Jang Jeong Won, Bae Si Hyun, Choi Jong Young, Kim Chang Wook, Han Nam Ik, Han Jun Yeol, Choi Sang Wook, Yoon Seung Kew, Chung Kyu Won, Sun Hee Sik
Department of Internal Medicine and WHO Collaborating Center on Viral Hepatitis, College of Medicine, The Catholic University of Korea, Seoul, Korea.
J Gastroenterol Hepatol. 2006 Feb;21(2):384-91. doi: 10.1111/j.1440-1746.2005.04035.x.
Studies from hepatitis B virus endemic areas have shown less durable lamivudine-induced responses and have raised issues about the management of a post-treatment relapse.
From January 2000 to June 2004, all 51 patients (43 HBeAg-positive and eight HBeAg-negative) were retreated with lamivudine for at least 12 months. All had a post-treatment relapse after HBeAg responses (HBeAg loss/seroconversion) during the first therapy.
During retreatment, HBeAg seroconversion occurred more frequently in those patients with HBeAg seroconversion than in those with HBeAg loss alone during prior lamivudine therapy (P = 0.001). On multivariate analysis, prior HBeAg seroconversion and early virological response (EVR) (< or = 2 months of retreatment) independently predicted HBeAg seroconversion (P = 0.012 and P = 0.004, respectively). With regard to virological breakthrough, only the time to virological response (> 2 months of retreatment) remained significant (P = 0.048). Among the HBeAg-negative patients, virological breakthrough occurred in only one patient with a late virological response.
EVR is a major predictor in determining a favorable response to lamivudine retreatment. Our observations suggest that lamivudine retreatment will provide more therapeutic gains in those patients with a prior HBeAg seroconversion than in those with HBeAg loss alone.
来自乙肝病毒流行地区的研究显示,拉米夫定诱导的反应持久性较差,并引发了治疗后复发管理方面的问题。
2000年1月至2004年6月,对所有51例患者(43例HBeAg阳性和8例HBeAg阴性)再次使用拉米夫定治疗至少12个月。所有患者在首次治疗期间出现HBeAg反应(HBeAg消失/血清学转换)后均出现治疗后复发。
再次治疗期间,先前拉米夫定治疗期间发生HBeAg血清学转换的患者比仅发生HBeAg消失的患者更频繁地出现HBeAg血清学转换(P = 0.001)。多因素分析显示,先前的HBeAg血清学转换和早期病毒学应答(EVR)(再次治疗≤2个月)独立预测HBeAg血清学转换(分别为P = 0.012和P = 0.004)。关于病毒学突破,只有病毒学应答时间(再次治疗>2个月)仍然具有统计学意义(P = 0.048)。在HBeAg阴性患者中,仅1例病毒学应答延迟的患者发生了病毒学突破。
EVR是决定拉米夫定再次治疗良好反应的主要预测因素。我们的观察结果表明,与仅HBeAg消失的患者相比,拉米夫定再次治疗对先前有HBeAg血清学转换的患者将带来更多治疗益处。