实用肝脏病杂志 ›› 2021, Vol. 24 ›› Issue (1): 35-38.doi: 10.3969/j.issn.1672-5069.2021.01.010

• 病毒性肝炎 • 上一篇    下一篇

达诺瑞韦联合长效α-干扰素治疗基因3型慢性丙型肝炎患者疗效研究

杨晓冬, 贾婷, 张秀灵, 高斯媛, 余向琼, 李冬玲, 喻明丽, 林潮双   

  1. 650041 昆明市第三人民医院肝病二科(杨晓冬,贾婷,张秀灵,高斯媛,余向琼,李冬玲);
    药学部(喻明丽);
    广州中山大学附属第三医院感染病科(林潮双)
  • 出版日期:2021-01-10 发布日期:2021-01-19
  • 通讯作者: 杨晓冬,女,45岁,大学本科,副主任医师
       通讯作者:喻明丽,E-mail:717568354@qq.com
  • 作者简介:杨晓冬,女,45岁,大学本科,副主任医师

Short-term efficacy of danorevir and peginterferon-α in the treatment of patients with genotype 3 infected chronic hepatitis C

Yang Xiaodong,Jia Ting,Zhang Xiuling, et al   

  1. Second Department of Liver Diseases, Third People's Hospital, Kunming 650041,Yunnan Province, China
  • Online:2021-01-10 Published:2021-01-19

摘要: 目的 研究在达诺瑞韦基础上联合长效α-干扰素治疗基因3型慢性丙型肝炎(CHC)患者的临床疗效。方法 2017年10月~2019年5月我院收治的132例基因3型CHC患者,其中66例(对照组)接受聚乙二醇干扰素α-2a联合利巴韦林治疗24周,另66例(观察组)接受聚乙二醇干扰素α-2a和利巴韦林治疗的基础上,加用利托那韦和达诺瑞韦联合治疗12周。所有患者随访24周。结果 在治疗2 w、4 w和12 w末,观察组病毒学应答率分别为90.9%、97.0%和100.0%,显著高于对照组的66.7%、75.8%和81.8%(P<0.05);在治疗结束后24 w随访时,观察组持续病毒学应答率(SVR)为92.4%,显著高于对照组的74.2%(P<0.05);在治疗12 w末,两组外周血白细胞计数、血小板计数和血红蛋白水平变化无统计学差异(P>0.05),两组不良反应发生率比较差异也无统计学意义(P>0.05)。结论 应用利托那韦和达诺瑞韦联合标准治疗方案治疗基因3型CHC患者临床疗效确切,安全性较好,值得进一步观察。

关键词: 慢性丙型肝炎, 达诺瑞韦, 利托那韦, 聚乙二醇干扰素α-2a, 利巴韦林, 治疗

Abstract: Objective The aim of this study was to investigate the short-term efficacy of danorevir and peginterferon-α in the treatment of patients with genotype 3 infected chronic hepatitis C (CHC). Methods 132 patients with genotype 3 infected CHC were admitted to our hospital between October 2017 and May 2019, and 66 patients were treated with peginterferon-2a and ribavirin for 24 weeks, and another 66 patients were treated with ritonavir and danorevir at base of standardized therapy for 12 weeks. All patients were followed-up for 24 weeks. Results At the end of 2 week, 4 week and 12 week treatment, the virological response rates in the combination group were 90.9%, 97.0% and 100.0%, respectively, significantly higher than 66.7%, 75.8% and 81.8% in standardized therapy-treated group (P<0.05); at the end of 24 week of follow-up after treatment, the sustained virological response (SVR) in the combination group was 92.4%, significantly higher than 74.2% in the control group (P<0.05); there were no statistically significant differences in white blood cell counts, platelet counts and hemoglobin levels in the two groups (P>0.05) and there wereno significant differences in the incidences of adverse reactions between the two groups (P>0.05).Conclusion The application of ritonavir and danorevir at base of standardized therapy in the treatment of patients with CHC and genotype 3 infection is efficacious and safe, which warrants further investigation.

Key words: Hepatitis C, Danorevir, Ritonavir, Pegylated interferon α-2a, Ribavirin, Therapy