Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon

被引:317
作者
Di Bisceglie, Adrian M. [1 ]
Shiffman, Mitchell L. [2 ]
Everson, Gregory T. [3 ]
Lindsay, Karen L. [4 ]
Everhart, James E. [5 ]
Wright, Elizabeth C. [5 ]
Lee, William M. [6 ]
Lok, Anna S. [7 ]
Bonkovsky, Herbert L. [8 ]
Morgan, Timothy R. [9 ,10 ]
Ghany, Marc G. [5 ]
Morishima, Chihiro [11 ]
Snow, Kristin K. [12 ]
Dienstag, Jules L. [13 ,14 ]
机构
[1] St Louis Univ, Sch Med, Div Gastroenterol & Hepatol, Dept Internal Med, St Louis, MO 63110 USA
[2] Virginia Commonwealth Univ, Med Ctr, Richmond, VA USA
[3] Univ Colorado, Sch Med, Denver, CO 80202 USA
[4] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[5] NIDDKD, Bethesda, MD 20892 USA
[6] Univ Texas Dallas, SW Med Ctr, Dallas, TX USA
[7] Univ Michigan, Med Ctr, Ann Arbor, MI USA
[8] Univ Connecticut, Ctr Hlth, Farmington, CT USA
[9] Univ Calif Irvine, Irvine, CA USA
[10] Vet Affairs Long Beach Healthcare Syst, Long Beach, CA USA
[11] Univ Washington, Seattle, WA 98195 USA
[12] New England Res Inst, Watertown, MA 02172 USA
[13] Massachusetts Gen Hosp, Boston, MA 02114 USA
[14] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.1056/NEJMoa0707615
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In patients with chronic hepatitis C who do not have a response to antiviral treatment, the disease may progress to cirrhosis, liver failure, hepatocellular carcinoma, and death. Whether long-term antiviral therapy can prevent progressive liver disease in such patients remains uncertain. Methods: We conducted a randomized, controlled trial of peginterferon alfa-2a at a dosage of 90 microg per week for 3.5 years, as compared with no treatment, in 1050 patients with chronic hepatitis C and advanced fibrosis who had not had a response to previous therapy with peginterferon and ribavirin. The patients, who were stratified according to stage of fibrosis (622 with noncirrhotic fibrosis and 428 with cirrhosis), were seen at 3-month intervals and underwent liver biopsy at 1.5 and 3.5 years after randomization. The primary end point was progression of liver disease, as indicated by death, hepatocellular carcinoma, hepatic decompensation, or, for those with bridging fibrosis at baseline, an increase in the Ishak fibrosis score of 2 or more points. Results: We randomly assigned the patients to receive peginterferon (517 patients) or no therapy (533 patients) for 3.5 years. The level of serum aminotransferases, the level of serum hepatitis C virus RNA, and histologic necroinflammatory scores all decreased significantly (P<0.001) with treatment, but there was no significant difference between the groups in the rate of any primary outcome (34.1% in the treatment group and 33.8% in the control group; hazard ratio, 1.01; 95% confidence interval, 0.81 to 1.27; P=0.90). The percentage of patients with at least one serious adverse event was 38.6% in the treatment group and 31.8% in the control group (P=0.07). Conclusions: Long-term therapy with peginterferon did not reduce the rate of disease progression in patients with chronic hepatitis C and advanced fibrosis, with or without cirrhosis, who had not had a response to initial treatment with peginterferon and ribavirin. (ClinicalTrials.gov number, NCT00006164.).
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页码:2429 / 2441
页数:13
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