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Impact of pegylated interferon alpha-2B and ribavirin on hepatic fibrosis in liver transplant patients with recurrent hepatitis C: an open-label series.

机译:聚乙二醇化干扰素α-2B和利巴韦林对复发性丙型肝炎肝移植患者肝纤维化的影响:开放标签系列。

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Background: Patients with recurrent hepatitis C virus (HCV) are often treated with interferon-based therapy in an attempt to eradicate HCV and prevent cirrhosis requiring retransplantation. We describe our experience with pegylated interferon and ribavirin and the impact of this therapy on hepatic fibrosis. Methods: Patients were treated with pegylated interferon alpha-2b 1.5 mcg/kg/week and ribavirin 800 mg/day for 6-12 months according to genotype. HCV ribonucleic acid (HCV RNA) was repeated at 3 months, end of treatment (EOT) and 6 months after EOT for patients HCV RNA negative at EOT. Liver biopsies were performed prior to treatment and at EOT. Results: Thirty nine patients were eligible. Twenty two completed treatment and 17 (43.6%) were intolerant. Eleven of 22 (50%) patients who completed treatment developed sustained viral response (SVR). Two patients intolerant to treatment also developed SVR. Serial biopsies were performed in 17 patients and refused in five. Improved fibrosis scores were present in four patients (non-responders, n=2), unchanged in 10 (non-responders, n=4), and worse in three (all non-responders). Conclusions: Side effects are an important limiting factor in recurrent HCV treatment with SVR only 33.3% in an intention-to-treat analysis. However, improved or stable fibrosis scores were also demonstrated in 66.7% of non-responders. This suggests failure to eradicate HCV should not necessarily lead to treatment discontinuation as a subgroup of patients may benefit from maintenance therapy.
机译:背景:患有复发性丙型肝炎病毒(HCV)的患者经常接受基于干扰素的治疗,以根除HCV并预防需要移植的肝硬化。我们描述了我们在聚乙二醇化干扰素和利巴韦林方面的经验以及该疗法对肝纤维化的影响。方法:根据基因型,患者接受聚乙二醇干扰素α-2b1.5 mcg / kg /周和利巴韦林800 mg /天的治疗,持续6-12个月。对于在EOT阴性的HCV RNA患者,在治疗结束(EOT)的3个月和EOT后6个月重复HCV核糖核酸(HCV RNA)。在治疗前和EOT进行肝活检。结果:39名患者符合条件。完成治疗的有22例,其中17例(43.6%)不耐受。完成治疗的22名患者中有11名(50%)出现了持续病毒应答(SVR)。两名不耐治疗的患者也发生了SVR。连续活检17例,拒绝5例。改善的纤维化评分在四名患者中(无反应者,n = 2),在10名患者中无变化(无反应者,n = 4),而在三名患者中(所有无反应者)则更差。结论:在意向性治疗分析中,副作用是复发性HCV治疗SVR仅33.3%的重要限制因素。但是,在66.7%的无反应者中也显示出改善或稳定的纤维化评分。这表明未能根除HCV并不一定会导致治疗中断,因为亚组患者可能会受益于维持治疗。

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