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Histologic outcomes in hepatitis C–infected patients with varying degrees of virologic response to interferon-based treatments

dc.contributor.authorPockros, Paul J.en_US
dc.contributor.authorHamzeh, Fayez M.en_US
dc.contributor.authorMartin, Paulen_US
dc.contributor.authorLentz, Ellenen_US
dc.contributor.authorZhou, Xiaoleien_US
dc.contributor.authorGovindarajan, Suganthaen_US
dc.contributor.authorLok, Anna Suk-Fongen_US
dc.date.accessioned2010-10-06T14:57:13Z
dc.date.available2011-03-01T16:26:44Zen_US
dc.date.issued2010-10en_US
dc.identifier.citationPockros, Paul J.; Hamzeh, Fayez M.; Martin, Paul; Lentz, Ellen; Zhou, Xiaolei; Govindarajan, Sugantha; Lok, Anna S. (2010). "Histologic outcomes in hepatitis C–infected patients with varying degrees of virologic response to interferon-based treatments." Hepatology 52(4): 1193-1200. <http://hdl.handle.net/2027.42/78076>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/78076
dc.description.abstractPatients with chronic hepatitis C with partial virologic response or nonresponse to interferon-based therapies can experience treatment-related improvements in liver histology. This retrospective analysis assessed the histologic response to treatment in patients with varying degrees of virologic response (sustained virologic response [SVR], breakthrough, relapse, or nonresponse), time to hepatitis C virus (HCV) RNA undetectability, and duration of viral suppression. Patients (HCV genotypes 1-6) with baseline and follow-up liver biopsies from eight phase 2 to phase 4 interferon-based trials were analyzed. Blinded biopsies were evaluated by a single pathologist. Improvements or worsening of METAVIR necroinflammatory activity and fibrosis were defined as increase or decrease of ≥1 grading category from baseline to 24 weeks after end of treatment. A majority of the 1571 patients with paired biopsy data were white, male, with HCV genotype 1/4, baseline HCV RNA levels >800,000 IU/mL, and baseline alanine aminotransferase levels ≤3 × upper limit of the normal range; mean baseline activity and fibrosis scores were 1.8 and 1.7, respectively. Overall, 80% of patients received peginterferon alfa-2a monotherapy or peginterferon alfa-2a/ribavirin combination therapy. Mean treatment duration was 46 weeks. There was a positive correlation between the degree of virologic response and improvements in METAVIR activity and fibrosis, and an inverse correlation with worsening activity and fibrosis (all comparisons, P < 0.0001). Patients with SVR had the greatest histologic benefit. As a combined group, relapsers and patients with breakthrough had significantly greater benefits than nonresponders (activity, P = 0.0001; fibrosis, P = 0.003). Consistent with these results, a better histologic response was correlated with a shorter time to undetectable HCV RNA and a longer duration of viral suppression (all comparisons, P < 0.0001). Conclusion: In patients with chronic hepatitis C who were treated with interferon-based therapies, histologic benefits may be observed even in the absence of an SVR. (H EPATOLOGY 2010;)en_US
dc.format.extent171877 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.titleHistologic outcomes in hepatitis C–infected patients with varying degrees of virologic response to interferon-based treatmentsen_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.affiliationumUniversity of Michigan Medical Center, Ann Arbor, MIen_US
dc.contributor.affiliationotherScripps Clinic, La Jolla, CA ; fax: 858-554-8065 ; Division of Gastroenterology/Hepatology, Scripps Clinic, 10666, North Torrey Pines Road, La Jolla, CA 92037en_US
dc.contributor.affiliationotherGenentech, Inc., South San Francisco, CAen_US
dc.contributor.affiliationotherMiller School of Medicine, University of Miami, Miami, FLen_US
dc.contributor.affiliationotherGenentech, Inc., South San Francisco, CAen_US
dc.contributor.affiliationotherRTI Health Solutions, Research Triangle Park, NCen_US
dc.contributor.affiliationotherUniversity of Southern California–Keck School of Medicine and Liver Research Laboratory, Downey, CAen_US
dc.identifier.pmid20658462en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78076/1/23809_ftp.pdf
dc.identifier.doi10.1002/hep.23809en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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