A one-year trial of lamivudine for chronic hepatitis B

Ching Lung Lai, Rong Nan Chien, Nancy W.Y. Leung, Ting Tsung Chang, Richard Guan, Dar In Tai, Keng Yeen Ng, Pui Chee Wu, Julie C. Dent, Judy Barber, Sally L. Stephenson, D. Fraser Gray

研究成果: Article同行評審

1800 引文 斯高帕斯(Scopus)

摘要

Background and Methods: In preliminary trials, lamivudine, an oral nucleoside analogue, has shown promise for the treatment of chronic hepatitis B. We conducted a one-year double-blind trial of lamivudine in 358 Chinese patients with chronic hepatitis B. The patients were randomly assigned to receive 25 mg of lamivudine (142 patients), 100 mg of lamivudine (143), or placebo (73) orally once daily. The patients underwent liver biopsies before entering the study and after completing the assigned treatment regimen. The primary end point was a reduction of at least two points in the Knodell necroinflammatory score. Results: Hepatic necroinflammatory activity improved by two points or more in 56 percent of the patients receiving 100 mg of lamivudine, 49 percent of those receiving 25 mg of lamivudine, and 25 percent of those receiving placebo (P<0.001 and P=0.001, respectively, for the comparisons of lamivudine treatment with placebo). Necroinflammatory activity worsened in 7 percent of the patients receiving 100 mg of lamivudine, 8 percent of those receiving 25 mg, and 26 percent of those receiving placebo. The 100mg dose of lamivudine was associated with a reduced progression of fibrosis (P=0.01 for the comparison with placebo) and with the highest rate of hepatitis B e antigen (HBeAg) seroconversion (loss of HBeAg, development of antibody to HBeAg, and undetectable HBV DNA) (16 percent), the greatest suppression of HBV DNA (98 percent reduction at week 52 as compared with the base-line value), and the highest rate of sustained normalization of alanine aminotransferase levels (72 percent). Ninety-six percent of the patients completed the study. The incidence of adverse events was similar in all groups, and there were few serious events. Conclusions: In a one-year study, lamivudine was associated with substantial histologic improvement in many patients with chronic hepatitis B. A daily dose of 100 mg was more effective than a daily dose of 25 mg.

原文English
頁(從 - 到)61-68
頁數8
期刊New England Journal of Medicine
339
發行號2
DOIs
出版狀態Published - 1998 7月 9

All Science Journal Classification (ASJC) codes

  • 一般醫學

指紋

深入研究「A one-year trial of lamivudine for chronic hepatitis B」主題。共同形成了獨特的指紋。

引用此