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Randomised double blind placebo controlled trial of interferon ribavirin and amantadine versus interferon ribavirin and placebo in treatment naïve patients with chronic hepatitis C

机译:干扰素利巴韦林和金刚烷胺与干扰素利巴韦林和安慰剂的随机双盲安慰剂对照试验治疗初治的慢性丙型肝炎患者

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摘要

>Background and aim: In this study, we compared the efficacy of triple therapy (interferon alfa, ribavirin, and amantadine) with standard therapy (interferon alfa and ribavirin) in treatment naïve patients with chronic hepatitis C virus (HCV).>Methods: In this prospective, randomised, double blind, placebo controlled, multicentre study, 85 patients (amantadine group) received a three drug regimen of interferon alfa-2b 3 million units three times per week, ribavirin 1000–1200 mg daily in divided doses, and amantadine 100 mg twice daily, and 86 patients (placebo group) received interferon alfa-2b, ribavirin, and identical placebo. Treatment was discontinued at 24 weeks if patients had detectable HCV RNA by polymerase chain reaction (PCR). All patients were followed for 24 weeks after completion of treatment. The primary end point was undetectable HCV-RNA by PCR at 24 weeks (sustained viral clearance) after completion of treatment.>Results: At the end of treatment, HCV RNA clearance was seen in 32.9% of the amantadine group and 38.4% of the placebo group (p = 0.3). Sustained virological response was seen in 24.7% of the amantadine group and in 27.9% of the placebo group by intention to treat analysis; response rate was 30.4% and 34.8%, respectively, in those who completed 24 weeks of treatment. Poor response was seen in both groups among cirrhotics, African-Americans, genotype 1, and those with a higher viral load. By multivariate analysis, genotype 1, high viral load, and low serum albumin were the only predictors of poor response. Addition of amantadine to the standard regimen did not result in any unexpected side effects.>Conclusion: Response to triple therapy of interferon alfa, ribavirin, and amantadine was similar to standard therapy of interferon alfa and ribavirin. Our results suggest that amantadine has no role in the management of HCV.
机译:>背景和目标:在这项研究中,我们比较了三联疗法(干扰素α,利巴韦林和金刚烷胺)与标准疗法(干扰素α和利巴韦林)在未治疗的慢性丙型肝炎病毒( HCV)。>方法:在这项前瞻性,随机,双盲,安慰剂对照,多中心研究中,85例患者(金刚烷胺组)接受三剂干扰素α-2b的药物治疗,每周三百万次,共300万次,利巴韦林分剂量每天1000-1200 mg和金刚烷胺100 mg每天两次,有86例患者(安慰剂组)接受了干扰素α-2b,利巴韦林和相同的安慰剂。如果患者通过聚合酶链反应(PCR)检测到HCV RNA,则在24周时终止治疗。所有患者在治疗完成后均接受随访24周。主要终点是治疗完成后24周PCR(持续病毒清除率)检测不到的HCV-RNA。>结果:治疗结束时,金刚烷胺中32.9%的患者HCV RNA清除率组和安慰剂组的38.4%(p = 0.3)。通过治疗分析,金刚烷胺组和安慰剂组的病毒学应答分别为24.7%和27.9%。在完成24周治疗的患者中,缓解率分别为30.4%和34.8%。在肝硬化药,非裔美国人,基因型1和病毒载量较高的两组中,两组反应均较差。通过多变量分析,基因型1,高病毒载量和低血清白蛋白是不良反应的唯一预测因子​​。标准方案中添加金刚烷胺不会导致任何意外的副作用。>结论:对干扰素α,利巴韦林和金刚烷胺三联疗法的反应与干扰素α和利巴韦林的标准疗法相似。我们的结果表明,金刚烷胺在HCV的管理中没有作用。

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