首页> 外文期刊>Journal of interferon and cytokine research: The official journal of the International Society for Interferon and Cytokine Research >The efficacy of a Hansenula-derived 20 kDa pegylated interferon alpha-2a in the treatment of genotype 4 chronic hepatitis C
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The efficacy of a Hansenula-derived 20 kDa pegylated interferon alpha-2a in the treatment of genotype 4 chronic hepatitis C

机译:汉逊酵母来源的20 kDa聚乙二醇干扰素α-2a在治疗基因型4型慢性丙型肝炎中的功效

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Pending the emergence and approval of an effective interferon-free regimen, pegylated interferon will remain an integral part of the treatment of genotype 4 hepatitis C virus (HCV). A new 20 kDa pegylated interferon has been developed in a cost-saving fungal-based system and is commercialized in Egypt at a quarter to a third of the price of conventional pegylated interferon. We hereby test the efficacy and safety of this novel cost-saving interferon. One hundred ninety-three consecutive treatment-naive patients with genotype 4 HCV were treated using the following regimen: subcutaneous 20 kDa pegylated interferon 160 μg once weekly plus oral ribavirin 1,000 or 1,200 mg daily (based on body weight <75 kg or ≥75 kg, respectively) for 48 weeks. A sustained virological response (SVR) of 51% was achieved. Interim responses included rapid virological response (RVR): 54%, early virological response (EVR): 78% (complete EVR: 71%, partial EVR: 7%), and end of treatment response: 63%. The most common adverse events were flu-like symptoms, dyspepsia, anorexia, and pruritus. Treatment-related serious adverse events were encountered in only 2 patients (1%). Discontinuation of treatment due to adverse events occurred in only 13 patients (7%). Multiple logistic regression analyses revealed the following factors as predictors of SVR: RVR (P<0.001), alpha- fetoprotein
机译:在有效的无干扰素治疗方案出现和批准之前,聚乙二醇化干扰素仍将是基因4型丙型肝炎病毒(HCV)治疗的组成部分。在节省成本的基于真菌的系统中开发了一种新的20 kDa聚乙二醇化干扰素,并在埃及商业化,价格为传统聚乙二醇化干扰素的四分之一至三分之一。我们在此测试这种新型节省成本的干扰素的功效和安全性。使用以下方案治疗了193名连续接受初治的4型HCV患者:皮下注射20 kDa聚乙二醇化干扰素160μg,每周一次,口服口服利巴韦林1,000或1,200 mg(基于体重<75 kg或≥75kg) ),持续48周。达到了51%的持续病毒学应答(SVR)。临时反应包括快速病毒学应答(RVR):54%,早期病毒学应答(EVR):78%(完全EVR:71%,部分EVR:7%),治疗结束应答:63%。最常见的不良事件是流感样症状,消化不良,厌食和瘙痒。仅2名患者(1%)遇到了与治疗相关的严重不良事件。因不良事件而终止治疗的仅13例患者(7%)。多项logistic回归分析显示,以下因素可作为SVR的预测指标:RVR(P <0.001),甲胎蛋白<正常上限(ULN)(P = 0.007)和早期生化反应(丙氨酸转氨酶

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