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Treatment of chronic hepatitis C in patients unresponsive to interferon. Interest of re-treatment combining interferon induction therapy and ribavirin (a multicenter pilot study)

机译:对干扰素无反应的患者治疗慢性丙型肝炎。结合干扰素诱导治疗和利巴韦林的再治疗的兴趣(多中心试验研究)

摘要

AimAbout 45% of patients with chronic hepatitis C are unresponsive to the present reference treatment combining pegelated interferon plus ribavirin; before pegylated interferon was available the non-response rate was around 60%. This open multicenter pilot study, initiated before pegylated interferon became available, was designed to evaluate, in patients unresponsive to interferon monotherapy, the rate of biological and virological response and side-effects of the ribivirin- alpha 2b interferon combination.MethodsThe combination protocol was ribavirin (1 to 1.2 g/d) plus alpha 2b interferon at induction doses (9 MU/d the first week; 4.5 MU/d the eleven following weeks; 3 MU/2 days the 36 following weeks).ResultsAmong the 27 included patients, 17 (63%) were viremia-negative (PCR) after 12 weeks of treatment, 9 (33%) were complete responders (undetectable viremia and normal transaminases) at the end of treatment (48 weeks) and of follow-up (72 weeks). Patients with non-1, non-4 genotypes who derived full benefit from this therapeutic strategy (6/7 (86%) were complete responders: 4/5 with genotype 3 and 2/2 with genotype 5). Quality-of-life was impaired during treatment, especially during the first 12 weeks of high-dose interferon therapy.ConclusionWhile waiting for new therapeutic possibilities, these good results suggest interferon induction at the beginning of treatment remains a valid option.
机译:目的约有45%的慢性丙型肝炎患者对目前的参考治疗无效,该治疗采用干扰素加利巴韦林联合治疗;在获得聚乙二醇化干扰素之前,无反应率约为60%。这项开放的多中心试验研究始于聚乙二醇化干扰素可用之前,旨在评估对干扰素单药治疗无反应的患者的病毒学和病毒学应答率以及利巴韦林-α2b干扰素联合用药的副作用。 (1至1.2 g / d)加α2b干扰素的诱导剂量(第一周9 MU / d;接下来11周4.5 MU / d;接下来36周3 MU / 2天)结果在27名患者中,治疗12周后17例(63%)为病毒血症阴性(PCR),在治疗结束(48周)和随访(72周)中有9例(33%)为完全缓解(无法检测到病毒血症和正常转氨酶) )。从这种治疗策略中获得全部益处的非1,非4基因型患者(6/7(86%)是完全缓解者:基因型3为4/5,基因型5为2/2)。在治疗期间,尤其是在大剂量干扰素治疗的前12周期间,生活质量受到损害。结论在等待新的治疗方法时,这些良好的结果表明在治疗开始时诱导干扰素仍然是有效的选择。

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