实用肝脏病杂志 ›› 2025, Vol. 28 ›› Issue (1): 40-43.doi: 10.3969/j.issn.1672-5069.2025.01.011

• 病毒性肝炎 • 上一篇    下一篇

聚乙二醇干扰素α-2a联合艾尔巴韦/格拉瑞韦治疗慢性丙型肝炎患者疗效研究*

王菲, 刘迎宾, 赵媛媛   

  1. 710032 西安市 空军军医大学第一附属医院西京医院药剂科(王菲, 刘迎宾);西安存济医学中心药剂科(赵媛媛)
  • 收稿日期:2023-09-28 出版日期:2025-01-10 发布日期:2025-02-07
  • 通讯作者: 刘迎宾,E-mail:yingbin0216@163.com
  • 作者简介:王菲,女,37岁,大学本科,主管药师。E-mail:ym876543212018@163.com
  • 基金资助:
    *陕西省自然科学基础研究计划重点项目(编号:2021JZ-29)

Antiviral efficacy of pegylated interferon α-2a and albavir/granrivir combination in the treatment of patients with chronic hepatitis C

Wang Fei, Liu Yingbin, Zhao Yuanyuan   

  1. Department of Pharmacy, Xijing Hospital, First Affiliated Hospital, Air Force Military Medical University, Xi'an 710032, Shaanxi Province, China
  • Received:2023-09-28 Online:2025-01-10 Published:2025-02-07

摘要: 目的 探讨应用聚乙二醇干扰素α-2a联合艾尔巴韦/格拉瑞韦治疗慢性丙型肝炎(CHC)患者的效果。方法 2018年1月~2022年1月我院诊治的CHC患者74例,被随机分为对照组37例和观察组37例,分别给予聚乙二醇干扰素α-2a联合利巴韦林治疗24周或聚乙二醇干扰素α-2a联合艾尔巴韦/格拉瑞韦治疗12周。在治疗结束后,随访24周。结果 观察组快速病毒学应答率、早期病毒学应答率、治疗结束病毒学应答率和持续病毒学应答率分别为70.3%、89.2%、89.2%和94.6%,均显著高于对照组的37.8%、54.1%、62.2%和54.1%(P<0.05);治疗4周、12周、24周和随访24 周时,观察组血清HCV RAN载量分别为(1.6±0.8)lg copies/L、(1.2±0.4)lg copies/L、(1.2±0.4)lg copies/L和(1.2±0.3)lg copies/L,显著低于对照组[分别为(4.3±0.9) lg copies/L、(4.5±0.8)lg copies/L、(3.2±0.5)lg copies/L和(3.2±0.5)lg copies/L, P<0.05];在治疗结束时,观察组血清ALT和AST水平分别为(34.6±5.8)U/L和(36.4±6.9)U/L,均显著低于对照组[分别为(46.3±6.9)U/L和(49.1±7.5)U/L,P<0.05],而两组血细胞均降低(P>0.05)。结论 应用聚乙二醇干扰素α-2a联合艾尔巴韦/格拉瑞韦治疗CHC患者病毒学应答率高,有利于肝功能恢复,显示出良好的治疗前景。

关键词: 慢性丙型肝炎, 聚乙二醇干扰素α-2a, 艾尔巴韦, 格拉瑞韦, 治疗

Abstract: Objective The purpose of this study was to investigate the antiviral efficacy of pegylated interferon α-2a and albavir/granrivir combination in the treatment of patients with chronic hepatitis C (CHC). Methods 74 patients with CHC were encountered in our hospital between January 2018 and January 2022, and were randomly divided into control (n=37) and observation (n=37) group, receiving pegylated interferon α-2a and ribavirin therapy for 24 weeks, or pegylated interferon α-2a and albavir/granrivir combination therapy for 12 weeks. All patients were followed-up for 24 weeks after discontinuation of the antiviral treatment. Results The rapid virological response, early virological response, end of treatment virological response and sustained virological response in the observation were 70.3%, 89.2%, 89.2% and 94.6%, all significantly higher than 37.8%, 54.1%, 62.2% and 54.1%(P<0.05) in the control; at treatment week 4, week 12, week 24 and at follow-up 24 week, serum HCV RAN loads in the observation were (1.6±0.8)lg copies/L, (1.2±0.4)lg copies/L, (1.2±0.4)lg copies/L and (1.2±0.3)lg copies/L, all significantly lower than [(4.3±0.9) lg copies/L, (4.5±0.8)lg copies/L, (3.2±0.5)lg copies/L and (3.2±0.5)lg copies/L, respectively, P<0.05] in the control group; at the end of antiviral treatment, serum ALT and AST levels in the observation were (34.6±5.8)U/L and 36.4±6.9)U/L, both much lower than [(46.3±6.9)U/L and (49.1±7.5)U/L, respectively, P<0.05] in the control, while white blood cell counts, platelet counts and hemoglobin concentration in the two groups decreased obviously, without significant differences (P>0.05). Conclusion The combination of pegylated interferon α-2a and albavir/graniclovir therapy in the treatment of patients with CHC has a high virological response rate, which is beneficial to the recovery of liver function tests, showing a promising therapeutic outcomes.

Key words: Hepatitis C, Pegylated interferon α-2a, Albavir, Granrivir, Therapy