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聚乙二醇干扰素 α-2a(40kD):在慢性乙型肝炎中的应用评价。

Peginterferon-alpha-2a (40 kD): A review of its use in chronic hepatitis B.

机构信息

Adis, a Wolters Kluwer Business, Auckland, New Zealand.

出版信息

Drugs. 2009;69(18):2633-60. doi: 10.2165/11203660-000000000-00000.

Abstract

Peginterferon-alpha-2a (40 kD) [Pegasys] comprises an inert, branched, 40 kD polyethylene glycol (PEG) moiety attached to interferon-alpha-2a. Subcutaneous peginterferon-alpha-2a (40 kD) is indicated for the treatment of adults with hepatitis B e antigen (HBeAg)-positive or -negative chronic hepatitis B who have compensated liver disease with evidence of viral replication and hepatic inflammation. Subcutaneous peginterferon-alpha-2a (40 kD) has antiviral and immunomodulatory properties and a convenient once-weekly administration schedule. Forty-eight weeks of therapy with peginterferon-alpha-2a (40 kD) with or without lamivudine was more effective than lamivudine alone in achieving a sustained response in patients with HBeAg-positive or -negative chronic hepatitis B. A long-term follow-up study in patients with HBeAg-positive disease who received peginterferon-alpha-2a (40 kD) monotherapy revealed an HBeAg seroconversion rate of 42%, 1 year after the end of treatment. A long-term follow-up study in patients with HBeAg-negative disease who received peginterferon-alpha-2a (40 kD) with or without lamivudine revealed hepatitis B surface antigen (HBsAg) clearance in 12% of patients and inactive chronic hepatitis B in 17% of patients, 5 years after the end of treatment. Various predictors of response may be useful in terms of identifying patients who may be candidates for shorter or longer peginterferon-alpha-2a (40 kD) treatment durations. For example, quantifying serum HBeAg (in HBeAg-positive disease) and HBsAg levels during therapy may be useful. Adverse events typical of the influenza-like symptoms seen with alpha-interferons occurred more frequently in patients with chronic hepatitis B receiving peginterferon-alpha-2a (40 kD) with or without lamivudine than in those receiving lamivudine alone. In conclusion, peginterferon-alpha-2a (40 kD) is a valuable option for the first-line treatment of HBeAg-negative or -positive chronic hepatitis B.

摘要

聚乙二醇干扰素 alpha-2a(40kD)[派罗欣]由惰性分支的 40kD 聚乙二醇(PEG)部分与干扰素 alpha-2a 连接组成。皮下注射用聚乙二醇干扰素 alpha-2a(40kD)适用于治疗代偿性肝脏疾病且有病毒复制和肝脏炎症证据的 HBeAg 阳性或阴性慢性乙型肝炎成人患者。皮下注射用聚乙二醇干扰素 alpha-2a(40kD)具有抗病毒和免疫调节特性,且每周给药 1 次给药方案方便。聚乙二醇干扰素 alpha-2a(40kD)联合或不联合拉米夫定治疗 48 周比拉米夫定单药治疗更能有效实现 HBeAg 阳性或阴性慢性乙型肝炎患者的持续应答。在 HBeAg 阳性疾病患者中进行的聚乙二醇干扰素 alpha-2a(40kD)单药治疗长期随访研究显示,在治疗结束后 1 年时,HBeAg 血清学转换率为 42%。在 HBeAg 阴性疾病患者中进行的聚乙二醇干扰素 alpha-2a(40kD)联合或不联合拉米夫定治疗长期随访研究显示,在治疗结束后 5 年时,12%的患者出现乙型肝炎表面抗原(HBsAg)清除,17%的患者出现非活动慢性乙型肝炎。各种应答预测因子可能有助于识别可能适合接受较短或较长聚乙二醇干扰素 alpha-2a(40kD)治疗时间的患者。例如,在治疗期间定量检测血清 HBeAg(在 HBeAg 阳性疾病中)和 HBsAg 水平可能有用。与单独接受拉米夫定治疗的慢性乙型肝炎患者相比,接受聚乙二醇干扰素 alpha-2a(40kD)联合或不联合拉米夫定治疗的患者更常出现类似流感的干扰素 alpha 相关症状。总之,聚乙二醇干扰素 alpha-2a(40kD)是 HBeAg 阴性或阳性慢性乙型肝炎一线治疗的一个有价值的选择。

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