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Randomised, double-blind, placebo-controlled trial of interferon alpha-2b with and without ribavirin for chronic hepatitis C. The Swedish Study Group (see comments)

机译:干扰素α-2b联合或不联合利巴韦林治疗慢性丙型肝炎的随机,双盲,安慰剂对照试验。瑞典研究小组(参见评论)

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BACKGROUND: Pilot studies suggested that more patients with chronic hepatitis C virus (HCV) infection had a sustained virological response when treated with the combination of interferon alpha-2b and ribavirin than with interferon alpha-2b alone. We investigated the biochemical and virological responses and safety of treatment with interferon alpha-2b and ribavirin compared with interferon alpha-2b alone. METHODS: In this double-blind trial 100 patients were randomly assigned to treatment with interferon alpha-2b (3 MU three times a week) in combination with ribavirin (1000 or 1200 mg per day) or placebo for 24 weeks and then followed up for a further 24 weeks. A further follow-up was done 1 year after active treatment stopped. The primary endpoint was the sustained virological response, defined as no detectable HCV RNA by PCR at both week 24 and week 48. Retrospectively, the baseline HCV-RNA load was analysed as a predictor of a sustained virological response. Data were analysed by intention to treat. FINDINGS: 18 (36%) of the 50 patients in the interferon alpha-2b and ribavirin group had a sustained virological response compared with nine (18%) of the 50 patients in the interferon alpha-2b and placebo group (p = 0.047). At the 1 year follow-up the proportion of patients with a virological response was greater in the interferon alpha-2b and ribavirin group than the interferon alpha-2b and placebo group (42 vs 20%, p = 0.03), respectively. More patients with baseline HCV-RNA concentrations greater than 3 x 10(6) genome equivalents (Eq) per mL had a sustained response with interferon alpha-2b and ribavirin than with interferon alpha-2b and placebo (12/29 vs 1/26, p = 0.009), whereas the sustained response did not differ between the two treatment groups for HCV-RNA amounts less than 3 x 10(6) Eq per mL (6/21 vs 8/24, p = 0.67), respectively. INTERPRETATION: More patients with chronic hepatitis C have a sustained virological response with interferon alpha-2b and ribavirin than with only interferon alpha-2b treatment. We suggest that patients with high HCV-RNA loads should be treated with interferon alpha-2b and ribavirin.
机译:背景:初步研究表明,与单独使用干扰素α-2b联合使用干扰素α-2b和利巴韦林联合治疗时,更多的慢性丙型肝炎病毒(HCV)感染患者具有持续的病毒学应答。我们调查了干扰素α-2b和利巴韦林与单独的干扰素α-2b相比的生化和病毒学应答以及治疗的安全性。方法:在该双盲试验中,将100例患者随机分配接受干扰素α-2b(每周3次,每天3 MU)联合利巴韦林(每天1000或1200 mg)或安慰剂治疗24周,然后随访再过24周。积极治疗停止后一年进行了进一步的随访。主要终点是持续的病毒学应答,定义为在第24周和第48周均未通过PCR检测到HCV RNA。回顾性地,分析了基线HCV-RNA负荷作为持续病毒学应答的预测因子。按意向分析数据。结果:干扰素α-2b和利巴韦林组的50例患者中有18例(36%)具有持续的病毒学应答,而干扰素α-2b和安慰剂组的50例患者中有九例(18%)(p = 0.047) 。在1年的随访中,干扰素α-2b和利巴韦林组中具有病毒学应答的患者比例分别大于干扰素α-2b和安慰剂组(42%vs 20%,p = 0.03)。基线HCV-RNA浓度高于每毫升3 x 10(6)基因组当量(Eq)的患者对干扰素α-2b和利巴韦林的持续反应要比干扰素α-2b和安慰剂的持续反应高(12/29 vs 1/26 ,p = 0.009),而两个治疗组的HCV-RNA量分别少于3 x 10(6)Eq / mL时,持续反应没有差异(分别为6/21与8/24,p = 0.67)。解释:与仅使用干扰素α-2b治疗相比,更多的慢性丙型肝炎患者对干扰素α-2b和利巴韦林的持续病毒学应答。我们建议HCV-RNA负荷高的患者应使用干扰素α-2b和利巴韦林治疗。

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