实用肝脏病杂志 ›› 2018, Vol. 21 ›› Issue (5): 729-732.doi: 10.3969/j.issn.1672-5069.2018.05.019

• 病毒性肝炎 • 上一篇    下一篇

大剂量普通α-干扰素与聚乙二醇化α-干扰素联合利巴韦林治疗慢性丙型肝炎患者临床疗效及安全性比较研究*

曹风华, 经继生, 赵伟, 江英骙, 马洁   

  1. 212000 江苏省镇江市第二人民医院(曹风华); 江苏大学附属句容市人民医院感染病科(经继生); 东南大学附属第二医院(赵伟); 复旦大学附属华山医院感染病科(江英骙); 江苏大学(马洁)
  • 收稿日期:2018-01-24 出版日期:2018-09-10 发布日期:2018-09-27
  • 通讯作者: 经继生,E-mail: jrjjs2008@sina.com
  • 基金资助:
    江苏省卫计委科技支撑计划项目(编号:YG201508); 江苏大学科技支撑计划项目(编号:JLY20140076)

Clinical efficacy and safety of large dose of domestic interferon-α2b and ribavirin in the treatment of patients with chronic hepatitis C

Cao Fenghua, Jing Jisheng, Zhao Wei, et al.   

  1. Department of Infectious Diseases,Second People’s Hospital,Zhenjiang 212000,Jiangsu Province,China
  • Received:2018-01-24 Online:2018-09-10 Published:2018-09-27

摘要: 目的 通过与聚乙二醇化α-干扰素联合利巴韦林治疗疗效的比较,评价应用大剂量普通干扰素α2b联合利巴韦林治疗慢性丙型肝炎(CHC)患者的疗效及其安全性。方法 本文采用回顾性研究方法,对2012年1月~2016年1月收治的178例CHC患者接受普通α-干扰素联合利巴韦林(n=148)或聚乙二醇化干扰素联合利巴韦林(n=30)治疗48 w的效果进行分析,使用贝克曼公司生产的全自动生化分析仪检测血生化指标,采用定量RT-PCR法检测血清HCV RNA,采用ELISA法检测血清抗-HCV。病毒学应答定义为血清HCV RNA水平低于检测下限。结果 治疗前,普通干扰素治疗组血清ALT水平为(80.9±22.6) U/L,AST水平为(74.3±18.2) U/L,HCV RNA水平为(2.9±0.5)×105 copies/ml,与长效干扰素治疗组【(82.32±20.5) U/L、 (72.9±16.7) U/L和(2.8±0.5)×105 copies/ml】比,差异无统计学意义(P>0.05);在治疗4 w、12 w、24 w和48 w及随访至72 w时,普通干扰素治疗患者血清ALT复常率分别为79.7%、87.2%、90.5%、92.6%和86.5%,与长效干扰素治疗患者的76.7%、83.3%、90.0%、93.3%和90.0%比,无显著性统计学差异(P>0.05);血清HCV RNA阴转率分别为66.2%、71.0%、84.5%、90.5%和69.5%,与长效干扰素治疗患者的66.7%、73.3%、80.0%、90.0%和70.0%比,也无显著性统计学差异(P>0.05);长效干扰素治疗患者外周血WBC和PLT减少、脱发和食欲下降等不良反应发生率显著高于普通干扰素治疗组(P<0.05)。结论 应用大剂量普通干扰素α2b联合利巴韦林治疗CHC患者能获得与应用聚乙二醇化干扰素治疗方案类似的疗效,且副作用显著少于后者,但停药后长期疗效方面还需要进一步观察。

关键词: 慢性丙型肝炎, 国产α-干扰素, 聚乙二醇干扰素-α, 治疗

Abstract: Objective To evaluate the clinical efficacy and safety of large dose of domestic interferon-α2b and ribavirin in the treatment of patients with chronic hepatitis C(CHC). Methods In this study,we recruited 178 patients with CHC between January 2012 and January 2016,and 148 patients were treated with domestic interferon-α2b at dose of 6 MU qod in combination with ribavirin,and 30 patients were treated with pegylated interferon-α in combination with ribavirin. The regimen lasted for 48 weeks and all patients were followed-up for 24 weeks. Results At presentation,serum ALT level was (80.9±22.6)U/L,serum AST level was (74.3±18.2)U/L,and serum HCV RNA load was (2.9±0.5)×105copies/mL in patients receiving domestic interferon-α,no significant differences as compared to 【(82.32± 20.5) U/L,(72.9±16.7)u/L and (2.8±0.5)×105copies/ml】 in patients receiving pegylated interferon-α(P>0.05);at the end of 4 w,12 w,24 w and 48 w treatment and at the end of 24 w followed-up,serum ALT normalization rats in domestic interferon-treated patients were 79.7%,87.2%,90.5%,92.6% and 86.5%,without significant differences as compared to 76.7%,83.3%,90.0%,93.3% and 90.0% in pegylated interferon-α-treated patients(P>0.05);serum HCV RNA loss were 66.2%,71.0%,84.5%,90.5%and 69.5%,without significant differences as compared to 66.7%,73.3%,80.0%,90.0% and 70.0% in pegylated interferon-α-treated patients(P>0.05);the hypocytosis,hair loss and anorexia were more common and severe in pegylated interferon-α-treated patients(P<0.05). Conclusion The application of large -dose interferon α2b in combination with ribavirin in the treatment of patients with CHC might get the same clinical efficacy of pegylated interferon-α treatment,with less side effects, which needs further investigation and long-term observation.

Key words: Hepatitis C, Domestic interferon-α2b, Pegylated interferon, Treatment