实用肝脏病杂志 ›› 2025, Vol. 28 ›› Issue (3): 346-349.doi: 10.3969/j.issn.1672-5069.2025.03.007

• 病毒性肝炎 • 上一篇    下一篇

聚乙二醇化干扰素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*

王浩, 王清园, 沈琼, 许宇文   

  1. 200000 上海市 上海中医药大学附属曙光医院西药房(王浩,沈琼,许宇文);肝病科(王清园)
  • 收稿日期:2024-03-06 发布日期:2025-05-14
  • 作者简介:王浩,男,42岁,大学,主管药师。E-mail:13801634745@163.com
  • 基金资助:
    *上海市卫生健康委员会青年科研基金资助项目(编号:20214Y0502)

Satisfactory response to pegylated interferon α-2a and albavir/granrivir combination therapy in patients with chronic hepatitis C

Wang Hao, Wang Qingyuan, Shen Qiong, et al   

  1. Department of Pharmacy, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 200000, China
  • Received:2024-03-06 Published:2025-05-14

摘要: 目的 探讨聚乙二醇化干扰素α-2a(pegIFN-α-2a)联合艾尔巴韦/格拉瑞韦治疗慢性丙型肝炎(CHC)患者的疗效。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pegIFN-α-2a联合利巴韦林治疗或pegIFN-α-2a联合艾尔巴韦/格拉瑞韦治疗,两组均治疗24 w,随访24 w。常规检测血清HCV RNA载量和实验室指标。结果 观察组快速病毒学应答、治疗结束时病毒学应答和随访24 w时持续病毒学应答率分别为70.3%、97.3%和94.6%,显著高于对照组(分别为37.8%、62.2%和54.1%,P<0.05);在治疗4 w、12 w和随访24 w时,观察组血清HCV RNA载量分别为(1.6±0.8)lg u/ml、(1.5±0.9)lg u/ml和(1.2±0.3)lg u/ml,均显著低于对照组【分别为(4.3±0.9)lg u/ml、(4.5±0.8)lg u/ml和(3.2±0.5)lg u/ml,P<0.05】;在治疗结束时,观察组外周血WBC、RBC、PLT计数和Hb水平分别为(5.1±1.0)×109/L、(4.9±0.6)×1012/L、(101.8±17.5)×109/L和(120.5±19.5)g/L,显著高于对照组【分别为(3.3±0.9)×109/L、(4.3±0.5)×1012/L、(85.8±17.3)×109/L和(100.3±16.3)g/L,P<0.05】,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】。结论 应用pegIFN-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: 丙型肝炎, 艾尔巴韦, 格拉瑞韦, 聚乙二醇化干扰素α-2a, 治疗

Abstract: Objective This study was conducted to investigate efficacy of pegylated interferon α-2a (peg-IFNα-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 we assigned them to receive peg-IFNα-2a and albavir/granrivir combination therapy (observation, n=37) for 12 weeks, or to receive peg-IFNα-2a and ribavirin combination therapy (control, n=37) for 24 weeks. Serum HCV RNA loads and other laboratory tests were recorded. Results Rapid virological response rate, end of treatment virological response rate and sustained virological response rate in observation group were 70.3%, 97.3% and 94.6%, all significantly higher than 37.8%, 62.2% and 54.1% in the control (P<0.05); by week 4, week 12 and week 24 of follow-up, serum HCV RNA loads in the observation were (1.6±0.8)lg u/ml, (1.5±0.9)lg u/ml and (1.2±0.3)lg u/ml, all significantly lower than [(4.3±0.9)lg u/ml, (4.5±0.8)lg u/ml and (3.2±0.5)lg u/ml, respectively, P<0.05] in the control; by end of antiviral treatment, peripheral blood WBC, RBC, PLT counts and Hb concentration in the observation were (5.1±1.0)×109/L, (4.9±0.6)×1012/L, (101.8±17.5)×109/L and (120.5±19.5)g/L, all significantly higher than [(3.3±0.9)×109/L, (4.3±0.5)×1012/L, (85.8±17.3)×109/L and (100.3±16.3)g/L, respectively, P<0.05] in the control, and serum ALT and AST levels 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 group. Conclusion Combination of peg-IFN α-2a and albavir/graniclovir in treatment of patients with CHC could obtain a satisfactory antiviral efficacy, improve liver function recovery.

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