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一项关于艾尔巴韦-格拉瑞韦联合治疗法国慢性丙型肝炎的应用与疗效的观察性、前瞻性、多中心研究(ZEPHYR研究)。

An observational, prospective, multicenter study on the utilization and effectiveness of elbasvir-grazoprevir treatment association for chronic hepatitis C in France (ZEPHYR study).

作者信息

Bronowicki Jean-Pierre, Miailhes Patrick, Hanslik Bertrand, Ouzan Denis, Larrey Dominique, Riachi Ghassan, Truchi Régine, Jouannaud Vincent, Pospait Dan, Abergel Armand, Causse Xavier, Perot Stéphanie, Skrzypski Jérémy, De Hautecloque Astrid, Spampinato Axelle, Mariot Philippe, Sogni Philippe

机构信息

Hépato-gastroentérologie, CHRU Nancy, INSERM 1256, Université de Lorraine, Nancy, CHRU Vandoeuvre les Nancy Nancy France.

Infectious disease Unit, Hôpital Croix Rousse, HCL Lyon France.

出版信息

Health Sci Rep. 2022 Dec 5;6(1):e619. doi: 10.1002/hsr2.619. eCollection 2023 Jan.

Abstract

BACKGROUND AND AIM

The efficacy and safety profiles of elbasvir-grazoprevir (EBR/GZR) has been established in more than 10 clinical trials. However, the characteristics of patients treated in routine clinical practice may differ. The present study was therefore designed to assess the real-life effectiveness of EBR/GZR therapy in the general population and among subgroups with a high hepatitis C virus (HCV) prevalence in France.

METHODS

The Zephyr study was designed as a French, multicentre, prospective, observational study on EBR/GZR use and effectiveness in current practice in chronic hepatitis C patients. These results are based on data regarding the adult patients who received at least one dose of EBR/GZR between December 2017 and June 2019 in 67 French hospitals and clinics.

RESULTS

Overall, 478 patients were included. The Full Analysis Set corresponded to the 467 patients who met all the inclusion criteria and none of the exclusion criteria. Gender was balanced and the mean age was 55.7 ± 13.3 years. The patients were mainly treatment-naive (89.5%) and infected with Genotype 1b (70.4%). Among the 75 patients with HCV Gt1a genotype, 56% had HCV RNA ≥ 800,000 IU/ml. F3-F4 fibrosis stage involved 24.2% of our population. Our subgroups were distributed among 110 migrants (23.6%), 58 (15.3%) using opioid agonist treatment, including people who inject drugs, 30 (6.8%) with chronic kidney disease Stages 3-5, 9 (1.9%) with an inherited blood disorder, and 4 (0.9%) coinfected with HIV. The remaining 269 (58.7%) were included in the general population subgroup. Overall, sustained virologic response 12 weeks after the end of treatment reached 98.0% and remained consistent among genotype, HCV RNA values, fibrosis stage, and the subgroup of interest. The rate of Alcohol Use Disorders Identification Test-Consumption​​​ and Life Habit questionnaire completion was high at each visit, with data suggesting alcohol consumption decrease and an improvement in quality of life.

CONCLUSIONS

Using real-world evidence data on a French population representative of HCV patients, we confirmed the results obtained during EBR/GZR development program.

摘要

背景与目的

艾尔巴韦-格拉瑞韦(EBR/GZR)的疗效和安全性已在10多项临床试验中得到证实。然而,常规临床实践中接受治疗的患者特征可能有所不同。因此,本研究旨在评估EBR/GZR疗法在法国普通人群以及丙型肝炎病毒(HCV)高流行亚组中的实际疗效。

方法

Zephyr研究设计为一项关于EBR/GZR在慢性丙型肝炎患者当前治疗实践中的使用情况和疗效的法国多中心前瞻性观察性研究。这些结果基于2017年12月至2019年6月期间在法国67家医院和诊所接受至少一剂EBR/GZR治疗的成年患者的数据。

结果

总共纳入了478例患者。完整分析集包括467例符合所有纳入标准且无排除标准的患者。性别均衡,平均年龄为55.7±13.3岁。患者主要为初治患者(89.5%),感染基因型1b(70.4%)。在75例HCV Gt1a基因型患者中,56%的患者HCV RNA≥800,000 IU/ml。F3-F4纤维化阶段的患者占总体的24.2%。我们的亚组包括110名移民(23.6%)、58名(15.3%)使用阿片类激动剂治疗的患者(包括注射吸毒者)、30名(6.8%)患有3-5期慢性肾脏病的患者、9名(1.9%)患有遗传性血液疾病的患者以及4名(0.9%)合并感染HIV的患者。其余269名(58.7%)被纳入普通人群亚组。总体而言,治疗结束后12周的持续病毒学应答率达到98.0%,在基因型、HCV RNA值、纤维化阶段以及感兴趣的亚组中保持一致。每次随访时酒精使用障碍识别测试-消费量和生活习惯问卷的完成率都很高,数据表明饮酒量减少且生活质量有所改善。

结论

利用代表HCV患者的法国人群的真实世界证据数据,我们证实了EBR/GZR研发项目期间获得的结果。

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