Robins Gayle W, Scott Lesley J, Keating Gillian M
Adis International Limited, Auckland, New Zealand.
Drugs. 2005;65(6):809-25. doi: 10.2165/00003495-200565060-00010.
Subcutaneous peginterferon-alpha-2a (40kD) [Pegasys] is an effective and reasonably well tolerated treatment for the management of patients with hepatitis B e antigen (HBeAg)-negative or -positive chronic hepatitis B. It was significantly more effective than lamivudine monotherapy at inducing sustained virological response and ALT normalisation in both HBeAg-negative and -positive patients. Notably, the addition of lamivudine to peginterferon-alpha-2a (40kD) conferred no additional benefit versus peginterferon-alpha-2a (40kD) monotherapy. Moreover, in HBeAg-positive patients significantly more peginterferon-alpha-2a (40kD) recipients experienced HBeAg seroconversion than lamivudine recipients. The position of peginterferon-alpha-2a (40kD) relative to other treatment options remains to be fully determined. In the meantime, this agent appears to be a valuable new option for the management of patients with HBeAg-negative or -positive chronic hepatitis B.
皮下注射聚乙二醇化干扰素α-2a(40kD)[派罗欣]是一种治疗乙型肝炎e抗原(HBeAg)阴性或阳性慢性乙型肝炎患者的有效且耐受性良好的疗法。在诱导HBeAg阴性和阳性患者持续病毒学应答及ALT正常化方面,它显著优于拉米夫定单药治疗。值得注意的是,在聚乙二醇化干扰素α-2a(40kD)基础上加用拉米夫定与聚乙二醇化干扰素α-2a(40kD)单药治疗相比并无额外益处。此外,在HBeAg阳性患者中,接受聚乙二醇化干扰素α-2a(40kD)治疗的患者发生HBeAg血清学转换的比例显著高于接受拉米夫定治疗的患者。聚乙二醇化干扰素α-2a(40kD)相对于其他治疗选择的地位仍有待充分确定。与此同时,该药物似乎是治疗HBeAg阴性或阳性慢性乙型肝炎患者的一种有价值的新选择。