Perrillo Robert P, Lai Ching-Lung, Liaw Yun-Fan, Dienstag Jules L, Schiff Eugene R, Schalm Solko W, Heathcote E Jenny, Brown Nathaniel A, Atkins Mark, Woessner Mary, Gardner Stephen D
Section of Gastroenterology and Hepatology, Ochsner Clinic Foundation, 1514 Jefferson Highway, New Orleans, LA 70121, USA.
Hepatology. 2002 Jul;36(1):186-94. doi: 10.1053/jhep.2002.34294.
Elevated alanine transaminase (ALT) levels and low serum hepatitis B virus (HBV) DNA predict a higher likelihood of hepatitis B e antigen (HBeAg) loss in patients with chronic hepatitis B treated with interferon. Predictors of HBeAg loss in patients treated with lamivudine are not known. The objective of this analysis of 4 lamivudine-controlled Phase III trials was to determine patient-dependent or laboratory variables that predict HBeAg loss. Predictors of HBeAg loss in patients treated with interferon, lamivudine plus interferon, or placebo are also described. A total of 805 adults with chronic hepatitis B were treated either with lamivudine (n = 406), matching placebo (n = 196), interferon (n = 68), or the combination of lamivudine plus interferon (n = 135). Demographic and baseline disease characteristics were used in stepwise multivariate analyses to identify features that were predictive of lamivudine-induced HBeAg loss. HBeAg loss correlated with increased pretreatment ALT levels in all groups. The rate of HBeAg loss was highest among patients with pretreatment ALT levels greater than 5 times the upper limit of normal (ULN) and was most pronounced in the lamivudine group (56%). Multivariate modeling indicated that elevated baseline ALT levels (P <.001) and histologic activity index (HAI) score (P <.001) were important predictors of HBeAg loss in response to lamivudine. The effect of pretreatment ALT levels on HBeAg loss was similar for Asians and Caucasians. In conclusion, elevated pretreatment ALT levels and/or active histologic disease were the most important predictors of lamivudine-induced HBeAg loss. Asians and Caucasians had similar rates of response to lamivudine at comparable ALT levels.
谷丙转氨酶(ALT)水平升高和血清乙肝病毒(HBV)DNA水平低预示着接受干扰素治疗的慢性乙型肝炎患者出现乙肝e抗原(HBeAg)转阴的可能性更高。对于接受拉米夫定治疗的患者,HBeAg转阴的预测因素尚不清楚。本分析对4项拉米夫定对照的III期试验进行,目的是确定预测HBeAg转阴的患者相关或实验室变量。还描述了接受干扰素、拉米夫定加干扰素或安慰剂治疗的患者中HBeAg转阴的预测因素。共有805例慢性乙型肝炎成人患者接受了拉米夫定(n = 406)、匹配的安慰剂(n = 196)、干扰素(n = 68)或拉米夫定加干扰素联合治疗(n = 135)。在逐步多变量分析中使用人口统计学和基线疾病特征来识别预测拉米夫定诱导HBeAg转阴的特征。所有组中HBeAg转阴均与治疗前ALT水平升高相关。治疗前ALT水平大于正常上限(ULN)5倍的患者中HBeAg转阴率最高,在拉米夫定组中最为明显(56%)。多变量建模表明,基线ALT水平升高(P <.001)和组织学活动指数(HAI)评分(P <.001)是拉米夫定治疗后HBeAg转阴的重要预测因素。亚洲人和高加索人中,治疗前ALT水平对HBeAg转阴的影响相似。总之,治疗前ALT水平升高和/或组织学疾病活动是拉米夫定诱导HBeAg转阴的最重要预测因素。在相当的ALT水平下,亚洲人和高加索人对拉米夫定的反应率相似。