实用肝脏病杂志 ›› 2025, Vol. 28 ›› Issue (5): 683-686.doi: 10.3969/j.issn.1672-5069.2025.05.011

• 病毒性肝炎 • 上一篇    下一篇

达卡他韦联合阿舒瑞韦治疗基因1b型慢性丙型肝炎患者疗效研究*

辛文渊, 李玉薇, 吴君   

  1. 250100 济南市 山东大学药学院(辛文渊);附属齐鲁医院消化内科(李玉薇,吴君)
  • 收稿日期:2024-11-19 出版日期:2025-09-10 发布日期:2025-09-19
  • 通讯作者: 吴君,E-mail:wujunbw2013@163.com
  • 作者简介:辛文渊,女,20岁,大学本科。E-mail:xinwyqd@163.com
  • 基金资助:
    *山东省自然科学基金青年基金资助项目(编号:ZR2022QH104)

Efficacy of dalatavir combination with asulivir in the treatment of patients with chronic hepatitis C with genotype 1b infection

Xin Wenyuan, Li Yuwei, Wu Jun   

  1. School of Pharmaceutical Sciences, Shandong University, Jinan 250100, Shandong Province, China
  • Received:2024-11-19 Online:2025-09-10 Published:2025-09-19

摘要: 目的 探讨应用达拉他韦(DCV)和阿舒瑞韦(ASV)联合治疗基因 1b型慢性丙型肝炎(CHC)患者的疗效。方法 2020年1月~2023年1月我院诊治的56例基因1b型CHC患者,其中1例在治疗期间退出,其他55例均接受并完成12 w的DCV联合ASV治疗,治疗结束后随访24 w。使用美国罗氏公司提供的COBAS Taqman HCV实时定量PCR检测平台检测血清HCV RNA。结果 55例CHC患者基线血清HCV RNA载量为(6.0±0.6)lg IU/mL,在抗病毒治疗4 w、12 w和随访24 w时,分别为(4.3±0.5)lg IU/mL、(<1.7)lg IU/mL和(<1.7)lg IU/mL,病毒学应答率(VR)分别为20.0%、100.0%和100.0%;55例CHC患者基线血清AST、ALT和天冬氨酸氨基转移酶/血小板计数比值分别为(74.5±24.5)U/L、(83.0±9.6)U/L和(4.3±1.7),在治疗结束和随访24 w末均恢复正常;55例基因1b型CHC患者在治疗结束随访24 w时,外周血白细胞计数、中性粒细胞计数和PLT计数均显著上升(P<0.05),而血红蛋白水平无显著变化(P>0.05)。结论 应用DCV和ASV联合治疗HCV 1b型感染的CHC患者近期疗效好,安全性高,其远期疗效还有待于进一步观察。

关键词: 丙型肝炎, 丙型肝炎病毒基因1b型, 达拉他韦, 阿舒瑞韦, 治疗

Abstract: Objective The aim of this study was to investigate efficacy of dacatevir (DCV) and asurevir (ASV) combination in the treatment of patients with chronic hepatitis C (CHC) with hepatitis C virus (HCV) genotype 1b infection. Methods 56 patients with CHC with HCV genotype 1b infection were recruited in our hospital between January 2020 and January 2023, and 55 patients but 1 patient dropped out received dacatavir plus asulivir combination treatment for 12 weeks, and all were followed-up for 24 weeks. Serum HCV RNA loads were determined by RT-PCR, and aspartate aminotransferase/platelet ratio (APRI) was routinely calculated. Results At baseline, serum HCV RNA load in the 55 patients with CHC was (6.0±0.6)lg IU/mL, and it transferred to (4.3±0.5)lg IU/mL, (<1.7)lg IU/mL and (<1.7)lg IU/mL 4 weeks and 12 weeks during antiviral therapy and 24 weeks of follow-up, with complete virological response(CVR) of 20.0%, 100.0% and 100.0%, respectively; serum AST, ALT levels and APRI were (74.5±24.5)U/L, (83.0±9.6)U/L and (4.3±1.7), and all returned to normal at end of antiviral regimen and at end of 24 week of follow-up; peripheral white blood cell count, neutrophils count and platelet count elevated to normal(P<0.05), and blood hemoglobin level didn’t change (P>0.05)at end of 24 week of follow-up. Conclusion Combination of DCV and ASV antiviral therapy have a good short-term efficacy in the treatment of patients with CHC with hepatitis C virus genotype 1b infection, and long-term efficacy needs further observation.

Key words: Hepatitis C, Hepatitis C viral genotype 1b, Dalatavir, Asurivir, Therapy