Literature DB >> 14762857

Sustained viral response to interferon and ribavirin in liver transplant recipients with recurrent hepatitis C.

Manal F Abdelmalek1, Roberto J Firpi, Consuelo Soldevila-Pico, Alan I Reed, Alan W Hemming, Chen Liu, James M Crawford, Gary L Davis, David R Nelson.   

Abstract

Recurrent hepatitis C infection is an important cause of progressive fibrosis, cirrhosis, and graft loss following orthotopic liver transplantation. Treatment for posttransplant recurrence of hepatitis C with interferon-based therapy is difficult but results in loss of detectable virus in up to 30% of patients. However, the durability of viral clearance and the associated histologic response in this setting is unknown. The aim of this study was to determine whether viral loss in response to antiviral therapy is durable and associated with improvement in liver histology. All liver transplant recipients who received interferon-based treatment for recurrent hepatitis C virus (HCV) at the University of Florida from 1991 to 2002 were included in this study. Patients who lost detectable HCV after treatment with interferon alone or in combination with ribavirin were followed to assess the durability of viral response and its impact on liver histology. One hundred nineteen transplant recipients were treated with interferon or combination therapy. Twenty-nine (20 men, 9 women; mean age, 54 yrs [range, 42-74 yrs]) lost detectable HCV RNA and remained virus negative for at least 6 months after discontinuing therapy (sustained viral response[SVR]). The mean follow-up after discontinuing therapy was 24.7 months (range, 6-70 mos). Our study cohort included one patient with SVR following interferon monotherapy and 28 patients with SVR following combination therapy with interferon plus ribavirin. All patients remained HCV RNA negative (assessed by polymerase chain reaction or branched-DNA assay) during follow-up of up to 5 years. Liver histology assessed 2 years after treatment showed less inflammation compared with before treatment in 50% and showed no change in 38%. By 3 to 5 years post-treatment (n = 15 recipients), inflammation was reduced in 60% and remained unchanged in 33%. Fibrosis stage at 2 years improved by > or = 1 stage in 27 %, remained unchanged in 38 %, and worsened in 35% despite viral clearance. At 3 to 5 years, the fibrosis stage had improved in 67%, remained unchanged in 13%, and worsened in 20%. Both grade of inflammation and fibrosis stage improved by 3 to 5 years posttreatment compared with baseline histology (p < 0.05). In conclusion, loss of HCV after treatment of recurrent chronic hepatitis C with interferon and ribavirin is durable, and the durability of the SVR is associated with improvement in hepatic inflammation and regression of fibrosis.

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Year:  2004        PMID: 14762857     DOI: 10.1002/lt.20074

Source DB:  PubMed          Journal:  Liver Transpl        ISSN: 1527-6465            Impact factor:   5.799


  15 in total

1.  A pharmacokinetic/viral kinetic model to evaluate treatment of chronic HCV infection with a non-nucleoside polymerase inhibitor.

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Journal:  Antivir Ther       Date:  2018

Review 2.  Living donor liver transplantation to patients with hepatitis C virus cirrhosis.

Authors:  Yasuhiko Sugawara; Masatoshi Makuuchi
Journal:  World J Gastroenterol       Date:  2006-07-28       Impact factor: 5.742

3.  Hepatic decompensation/serious adverse events in post-liver transplantation recipients on sofosbuvir for recurrent hepatitis C virus.

Authors:  Neal Patel; Kian Bichoupan; Lawrence Ku; Rachana Yalamanchili; Alyson Harty; Donald Gardenier; Michel Ng; David Motamed; Viktoriya Khaitova; Nancy Bach; Charissa Chang; Priya Grewal; Meena Bansal; Ritu Agarwal; Lawrence Liu; Gene Im; Jennifer Leong; Leona Kim-Schluger; Joseph Odin; Jawad Ahmad; Scott Friedman; Douglas Dieterich; Thomas Schiano; Ponni Perumalswami; Andrea Branch
Journal:  World J Gastroenterol       Date:  2016-03-07       Impact factor: 5.742

Review 4.  Natural history, treatment and prevention of hepatitis C recurrence after liver transplantation: past, present and future.

Authors:  Jérôme Dumortier; Olivier Boillot; Jean-Yves Scoazec
Journal:  World J Gastroenterol       Date:  2014-08-28       Impact factor: 5.742

5.  Long-term leukocyte natural α-interferon and ribavirin treatment in hepatitis C virus recurrence after liver transplantation.

Authors:  Mariarosa Tamè; Federica Buonfiglioli; Massimo Del Gaudio; Andrea Lisotti; Paolo Cecinato; Antonio Colecchia; Francesco Azzaroli; Antonietta D'Errico; Rosario Arena; Claudio Calvanese; Chiara Quarneti; Giorgio Ballardini; Antonio Daniele Pinna; Giuseppe Mazzella
Journal:  World J Gastroenterol       Date:  2013-08-28       Impact factor: 5.742

6.  Clearance of hepatitis C virus after living-donor liver transplantation in spite of residual viremia on end date of interferon therapy before transplantation.

Authors:  Tatsuki Ichikawa; Kazuhiko Nakao; Keisuke Hamasaki; Takuya Honda; Hidetaka Shibata; Mana Akahoshi; Susumu Eguchi; Mitsuhisa Takatsuki; Takashi Kanematsu; Katsumi Eguchi
Journal:  World J Gastroenterol       Date:  2007-08-14       Impact factor: 5.742

Review 7.  Hepatitis C viral kinetics: the past, present, and future.

Authors:  Anushree Chatterjee; Patrick F Smith; Alan S Perelson
Journal:  Clin Liver Dis       Date:  2013-02       Impact factor: 6.126

Review 8.  Management of hepatitis C infection after liver transplantation.

Authors:  Mazen Alsatie; Naga Chalasani; Paul Y Kwo
Journal:  Drugs       Date:  2007       Impact factor: 9.546

Review 9.  Challenges of recurrent hepatitis C in the liver transplant patient.

Authors:  Renumathy Dhanasekaran; Roberto J Firpi
Journal:  World J Gastroenterol       Date:  2014-04-07       Impact factor: 5.742

10.  Persistence of hepatitis C RNA in liver allografts is associated with histologic progression independent of serologic viral clearance.

Authors:  M Ghabril; R C Dickson; M Krishna; R Lloyd; J Aranda-Michel; A Keaveny; R Satyanarayana; H Bonatti
Journal:  J Transplant       Date:  2009-05-05
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