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艾尔巴韦格拉瑞韦在成年患者和老年患者中的真实世界应用:PITER 队列中合并用药的前瞻性评估。

Real-life use of elbasvir/grazoprevir in adults and elderly patients: a prospective evaluation of comedications used in the PITER cohort.

机构信息

Center for Global Health, Istituto Superiore di Sanità, Rome, Italy.

Department of Hepatology, Gragnano Hospital, Naples, Italy.

出版信息

Antivir Ther. 2020;25(2):73-81. doi: 10.3851/IMP3350.

Abstract

BACKGROUND

In patients treated for HCV infection, potential drug-drug interactions (DDIs) can occur among direct-acting antiviral drugs (DAAs) and comedications used. The real-life effectiveness and safety of elbasvir/grazoprevir (ELB/GZR) among co-medicated HCV patients was evaluated.

METHODS

We prospectively evaluated consecutive patients from 15 clinical centres participating in PITER who were treated with ELB/GZR and had been followed for at least 12 weeks after treatment. Data were prospectively collected on the use of comedications (including discontinuation, dose modification and addition of drugs) and potential DDIs with DAAs.

RESULTS

Of the 356 patients with at least 12-week post-treatment follow-up (median age 67, range 50-88 years), 338 (95%) achieved sustained virological response. Of these, 219 (60%) had at least one comorbidity (median 2, range 1-6); information on comedication was available for 212 of them. Of 190 comedications used, 15 (8%) drugs were modified during ELB/GZR therapy, specifically in 9 (4%) patients they were interrupted, in 2 (1%) of whom, the comedication was interrupted before the DAA therapy because of potential DDI (that is, patients treated with carbamazepine); in 12 (6%) patients the comedications were modified in terms of dosage. In 29 (14%) patients, the comedications required monitoring when used with ELB/GZR, as well as with all available DAAs. Of the 190 drugs, 27 (14%) used in 67% of patients were free of DDIs when used with ELB/GZR, whereas they required monitoring if used with other DAA regimens.

CONCLUSIONS

The results of this prospective study support findings that ELB/GZR is effective and safe in most treated patients.

摘要

背景

在接受 HCV 感染治疗的患者中,直接作用抗病毒药物(DAAs)和合并用药之间可能发生潜在的药物相互作用(DDI)。评估了 ELB/GZR 在合并用药的 HCV 患者中的真实有效性和安全性。

方法

我们前瞻性评估了来自参与 PITER 的 15 个临床中心的连续患者,这些患者接受了 ELB/GZR 治疗,并在治疗后至少随访 12 周。前瞻性收集了合并用药(包括停药、剂量调整和加药)和与 DAA 潜在 DDI 的数据。

结果

在至少有 12 周治疗后随访的 356 例患者中(中位年龄 67 岁,范围 50-88 岁),338 例(95%)获得持续病毒学应答。其中,219 例(60%)有至少一种合并症(中位 2 种,范围 1-6);他们中有 212 例的合并用药信息可用。190 种合并用药中,15 种(8%)药物在 ELB/GZR 治疗期间进行了调整,具体来说,9 种(4%)药物被中断,其中 2 种(1%)药物因潜在的 DDI(即接受卡马西平治疗的患者)在 DAA 治疗前中断了合并用药;12 种(6%)药物在剂量上进行了调整。在 29 例(14%)患者中,当与 ELB/GZR 一起使用时,以及与所有可用的 DAA 一起使用时,需要监测这些合并用药。在 190 种药物中,27 种(14%)药物在 67%的患者中使用时与 ELB/GZR 无 DDI,但如果与其他 DAA 方案一起使用则需要监测。

结论

这项前瞻性研究的结果支持 ELB/GZR 在大多数接受治疗的患者中有效且安全的发现。

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