A comparison of entecavir and lamivudine for HBeAg-positive chronic hepatitis B

Ting Tsung Chang, Robert G. Gish, Robert De Man, Adrian Gadano, José Sollano, You Chen Chao, Anna S. Lok, Kwang Hyub Han, Zachary Goodman, Jin Zhu, Anne Cross, Deborah DeHertogh, Richard Wilber, Richard Colonno, David Apelian

研究成果: Article同行評審

1258 引文 斯高帕斯(Scopus)


Background: Entecavir is a potent and selective guanosine analogue with significant activity against hepatitis B virus (HBV). Methods: In this phase 3, double-blind trial, we randomly assigned 715 patients with hepatitis B e antigen (HBeAg)-positive chronic hepatitis B who had not previously received a nucleoside analogue to receive either 0.5 mg of entecavir or 100 mg of lamivudine once daily for a minimum of 52 weeks. The primary efficacy end point was histologic improvement (a decrease by at least two points in the Knodell necro-inflammatory score, without worsening of fibrosis) at week 48. Secondary end points included a reduction in the serum HBV DNA level, HBeAg loss and seroconversion, and normalization of the alanine aminotransferase level. Results: Histologic improvement after 48 weeks occurred in 226 of 314 patients in the entecavir group (72 percent) and 195 of 314 patients in the lamivudine group (62 percent, P=0.009). More patients in the entecavir group than in the lamivudine group had undetectable serum HBV DNA levels according to a polymerase-chain-reaction assay (67 percent vs. 36 percent, P<0.001) and normalization of alanine aminotransferase levels (68 percent vs. 60 percent, P=0.02). The mean reduction in serum HBV DNA from baseline to week 48 was greater with entecavir than with lamivudine (6.9 vs. 5.4 log [on a base-10 scale] copies per milliliter, P<0.001). HBeAg seroconversion occurred in 21 percent of entecavir-treated patients and 18 percent of those treated with lamivudine (P=0.33). No viral resistance to entecavir was detected. Safety was similar in the two groups. Conclusions: Among patients with HBeAg-positive chronic hepatitis B, the rates of histologic, virologic, and biochemical improvement are significantly higher with entecavir than with lami vudine. The safety profile of the two agents is similar, and there is no evidence of viral resistance to entecavir.

頁(從 - 到)1001-1010
期刊New England Journal of Medicine
出版狀態Published - 2006 3月 9

All Science Journal Classification (ASJC) codes

  • 醫藥 (全部)


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