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早期 boceprevir-S 对映体血浆浓度与 HCV 基因型 1 三联疗法突破发作之间的关系。

Relationship between the early boceprevir-S isomer plasma concentrations and the onset of breakthrough during HCV genotype 1 triple therapy.

机构信息

Department of Infectious Diseases, University of Turin, Amedeo di Savoia Hospital, Turin, Italy.

Department of Infectious Diseases, University of Turin, Amedeo di Savoia Hospital, Turin, Italy.

出版信息

Clin Microbiol Infect. 2015 Feb;21(2):205.e1-3. doi: 10.1016/j.cmi.2014.07.009. Epub 2014 Oct 29.

Abstract

In a prospective cohort of 18 patients treated with boceprevir, we examined the role of boceprevir plasma concentration at the onset of breakthrough during the treatment. Nine patients experienced breakthrough during therapy. The resistance patterns were as follows: S122S/R, I132V, T54A/I132V, V156S/I170A, V36M/T54S/R155K, V36M/R155K and T54/R155K. Boceprevir-S isomer (SCH 534128) median concentration in patients with breakthrough was 48.3 ng/mL (interquartile range 43-58 ng/mL); in others, it was significantly (p 0.019) higher: 151 ng/mL. Low boceprevir plasma concentration can lead to virologic resistance; therapeutic drug monitoring should be used to prevent the onset of viral breakthrough during triple-regimen therapy with boceprevir.

摘要

在一项前瞻性队列研究中,我们观察了 18 例接受博赛匹韦治疗的患者在治疗过程中发生突破性感染时的博赛匹韦血浆浓度。9 例患者在治疗过程中发生突破性感染。耐药模式如下:S122S/R、I132V、T54A/I132V、V156S/I170A、V36M/T54S/R155K、V36M/R155K 和 T54/R155K。突破性感染患者的博赛匹韦-S 异构体(SCH 534128)中位数浓度为 48.3ng/mL(四分位间距为 43-58ng/mL);而在其他患者中,浓度显著更高(p0.019):151ng/mL。低博赛匹韦血浆浓度可能导致病毒耐药性;在博赛匹韦三联治疗中,应进行治疗药物监测以防止病毒突破性感染的发生。

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