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Prognostic value of Ishak fibrosis stage: Findings from the hepatitis C antiviral long-term treatment against cirrhosis trial

dc.contributor.authorEverhart, James E.en_US
dc.contributor.authorWright, Elizabeth C.en_US
dc.contributor.authorGoodman, Zachary D.en_US
dc.contributor.authorDienstag, Jules L.en_US
dc.contributor.authorHoefs, John C.en_US
dc.contributor.authorKleiner, David E.en_US
dc.contributor.authorGhany, Marc G.en_US
dc.contributor.authorMills, A. Scotten_US
dc.contributor.authorNash, S. Russellen_US
dc.contributor.authorGovindarajan, Suganthaen_US
dc.contributor.authorRogers, Thomas E.en_US
dc.contributor.authorGreenson, Joel K.en_US
dc.contributor.authorBrunt, Elizabeth M.en_US
dc.contributor.authorBonkovsky, Herbert L.en_US
dc.contributor.authorMorishima, Chihiroen_US
dc.contributor.authorLitman, Heather J.en_US
dc.date.accessioned2010-02-02T15:32:32Z
dc.date.available2011-03-01T16:26:45Zen_US
dc.date.issued2010-02en_US
dc.identifier.citationEverhart, James E.; Wright, Elizabeth C.; Goodman, Zachary D.; Dienstag, Jules L.; Hoefs, John C.; Kleiner, David E.; Ghany, Marc G.; Mills, A. Scott; Nash, S. Russell; Govindarajan, Sugantha; Rogers, Thomas E.; Greenson, Joel K.; Brunt, Elizabeth M.; Bonkovsky, Herbert L.; Morishima, Chihiro; Litman, Heather J. (2010). "Prognostic value of Ishak fibrosis stage: Findings from the hepatitis C antiviral long-term treatment against cirrhosis trial." Hepatology 51(2): 585-594. <http://hdl.handle.net/2027.42/64929>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/64929
dc.description.abstractStudies 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 fragmentation 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. (H EPATOLOGY 2010;51:585–594.)en_US
dc.format.extent485973 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titlePrognostic value of Ishak fibrosis stage: Findings from the hepatitis C antiviral long-term treatment against cirrhosis trialen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Health System, Ann Arbor, MIen_US
dc.contributor.affiliationotherDivision of Digestive Diseases and Nutrition, National Institutes of Health, Department of Health and Human Services, Bethesda, MD ; fax: 301-480-8300. ; Epidemiology and Clinical Trials Branch, Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, 2 Democracy Plaza, Room 655, 6707 Democracy Boulevard, MSC 5450, Bethesda, MD 20892-5450en_US
dc.contributor.affiliationotherOffice of the Director, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MDen_US
dc.contributor.affiliationotherArmed Forces Institute of Pathology, Division of Hepatic Pathology and Veterans Administration Special Reference Laboratory for Pathology, Washington, DCen_US
dc.contributor.affiliationotherGastrointestinal Unit (Medical Services), Massachusetts General Hospital and the Department of Medicine, Harvard Medical School, Boston, MAen_US
dc.contributor.affiliationotherDivision of Gastroenterology, University of California–Irvine, Irvine, CAen_US
dc.contributor.affiliationotherLaboratory of Pathology, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MDen_US
dc.contributor.affiliationotherLiver Diseases Branch, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Department of Health and Human Services, Bethesda, MDen_US
dc.contributor.affiliationotherDepartment of Pathology, Virginia Commonwealth University Medical Center, Richmond, VAen_US
dc.contributor.affiliationotherColorado GI Pathology, Centennial, COen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Southern California at Rancho Los Amigos Medical Center, Downey, CAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TXen_US
dc.contributor.affiliationotherDepartment of Pathology and Immunology, Washington University, St. Louis, MOen_US
dc.contributor.affiliationotherDepartments of Medicine and Molecular and Structural Biology and The Liver-Biliary-Pancreatic Center, University of Connecticut Health Center, Farmington, CTen_US
dc.contributor.affiliationotherVirology Division, Department of Laboratory Medicine, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherNew England Research Institutes, Watertown, MAen_US
dc.identifier.pmid20101752en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/64929/1/23315_ftp.pdf
dc.identifier.doi10.1002/hep.23315en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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