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艾尔巴韦和格拉瑞韦用于近期有注射吸毒史人群的丙型肝炎病毒1型感染治疗(DARLO-C):一项开放标签、单臂、4期、多中心试验。

Elbasvir and grazoprevir for hepatitis C virus genotype 1 infection in people with recent injecting drug use (DARLO-C): An open-label, single-arm, phase 4, multicentre trial.

作者信息

Grebely Jason, Read Phillip, Cunningham Evan B, Weltman Martin, Matthews Gail V, Dunlop Adrian, Montebello Mark, Martinello Marianne, Gilliver Rosie, Marks Philippa, Applegate Tanya L, Dore Gregory J

机构信息

Viral Hepatitis Clinical Research Program The Kirby Institute, UNSW Sydney Sydney Australia.

Kirketon Road Centre Sydney Australia.

出版信息

Health Sci Rep. 2020 Mar 15;3(2):e151. doi: 10.1002/hsr2.151. eCollection 2020 Jun.

Abstract

BACKGROUND AND AIMS

Direct-acting antiviral therapy for hepatitis C virus (HCV) is effective, but few prospective studies among people with ongoing injecting drug use exist. This study evaluated the efficacy of elbasvir/grazoprevir in people with HCV genotype 1/4 (G1/4) infection and recent injecting drug use. An exploratory aim evaluated the feasibility of fingerstick point-of-care HCV RNA testing prior to and following treatment.

METHODS

DARLO-C (http://clinicaltrials.gov: NCT02940691) is an open-label phase 4 trial. Participants were recruited between May 2017 and March 2018 from two drug treatment clinics, two hospital clinics, and one community clinic in Australia. Inclusion criteria included recent injection drug use (previous 6 months) and HCV G1/4 infection. Exclusion criteria included prior HCV treatment and decompensated liver disease. Participants received elbasvir/grazoprevir once-daily for 12 weeks. The primary endpoint was undetectable HCV RNA 12 weeks post-treatment (SVR). Fingerstick whole-blood samples were tested using the Xpert HCV Viral Load Fingerstick (Xpert HCV VL Fingerstick) assay and compared to the Aptima HCV Quant Dx Assay on plasma samples.

RESULTS

Of a planned 150 participants, 32 were enrolled due to slower than anticipated recruitment [median age 46 years, 10 (31%) female, 29 (91%) G1a]. Eighteen (56%) were receiving opioid agonist therapy and 29 (91%) injected in the previous month. Twenty-six (81%) of 32 completed treatment (lost to follow-up, n = 5; incarceration, n = 1). There were no virological failures. Twenty-four (75%, 95% CI 59%-91%) of 32 achieved SVR. Two participants who completed treatment did not have SVR (loss to follow-up, n = 1; refused test, n = 1). Among paired samples (n = 36), sensitivity of the Xpert HCV VL Fingerstick assay for HCV RNA detection was 100.0% (95% CI 75.3%-100.0%) and specificity was 95.7% (95% CI 78.1%-99.9%).

CONCLUSION

Elbasvir/grazoprevir is effective among people with HCV G1 with recent injecting drug use. Implementation of point-of-care HCV RNA testing was feasible, but the high error rate requires investigation.

摘要

背景与目的

丙型肝炎病毒(HCV)的直接抗病毒治疗有效,但针对仍在注射吸毒人群的前瞻性研究较少。本研究评估了艾尔巴韦/格拉瑞韦在HCV 1/4型(G1/4)感染且近期有注射吸毒行为人群中的疗效。一项探索性目的是评估治疗前后即时检测指尖血HCV RNA检测的可行性。

方法

DARLO-C(http://clinicaltrials.gov:NCT02940691)是一项开放标签的4期试验。2017年5月至2018年3月期间,从澳大利亚的两家戒毒诊所、两家医院诊所和一家社区诊所招募参与者。纳入标准包括近期注射吸毒行为(过去6个月内)和HCV G1/4感染。排除标准包括既往HCV治疗史和失代偿性肝病。参与者接受艾尔巴韦/格拉瑞韦每日一次,共12周。主要终点是治疗后12周HCV RNA检测不到(SVR)。使用Xpert HCV病毒载量即时检测(Xpert HCV VL即时检测)法检测指尖全血样本,并与血浆样本上的Aptima HCV定量Dx检测法进行比较。

结果

计划招募150名参与者,由于招募速度慢于预期,仅32名入组[中位年龄46岁,10名(31%)女性,29名(91%)G1a型]。18名(56%)正在接受阿片类激动剂治疗,29名(91%)在上个月有注射行为。32名参与者中有26名(81%)完成治疗(失访5名;监禁1名)。无病毒学失败病例。32名参与者中有24名(75%,95%CI 59%-91%)实现SVR。两名完成治疗的参与者未实现SVR(失访1名;拒绝检测1名)。在配对样本(n = 36)中,Xpert HCV VL即时检测法检测HCV RNA的敏感性为100.0%(95%CI 75.3%-100.0%),特异性为95.7%(95%CI 78.1%-99.9%)。

结论

艾尔巴韦/格拉瑞韦在近期有注射吸毒行为的HCV G1型人群中有效。即时检测HCV RNA检测的实施是可行的,但高错误率需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d129/7136479/11516e7fe70a/HSR2-3-e151-g001.jpg

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