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延长疗程使用500万单位干扰素联合利巴韦林治疗慢性丙型肝炎复发患者的疗效

Efficacy of prolonged 5 million units of interferon in combination with ribavirin for relapser patients with chronic hepatitis C.

作者信息

Fattovich G, Zagni I, Fornaciari G, Minola E, Fabris P, Boccia S, Giusti M, Abbati G, Felder M, Rovere P, Redaelli A, Tonon A, Montanari R, Paternoster C, Distasi M, Castagnetti E, Tositti G, Rizzo C, Suppressa S, Pantalena M, Lomonaco L, Scattolini C, Tagger A

机构信息

Servizio Autonomo Clinicizzato di Gastroenterologia, Università di Verona, Verona, Italy.

出版信息

J Viral Hepat. 2003 Mar;10(2):111-7. doi: 10.1046/j.1365-2893.2003.00409.x.

Abstract

summary. Retreatment of relapser patients with chronic hepatitis C with the standard dose of interferon (IFN) of 3 million units (MU) thrice weekly (tiw) plus ribavirin for 24 weeks achieves a sustained response in 30 and 73% of patients with genotype 1 and 2 or 3, respectively. The aim of this study was to evaluate the efficacy and safety of IFN alpha-2b induction therapy, followed by prolonged treatment with a high dose of IFN alpha-2b plus ribavirin in relapser patients. A total of 119 patients were randomized to receive IFN alpha-2b 5 MU daily (Group A: 59 patients) or IFN alpha-2b 5 MU tiw (Group B: 60 patients) for 4 weeks followed by IFN (5 MU tiw) and ribavirin (1000-1200 mg/day) for 48 weeks in both groups. The primary end point was hepatitis C virus (HCV)-RNA clearance at week 24 after the end of treatment. A sustained virological response (SVR) was achieved in 68 and 60% of Group A and B patients, respectively (P = 0.37). Logistic regression analysis identified genotype 2 or 3 as the only independent factor associated with response, whereas induction regimen and baseline viraemia levels did not affect the response. The overall SVR was 53 and 72% in patients with genotype 1 or 4 and 2 or 3, respectively. In conclusion, induction IFN therapy does not enhance the SVR to a 48-week combination therapy. Our study suggests that relapsed patients with genotype 1 or 4 may achieve significant response rates of approximately 50%, if retreated with 5 MU tiw IFN plus ribavirin for 48 weeks.

摘要

摘要。慢性丙型肝炎复发患者采用标准剂量300万单位(MU)的干扰素(IFN)每周三次(tiw)加利巴韦林进行24周再治疗,1型和2或3型患者分别有30%和73%获得持续应答。本研究的目的是评估IFNα-2b诱导治疗,随后对复发患者采用高剂量IFNα-2b加利巴韦林延长治疗的疗效和安全性。总共119例患者被随机分为两组,A组59例患者接受每日5 MU的IFNα-2b治疗,B组60例患者接受每周三次5 MU的IFNα-2b治疗,为期4周,之后两组均接受每周三次5 MU的IFN和1000 - 1200 mg/天的利巴韦林治疗48周。主要终点是治疗结束后第24周丙型肝炎病毒(HCV)-RNA清除情况。A组和B组患者分别有68%和60%获得持续病毒学应答(SVR)(P = 0.37)。逻辑回归分析确定2或3型基因型是唯一与应答相关的独立因素,而诱导方案和基线病毒血症水平不影响应答。1或4型和2或3型患者的总体SVR分别为53%和72%。总之,诱导IFN治疗不会提高48周联合治疗的SVR。我们的研究表明,1或4型复发患者如果采用每周三次5 MU的IFN加利巴韦林再治疗48周,可能获得约50%的显著应答率。

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