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Peginterferon alfa-2b as monotherapy or in combination with lamivudine in patients with HBeAg-negative chronic hepatitis B: a randomised study

机译:聚乙二醇干扰素α-2b单药或联合拉米夫定治疗HBeAg阴性慢性乙型肝炎患者:一项随机研究

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Background The efficacy of pegylated interferon alfa-2b alone or in combination with lamivudine for the treatment of patients with hepatitis B e antigen (HBeAg) negative (-) chronic hepatitis B (CHB) is understudied. Material and Method One hundred twenty-six patients with HBeAg(-)chronic hepatitis B received pegylated interferon alfa-2b > or =1.5 micro g/kg/wk for 48 weeks. Ninety of those subjects were randomly selected to receive concomitant treatment with lamivudine 100 mg/d. The coprimary end points were the subjects' virologic (hepatitis B virus deoxyribonucleic acid [HBV DNA] <60 IU/mL) and biochemical (normalization of alanine aminotransferase levels) responses 24 weeks after treatment cessation. Results The scores for necroinflammatory activity and fibrosis in patients randomly assigned to receive monotherapy were statistically significantly lower than those in patients receiving combination therapy. HBV DNA levels were statistically significantly higher and alanine aminotransferase levels were statistically significantly lower in patients receiving monotherapy than in those receiving combination therapy. Virologic responses in the monotherapy and combination therapy groups were similar at weeks 48 and 72 (59.1 vs 42.9%). The biochemical response at week 72 was also similar in the treatment groups. The results of multiple regression analysis showed that the virologic response at week 72 was independently correlated with the pegylated interferon alfa-2b dose and that the biochemical response was independently correlated with necroinflammatory activity, the pegylated interferon alfa-2b dose, and lamivudine therapy. Conclusions These data support the use of pegylated interferon alfa-2b in patients with HBeAg(-) chronic hepatitis B; however, the concomitant use of lamivudine produced no additional clinical benefit.
机译:背景技术研究了单独的聚乙二醇化干扰素α-2b或与拉米夫定联用治疗乙型肝炎e抗原(HBeAg)阴性(-)慢性乙型肝炎(CHB)的疗效。材料和方法126例HBeAg(-)慢性乙型肝炎患者接受了48周的聚乙二醇化干扰素alfa-2b≥1.5微克/千克/周。随机选择其中的90名受试者接受拉米夫定100 mg / d的伴随治疗。共同的主要终点是受试者在停止治疗后24周的病毒学应答(乙肝病毒脱氧核糖核酸[HBV DNA] <60 IU / mL)和生化应答(丙氨酸氨基转移酶水平正常化)。结果随机分配接受单药治疗的患者的炎性炎症和纤维化评分明显低于接受联合治疗的患者。与接受联合治疗的患者相比,接受单一治疗的患者的HBV DNA水平在统计学上显着较高,而丙氨酸转氨酶水平在统计学上显着较低。在第48周和第72周,单一疗法和联合疗法组的病毒学应答相似(59.1 vs 42.9%)。治疗组在第72周的生化反应也相似。多元回归分析的结果表明,第72周的病毒学应答与聚乙二醇化干扰素al-2b剂量独立相关,生化应答与坏死性炎症活性,聚乙二醇化干扰素al-2b剂量和拉米夫定治疗独立相关。结论这些数据支持聚乙二醇化干扰素α-2b在慢性乙型肝炎(HBeAg)患者中的应用。然而,拉米夫定的同时使用并没有产生额外的临床益处。

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