首页> 外文期刊>Alimentary pharmacology & therapeutics. >Clinical trial: a randomized trial of pegylated-interferon-alpha-2a plus ribavirin with or without amantadine in treatment-naive or relapsing chronic hepatitis C patients.
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Clinical trial: a randomized trial of pegylated-interferon-alpha-2a plus ribavirin with or without amantadine in treatment-naive or relapsing chronic hepatitis C patients.

机译:临床试验:初治或复发的慢性丙型肝炎患者接受聚乙二醇干扰素-α-2a加利巴韦林加金刚烷胺或不加金刚烷胺的随机试验。

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摘要

BACKGROUND: The combination therapy of pegylated-interferon-alpha2a plus ribavirin is considered as the standard of care for patients with chronic hepatitis C. A sustained viral response is obtained in 40-50% of naive patients with genotype 1 and in around 80% of naive patients with genotype 2 or 3. AIM: To assess whether amantadine, added to the conventional combination therapy, could improve the treatment efficacy. METHODS: In all, 630 patients (intent-to-treat population) with chronic hepatitis C were randomized into two groups: 316 patients (treatment group) received pegylated-interferon-alpha2a (180 microg once weekly) plus ribavirin (1000-1200 mg/daily) with amantadine (200 mg/daily); 314 patients (control group) received pegylated-interferon-alpha2a (180 microg once weekly) plus ribavirin (1000-1200 mg/daily) without amantadine. The duration of the treatment was 48 weeks for genotypes 1, 4, 5 and 6, and 24 weeks for genotypes 2 and 3. RESULTS: There was no statistically significant difference between treatments groups for any of the variables tested for. Subgroups of patients likely to take advantage of the addition of amantadine were not identified. CONCLUSIONS: This large study definitely excludes the role of amantadine in addition of conventional combination therapy in the treatment of chronic hepatitis C patients.
机译:背景:聚乙二醇化干扰素-α2a联合利巴韦林被认为是慢性丙型肝炎患者的标准治疗方法。40%至50%的1型基因天真患者和约80%的初次获得持续病毒应答初次使用基因型2或3的患者。目的:评估在传统联合疗法中添加金刚烷胺是否可以提高治疗效果。方法:总共将630例慢性丙型肝炎患者(意向性治疗)随机分为两组:316例患者(治疗组)接受聚乙二醇干扰素-α2a(每周一次180微克)加利巴韦林(1000-1200毫克) /天)与金刚烷胺(200毫克/天); 314名患者(对照组)接受了不含金刚烷胺的聚乙二醇干扰素-α2a(每周一次180微克)加利巴韦林(每天1000-1200毫克)的治疗。基因型1、4、5和6的治疗持续时间为48周,基因型2和3的治疗持续时间为24周。结果:治疗组之间的任何变量均无统计学差异。未发现可能利用金刚烷胺的患者亚组。结论:这项大型研究明确排除了金刚烷胺与常规联合治疗在慢性丙型肝炎患者治疗中的作用。

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