A randomized, placebo-controlled study to evaluate the efficacy of 12-month famciclovir treatment in patients with chronic hepatitis B e antigen-positive hepatitis B

被引:55
作者
de Man, RA
Marcellin, P
Habal, F
Desmond, P
Wright, T
Rose, T
Jurewicz, R
Young, C
机构
[1] Univ Rotterdam Hosp, Dept Hepatogastroenterol, NL-3000 CA Rotterdam, Netherlands
[2] Hop Beaujon, Clichy, France
[3] Toronto Gen Hosp, Toronto, ON, Canada
[4] St Vincent Hosp, Fitzroy, Vic, Australia
[5] Vet Adm Med Ctr, San Francisco, CA 94121 USA
[6] Middlemore Hosp, Auckland 6, New Zealand
[7] SmithKline Beecham Pharmaceut, Collegeville, PA USA
关键词
D O I
10.1053/jhep.2000.9407
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We conducted a randomized, placebo-controlled clinical study evaluating famciclovir (500 mg 3 times daily and 1.5 g once daily) for 1 year (6 months post-treatment follow-up) in patients with chronic hepatitis B e antigen (HBeAg)-positive hepatitis B virus (HBV) infection. The study was conducted in 80 centers in North America, Europe, and Australia/New Zealand, A total of 417 patients with histologically documented chronic hepatitis B (histologic activity index [HAI] 9.5-11.0) received famciclovir (500 mg 3 times daily or 1.5 g once daily) or placebo. Famciclovir 500 mg 3 times daily significantly reduced HBV DNA and median HAI scores versus placebo. By week 8, median HBV DNA decreased from 1,645 to 283 MEq/mL (famciclovir 500 mg 3 times daily) and from 1,147 to 304 MEq/mL (famciclovir 1.5 g once daily), while increasing for placebo (1,617 to 1,685 MEq/mL). Median change in HBV DNA at the end of therapy was -76% (famciclovir 500 mg 3 times daily; P < .01) and -60% (famciclovir 1.5 g once daily; P = .25) versus -37% for placebo. Median change in HAI was -1.5 points (famciclovir 500 mg 3 times daily; P = .02) and -1.0 point (famciclovir 1.5 g once daily; P = .35) and zero for placebo. Fifty percent of patients receiving famciclovir 500 mg 3 times daily (P = .07) and 43% receiving 1.5 g once daily (P = .41) experienced greater than or equal to 2 points improvement in HAI versus 37% for placebo. Nine percent of patients treated with famciclovir 500 mg 3 times daily underwent anti-HBeAg sero-conversion with undetectable HBV DNA at end of follow-up versus 3% in the placebo group (P = .05). Famciclovir was well tolerated; the incidence of post-treatment alanine transaminase (ALT) elevations was comparable with placebo. In conclusion, famciclovir 500 mg 3 times daily gave modest suppression of viral replication, but translated into significant histologic improvement in median HAI score at 1 year.
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页码:413 / 417
页数:5
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