首页> 外文期刊>World Journal of Gastroenterology >Different doses of consensus interferon plus ribavirin in patients with hepatitis C virus genotype 1 relapsed after interferon monotherapy: a randomized controlled trial.
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Different doses of consensus interferon plus ribavirin in patients with hepatitis C virus genotype 1 relapsed after interferon monotherapy: a randomized controlled trial.

机译:干扰素单药治疗后,丙型肝炎病毒基因型1的患者不同剂量的共识性干扰素加病毒唑联合用药复发:一项随机对照试验。

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AIM: To assess the efficacy of different schedules of consensus interferon (CIFN) plus ribavirin in retreating chronic hepatitis C patients who relapsed after recombinant interferon (rIFN) monotherapy. METHODS: Forty-five patients (34 males and 11 females) with chronic hepatitis due to hepatitis C virus (HCV) genotype 1 who relapsed after a previous course of rIFN monotherapy were randomized to receive 9 mug CIFN three times per week for 52 wk (group A, n = 22) or 18 mug CIFN three times per week for 52 wk (group B, n = 23) in combination with ribavirin 800 to 1200 mg daily for 52 wk (according to body weight). Virological response was evaluated at week 24 (EVR), at the end of treatment (ETR) and at 76 wk (SVR). RESULTS: By intention-to-treat analysis, subjects in group A had an EVR in 35% of cases, an ETR in 35% and a SVR in 27.3% of cases. Subjects in group B had an EVR in 32% of cases, an ETR in 35% and a SVR in 26.1% of cases. Treatment was stopped because of adverse effects (mostly intolerance) in15 patients (6 in group A and 9 in group B). IFN dose reduction was needed in 2 patients (1 in group A and 1 in group B). Ribavirin dose was reduced in 2 patients in group A and 1 in group B respectively. Among the 15 subjects who received at least 80% of the intended schedule, the rate of SVR was 80% (6 in group A and 6 in group B). CONCLUSION: CIFN in combination with ribavirin when given to HCV genotype 1 relapsers after rIFN monotherapy obtains an unsatisfactory rate of sustained viral clearance independently of dosage of the drug. This may be due to its scarce tolerability.
机译:目的:评估共识性干扰素(rIFN)单药治疗后复发的慢性丙型肝炎患者的治疗方案。方法:45例因丙型肝炎病毒(HCV)基因1型慢性丙型肝炎的患者(在先前的rIFN单药疗程后复发)被随机分配,每周接受三次9杯CIFN,每周52周( A组,n = 22)或18杯CIFN,每周52次(52周)(B组,n = 23),结合利巴韦林每天800至1200 mg,52周(根据体重)。在治疗第24周(EVR),治疗结束(ETR)和第76周(SVR)评估病毒学应答。结果:通过意向治疗分析,A组受试者的EVR为35%,ETR为35%,SVR为27.3%。 B组受试者的EVR占32%,ETR占35%,SVR占26.1%。 15位患者(A组6位,B组9位)由于不良反应(大多为不耐受)而停止治疗。 2名患者(A组1例,B组1例)需要降低IFN剂量。利巴韦林剂量分别在A组2例和B组1例中降低。在接受了至少80%的预定时间表的15名受试者中,SVR的发生率为80%(A组为6名,B组为6名)。结论:rIFN单药治疗后,将CIFN与利巴韦林联合用于HCV基因型1复发者,获得的持续病毒清除率不令人满意,与药物剂量无关。这可能是由于其缺乏耐受性。

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