Peginterferon alfa-2a in patients with chronic hepatitis C and cirrhosis

被引:648
作者
Heathcote, EJ
Shiffman, ML
Cooksley, WGE
Dusheiko, GM
Lee, SS
Balart, L
Reindollar, R
Reddy, RK
Wright, TL
Lin, A
Hoffman, J
De Pamphilis, J
机构
[1] Toronto Western Hosp, Univ Hlth Network, Dept Med, Toronto, ON M5T 2S8, Canada
[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Med, Hepatol Sect, Richmond, VA 23298 USA
[3] Royal Brisbane Hosp, Dept Med, Brisbane, Qld 4029, Australia
[4] Royal Free Hosp, Dept Med, Dept Clin Res, London NW3 2QG, England
[5] Heritage Med Res Clin, Dept Med, Calgary, AB, Canada
[6] Louisiana State Univ, Hlth Sci Ctr, Dept Med, New Orleans, LA USA
[7] Carolinas Ctr Liver Dis, Dept Med, Charlotte, NC USA
[8] Univ Miami, Sch Med, Dept Med, Ctr Liver Dis, Miami, FL USA
[9] Vet Affairs Med Ctr, Dept Med, Gastroenterol Unit, San Francisco, CA 94121 USA
[10] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
关键词
D O I
10.1056/NEJM200012073432302
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Chronic hepatitis C virus (HCV) infection in patients with cirrhosis is difficult to treat. In patients with chronic hepatitis C but without cirrhosis, once-weekly administration of interferon modified by the attachment of a 40-kd branched-chain polyethylene glycol moiety (peginterferon alfa-2a) is more efficacious than a regimen of unmodified interferon. We examined the efficacy and safety of peginterferon alfa-2a in patients with HCV-related cirrhosis or bridging fibrosis. Methods: We randomly assigned 271 patients with cirrhosis or bridging fibrosis to receive subcutaneous treatment with 3 million units of interferon alfa-2a three times weekly (88 patients), 90 microg of peginterferon alfa-2a once weekly (96), or 180 microg of peginterferon alfa-2a once weekly (87). Treatment lasted 48 weeks and was followed by a 24-week follow-up period. We assessed efficacy by measuring HCV RNA and alanine aminotransferase and by evaluating liver-biopsy specimens. A histologic response was defined as a decrease of at least 2 points on the 22-point Histological Activity Index. Results: In an intention-to-treat analysis, HCV RNA was undetectable at week 72 in 8 percent, 15 percent, and 30 percent of the patients treated with interferon alfa-2a and with 90 microg and 180 microg of peginterferon alfa-2a, respectively (P=0.001 for the comparison between 180 microg of peginterferon alfa-2a and interferon alfa-2a). At week 72, alanine aminotransferase concentrations had normalized in 15 percent, 20 percent, and 34 percent of patients, respectively (P=0.004 for the comparison between 180 microg of peginterferon alfa-2a and interferon alfa-2a). In the subgroup of 184 patients with paired liver-biopsy specimens, the rates of histologic response at week 72 were 31 percent, 44 percent, and 54 percent, respectively (P=0.02 for the comparison between 180 microg of peginterferon alfa-2a and interferon alfa-2a). All three treatments were similarly tolerated. Conclusions: In patients with chronic hepatitis C and cirrhosis or bridging fibrosis, 180 microg of peginterferon alfa-2a administered once weekly is significantly more effective than 3 million units of standard interferon alfa-2a administered three times weekly. (N Engl J Med 2000;343:1673-80.) (C) 2000, Massachusetts Medical Society.
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收藏
页码:1673 / 1680
页数:8
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