Piratvisuth Teerha, Marcellin Patrick, Popescu Matei, Kapprell Hans-Peter, Rothe Vivien, Lu Zhi-Meng
NKC Institute of Gastroenterology and Hepatology, Songklanagarind Hospital, Prince of Songkla University, Hat Yai, Thailand.
Service d'Hépatologie U773-CRB3, Hôpital Beaujon, University of Paris, Clichy, France.
Hepatol Int. 2013 Jun;7(2):429-36. doi: 10.1007/s12072-011-9280-0. Epub 2011 Jun 24.
Patients with hepatitis B e antigen (HBeAg)-positive chronic hepatitis B, who achieve HBeAg seroconversion 6 months after completing 48 weeks of peginterferon alfa-2a therapy, have an increased chance of clearing hepatitis B surface antigen (HBsAg) during long-term treatment-free follow-up. This analysis aimed to determine whether HBsAg quantification during treatment could be used to identify posttreatment response.
Patients (n = 399) treated with peginterferon alfa-2a (180 μg/week) alone or in combination with lamivudine (100 mg/day) for 48 weeks during a large, randomized study were included in this retrospective analysis. Receiver-operating characteristic analyses were used to identify baseline and on-treatment HBsAg levels associated with response (HBeAg seroconversion 6 months posttreatment).
Baseline HBsAg levels were lower in patients achieving posttreatment response than in nonresponders (3.97 and 4.21 IU/mL, respectively, p = 0.039). Two baseline HBsAg cutoff levels (5,000 and 50,000 IU/mL) provided a positive predictive value of 42% and a negative predictive value of 77%. HBsAg decline was significantly greater during and posttreatment in responders than in nonresponders (p < 0.0001). HBeAg seroconversion rates 6 months posttreatment were significantly higher in patients with HBsAg < 1,500 IU/mL at weeks 12 and 24 (56.7 and 54.4%, respectively) versus patients with HBsAg 1,500-20,000 IU/mL (32.3 and 26.1%, respectively) or HBsAg < 20,000 IU/mL (16.3 and 15.4%, respectively) (all p < 0.0001 and <0.0001).
HBsAg levels at baseline strongly associated with posttreatment response were not identified. Low HBsAg levels during peginterferon alfa-2a therapy were associated with high rates of posttreatment response. On-treatment HBsAg quantification may, therefore, help guide patient management in the future.
接受聚乙二醇干扰素α-2a治疗48周后6个月实现乙肝e抗原(HBeAg)血清学转换的HBeAg阳性慢性乙型肝炎患者,在长期停药随访期间清除乙肝表面抗原(HBsAg)的几率增加。本分析旨在确定治疗期间的HBsAg定量是否可用于识别治疗后反应。
在一项大型随机研究中,单独使用聚乙二醇干扰素α-2a(180μg/周)或与拉米夫定(100mg/天)联合使用48周的患者(n = 399)纳入本回顾性分析。采用受试者操作特征分析来确定与反应(治疗后6个月HBeAg血清学转换)相关的基线和治疗期间HBsAg水平。
治疗后有反应的患者基线HBsAg水平低于无反应者(分别为3.97和4.21IU/mL,p = 0.039)。两个基线HBsAg临界值(5000和50000IU/mL)的阳性预测值为42%,阴性预测值为77%。有反应者在治疗期间和治疗后的HBsAg下降幅度明显大于无反应者(p < 0.0001)。在第12周和第24周时HBsAg < 1500IU/mL的患者治疗后6个月的HBeAg血清学转换率显著高于HBsAg为1500 - 20000IU/mL的患者(分别为56.7%和54.4%)或HBsAg < 20000IU/mL的患者(分别为16.3%和15.4%)(所有p < 0.0001和<0.0001)。
未确定与治疗后反应密切相关的基线HBsAg水平。聚乙二醇干扰素α-2a治疗期间低HBsAg水平与高治疗后反应率相关。因此,治疗期间的HBsAg定量可能有助于未来指导患者管理。