Predictors of HBeAg loss after lamivudine treatment for chronic hepatitis B

被引:272
作者
Perrillo, RP
Lai, CL
Liaw, YF
Dienstag, JL
Schiff, ER
Schalm, SW
Heathcote, EJ
Brown, NA
Atkins, M
Woessner, M
Gardner, SD
机构
[1] Alton Ochsner Med Fdn & Ochsner Clin, Sect Gastroenterol & Hepatol, New Orleans, LA 70121 USA
[2] Glaxo Wellcome Inc, Res Triangle Pk, NC 27709 USA
[3] Glaxo Wellcome Res & Dev Ltd, Greenford, Middx, England
[4] Novirio Pharmaceut Inc, Cambridge, MA USA
[5] Toronto Western Hosp, Div Gastroenterol, Toronto, ON M5T 2S8, Canada
[6] Erasme Univ Hosp, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[7] Vet Affairs Med Ctr, Miami, FL 33125 USA
[8] Univ Miami, Med Ctr, Ctr Liver Dis, Miami, FL 33152 USA
[9] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[10] Massachusetts Gen Hosp, Liver Biliary Pancreas Ctr, Boston, MA 02114 USA
[11] Massachusetts Gen Hosp, Gastrointestinal Unit, Med Serv, Boston, MA 02114 USA
[12] Chang Gung Univ, Chang Gung Mem Hosp, Liver Res Unit, Taipei, Taiwan
[13] Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1053/jhep.2002.34294
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
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收藏
页码:186 / 194
页数:9
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