporine Cmin, gender, and concomitant medications, including mycophenolate mofetil, ondansetron, caspofungin, and methylprednisolone, may impact letermovir Cmin. Additionally, coadministration with cyclosporine injection significantly decreased median letermovir Cmin compared with cyclosporine capsules (2311 vs. 3386 ng/mL). Moreover, with the extension of time post-transplant, trough concentrations of both cyclosporine and letermovir significantly decreased.

Conclusion: TDM for letermovir may be beneficial in allo-HSCT recipients considering the variability in letermovir Cmin and its correlation with clinical efficacy. Moreover, drug interactions and the effects of changes in cyclosporine dosage forms or concentrations require careful monitoring for their effect on letermovir Cmin.

同种异体造血干细胞移植受者预防巨细胞病毒的利特莫韦治疗药物监测作用:一项前瞻性研究。
目的:治疗药物监测(TDM)在接受来特莫韦治疗的异基因造血干细胞移植(allo-HSCT)受者中的作用尚未明确。本研究旨在探讨来曲莫韦谷浓度(Cmin)与其临床疗效和不良反应的相关性,以及影响其血浆浓度的因素:这项前瞻性、非干预性研究针对接受来特莫韦预防治疗的allo-HSCT受者。采用高效液相色谱-串联质谱法测定血浆浓度。数据分析采用逻辑回归、线性回归和分类回归树(CART)模型:结果:共纳入了 71 名受试者的 701 个谷浓度,发现了来特莫韦 Cmin 在个体内和个体间的明显差异。随访 24 周期间,CMV 感染率为 16.4%。来特莫韦 Cmin 与临床疗效之间存在明显的相关性,CART 模型显示,当 Cmin ≤ 2731 纳克/毫升时,CMV 感染风险增加。然而,在 Cmin 与不良事件之间没有发现明确的相关性。胃肠道移植物抗宿主疾病、环孢素 Cmin、性别以及同时服用的药物(包括霉酚酸酯、昂丹司琼、卡泊芬净和甲基强的松龙)可能会影响利特莫韦 Cmin。此外,与环孢素胶囊相比,与环孢素注射液联合用药可显著降低来曲米韦 Cmin 中位数(2311 对 3386 纳克/毫升)。此外,随着移植后时间的延长,环孢素和来特莫韦的谷浓度均显著下降:结论:考虑到来特莫韦 Cmin 的变化及其与临床疗效的相关性,来特莫韦的 TDM 可能对异体 HSCT 受者有益。此外,药物相互作用以及环孢素剂型或浓度变化的影响也需要仔细监测,以了解其对来特莫韦 Cmin 的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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