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格拉瑞韦联合艾尔巴韦格拉瑞韦治疗 4/5 期重度慢性肾脏病合并 HCV 基因型 1 或 4 感染患者是安全有效的。

Grazoprevir plus elbasvir in HCV genotype-1 or -4 infected patients with stage 4/5 severe chronic kidney disease is safe and effective.

机构信息

Department of Internal Medicine and Digestive Diseases, CHU Purpan, UMR 152 Pharma Dev, IRD Toulouse 3 University, Toulouse, France.

Digestive Department, CHU, Caen, France.

出版信息

Kidney Int. 2018 Jul;94(1):206-213. doi: 10.1016/j.kint.2018.02.019. Epub 2018 May 5.

Abstract

Patients with advanced chronic kidney disease who receive direct-acting antiviral drugs require special consideration regarding comorbid conditions. Here we assessed the efficacy and safety of grazoprevir plus elbasvir in 93 patients infected with HCV genotype 1 or 4 and with advanced chronic kidney disease in a non-randomized, multicenter, nationwide observational survey. Twenty patients with HCV genotype 1a, 51 patients with 1b, four unclassified genotype 1, 17 with genotype 4 and one with genotype 6 received grazoprevir plus elbasvir (100/50 mg) once daily. All patients had severe chronic kidney disease with 70 patients stage G5, including patients on hemodialysis (74.2%), and 23 were stage G4 chronic kidney disease. Severe liver disease (Metavir F3/F4) was found in 33 patients. A sustained virologic response 12 weeks after the end of therapy was achieved in 87 of 90 patients. Two patients had a virologic breakthrough and one had a relapse after treatment withdrawal. Most patients received many concomitant medications (mean 7.7) related to comorbid conditions. Serious adverse events occurred in six patients, including three deaths while on grazoprevir plus elbasvir, not related to this therapy. Thus, once-daily grazoprevir plus elbasvir was highly effective with a low rate of adverse events in this advanced chronic kidney disease difficult-to-treat population with an HCV genotype 1 or 4 infection.

摘要

患有慢性肾脏病晚期并接受直接作用抗病毒药物治疗的患者需要特别考虑合并症。在这里,我们在一项非随机、多中心、全国性观察性研究中评估了格拉替雷韦加艾尔巴韦尔在 93 例感染 HCV 基因型 1 或 4 且患有慢性肾脏病晚期的患者中的疗效和安全性。20 例 HCV 基因型 1a 患者、51 例 1b 患者、4 例未分类基因型 1 患者、17 例基因型 4 患者和 1 例基因型 6 患者每日接受一次格拉替雷韦加艾尔巴韦尔(100/50mg)治疗。所有患者均患有严重慢性肾脏病,其中 70 例为 G5 期,包括接受血液透析的患者(74.2%),23 例为 G4 期慢性肾脏病。33 例患者存在严重肝脏疾病(Metavir F3/F4)。90 例患者中有 87 例在治疗结束后 12 周达到持续病毒学应答。2 例患者发生病毒学突破,1 例患者在停药后复发。大多数患者接受了许多与合并症相关的合并用药(平均 7.7 种)。6 例患者发生严重不良事件,包括 3 例死亡,均与格拉替雷韦加艾尔巴韦尔治疗无关。因此,在 HCV 基因型 1 或 4 感染且患有慢性肾脏病晚期的难治性患者中,每日一次格拉替雷韦加艾尔巴韦尔治疗具有高疗效和低不良反应发生率。

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