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对复发或对单独使用干扰素无反应的慢性丙型肝炎患者,分别用干扰素-α2b加利巴韦林进行24周与48周的再治疗。

Retreatment for 24 vs 48 weeks with interferon-alpha2b plus ribavirin of chronic hepatitis C patients who relapsed or did not respond to interferon alone.

作者信息

Enríquez J, Gallego A, Torras X, Pérez-Olmeda T, Diago M, Soriano V, Luján M S, García-Samaniego J

机构信息

Department of Gastroenterology, Hospital de la Sta Creu i St Pau, Barcelona, Spain.

出版信息

J Viral Hepat. 2000 Nov;7(6):403-8. doi: 10.1046/j.1365-2893.2000.00243.x.

DOI:10.1046/j.1365-2893.2000.00243.x
PMID:11115050
Abstract

We assessed the efficacy of interferon (IFN) plus ribavirin over 24 or 48 weeks for the retreatment of patients with chronic hepatitis C who had relapsed or did not respond to a previous course of IFN. One-hundred and twenty patients (69 non-responders and 51 relapsers) were randomly assigned to receive IFN-alpha2b (3 million units thrice weekly) plus ribavirin (1,000-1,200 mg per day) for 24 weeks (group A: 58 patients) or 48 weeks (group B: 62 patients). Treatment was discontinued at week 12 if the alanine aminotransferase (ALT) level remained elevated. The rate of sustained response was 15.5% in group A and 37.1% in group B (P = 0.013). Relapsers treated for 48 weeks had a sustained response rate of 66.6% compared with a sustained response rate of only 25% in those treated for 24 weeks (P = 0.004). Moreover, a sustained response was seen in 14.3% of non-responders treated for 48 weeks and in 8.8% of those treated for 24 weeks (P = 0.71). Fifty-three per cent of patients with a normal ALT level and undetectable hepatitis C virus (HCV) RNA at week 12 had a sustained response compared with 14% of those who were HCV RNA positive at week 12 (P < 0.001). Independent predictive factors of sustained response were: therapy for 48 weeks (P = 0.0026), relapse after IFN treatment (P = 0.0006), loss of HCV RNA at week 12 (P = 0.0008) and HCV genotype non-1 (P = 0.024). Hence, in patients with chronic hepatitis C who failed to respond to a previous course of IFN monotherapy, combination therapy with IFN plus ribavirin for 48 weeks seems to be more effective than IFN plus ribavirin for 24 weeks.

摘要

我们评估了干扰素(IFN)联合利巴韦林治疗24周或48周对既往使用IFN治疗复发或无反应的慢性丙型肝炎患者再次治疗的疗效。120例患者(69例无反应者和51例复发者)被随机分配接受α-2b干扰素(300万单位,每周3次)联合利巴韦林(每日1000 - 1200mg)治疗24周(A组:58例患者)或48周(B组:62例患者)。如果丙氨酸氨基转移酶(ALT)水平持续升高,则在第12周停止治疗。A组的持续应答率为15.5%,B组为37.1%(P = 0.013)。接受48周治疗的复发者持续应答率为66.6%,而接受24周治疗者的持续应答率仅为25%(P = 0.004)。此外,接受48周治疗的无反应者中14.3%出现持续应答,接受24周治疗者中这一比例为8.8%(P = 0.71)。第12周ALT水平正常且丙型肝炎病毒(HCV)RNA检测不到的患者中53%出现持续应答,而第12周HCV RNA阳性的患者中这一比例为14%(P < 0.001)。持续应答的独立预测因素为:治疗48周(P = 0.0026)、IFN治疗后复发(P = 0.0006)、第12周HCV RNA转阴(P = 0.0008)和HCV非1型基因型(P = 0.024)。因此,对于既往IFN单药治疗无效的慢性丙型肝炎患者,IFN联合利巴韦林治疗48周似乎比治疗24周更有效。

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引用本文的文献

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Cochrane Database Syst Rev. 2013 Jan 31;2013(1):CD003617. doi: 10.1002/14651858.CD003617.pub2.
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A randomized trial of induction doses of interferon alone or in combination with ribavirin or ribavirin plus amantadine for treatment of nonresponder patients with chronic hepatitis C.一项关于单独使用诱导剂量干扰素或联合利巴韦林或利巴韦林加金刚烷胺治疗慢性丙型肝炎无反应患者的随机试验。
J Gastroenterol. 2007 May;42(5):362-7. doi: 10.1007/s00535-007-2006-3. Epub 2007 May 25.
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Treatment of chronic HCV infection in special populations.
特殊人群中慢性丙型肝炎病毒感染的治疗
Int J Med Sci. 2006;3(2):69-74. doi: 10.7150/ijms.3.69. Epub 2006 Apr 1.