Prognostic Value of Ishak Fibrosis Stage: Findings from the Hepatitis C Antiviral Long-Term Treatment Against Cirrhosis Trial

被引:127
作者
Everhart, James E. [1 ]
Wright, Elizabeth C. [2 ]
Goodman, Zachary D. [3 ,4 ]
Dienstag, Jules L. [5 ,6 ]
Hoefs, John C. [7 ]
Kleiner, David E. [8 ]
Ghany, Marc G. [9 ]
Mills, A. Scott [10 ]
Nash, S. Russell [11 ]
Govindarajan, Sugantha [12 ]
Rogers, Thomas E. [13 ]
Greenson, Joel K. [14 ]
Brunt, Elizabeth M. [15 ]
Bonkovsky, Herbert L. [16 ,17 ,18 ]
Morishima, Chihiro [19 ]
Litman, Heather J. [20 ]
机构
[1] NIDDK, Epidemiol & Clin Trials Branch, Div Digest Dis & Nutr, NIH,Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[2] NIDDK, Off Director, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[3] Armed Forces Inst Pathol, Div Hepat Pathol, Washington, DC 20306 USA
[4] Vet Adm, Special Reference Lab Pathol, Washington, DC USA
[5] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Gastrointestinal Unit,Med Serv, Boston, MA USA
[6] Harvard Univ, Dept Med, Sch Med, Boston, MA USA
[7] Univ Calif Irvine, Div Gastroenterol, Irvine, CA USA
[8] NCI, Pathol Lab, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[9] NIDDK, Liver Dis Branch, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[10] Virginia Commonwealth Univ, Med Ctr, Dept Pathol, Richmond, VA USA
[11] Colorado GI Pathol, Centennial, CO USA
[12] Univ So Calif, Dept Pathol, Rancho Los Amigos Med Ctr, Doumey, CA USA
[13] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[14] Univ Michigan Hlth Syst, Dept Pathol, Ann Arbor, MI USA
[15] Washington Univ, Dept Pathol & Immunol, St Louis, MO USA
[16] Univ Connecticut, Ctr Hlth, Dept Med, Farmington, CT USA
[17] Univ Connecticut, Ctr Hlth, Dept Mol & Struct Biol, Farmington, CT USA
[18] Univ Connecticut, Ctr Hlth, Liver Biliary Pancreat Ctr, Farmington, CT USA
[19] Univ Washington, Dept Lab Med, Div Virol, Seattle, WA 98195 USA
[20] New England Res Inst, Watertown, MA 02172 USA
基金
美国国家卫生研究院;
关键词
PERCUTANEOUS LIVER-BIOPSY; NATURAL-HISTORY; PROGRESSION; CLASSIFICATION; REVERSAL; THERAPY;
D O I
10.1002/hep.23315
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Studies of the prognostic value of Ishak fibrosis stage are lacking. We used multi-year follow-up of the Hepatitis C Antiviral Long-Term Treatment Against Cirrhosis (HALT-C) Trial to determine whether individual Ishak fibrosis stages predicted clinical outcomes in patients with chronic hepatitis C. Baseline liver biopsy specimens from 1050 patients with compensated chronic hepatitis C who had failed combination peginterferon and ribavirin were reviewed by a panel of expert hepatopathologists. Fibrosis was staged with the Ishak scale (ranging from 0 = no fibrosis to 6 = cirrhosis). Biopsy fiagmentation and length as well as number of portal tracts were recorded. We compared rates of prespecified clinical outcomes of hepatic decompensation and hepatocellular carcinoma across individual Ishak fibrosis stages. Of 1050 biopsy specimens, 25% were fragmented, 63% longer than 1.5 cm) 69% larger than 10 mm(2), and 75% had 10 or more portal tracts. Baseline laboratory markers of liver disease severity were worse and the frequency of esophageal varices higher with increasing Ishak stage (P < 0.0001). The 6-year cumulative incidence of first clinical outcome was 5.6% for stage 2, 16.1% for stage 3, 19.3% for stage 4, 37.8% for stage 5, and 49.3% for stage 6. Among nonfragmented biopsy specimens, the predictive ability of Ishak staging was enhanced; however, no association was observed between Ishak stage and outcomes for fragmented biopsy specimens because of high rates of outcomes for patients with noncirrhotic stages. Similar results were observed with liver transplantation or liver-related death as the outcome. Conclusion: Ishak fibrosis stage predicts clinical outcomes, need for liver transplantation, and liver-related death in patients with chronic hepatitis C. Patients with fragmented biopsy specimens with low Ishak stage may be understaged histologically. (HEPATOLOGY 2010;51:585-594.)
引用
收藏
页码:585 / 594
页数:10
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