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JAC Advance Access published online on January 5, 2006

Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dki458
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© The Author 2005. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Received April 27, 2005
Revised October 10, 2005
Accepted November 20, 2005

Brief report

Dose-dependent and genotype-independent sustained virological response of a 12 week pegylated interferon alpha-2b treatment for acute hepatitis C

Francesco G. De Rosa 1 *, Olivia Bargiacchi 1, Sabrina Audagnotto 1, Silvia Garazzino 1, Giuseppe Cariti 1, Riccardo Raiteri 1, and Giovanni Di Perri 1

1 Department of Infectious Diseases, University of Turin, Turin, Italy

* To whom correspondence should be addressed.
Francesco G. De Rosa, E-mail: francescogiuseppe.derosa{at}unito.it


   Abstract

Objectives: The optimal regimen for acute hepatitis C (AHC) is considered to be a 24 week treatment with interferon (IFN) alpha-2b. A 24 week treatment with pegylated IFN (PEG-IFN) alpha-2b is also effective. This study was designed to assess response rates to a 12 week regimen of PEG-IFN alpha-2b.

Patients and methods: Patients with AHC were treated with PEG-IFN alpha-2b for 12 weeks in an open, non-randomized, prospective cohort study. Diagnosis of AHC was made with positive serum HCV RNA and elevated alanine aminotransferase (ALT) levels with a documented seroconversion or a known risk factor in the preceding 6 months. Treatment was administered within a median of 31 days (range 0-116) of the ALT level peak at a dosage varying from 1.06 to 1.66 µg/kg/week. The primary end-point was a sustained virological response (SVR).

Results: Nineteen patients were treated, of whom 11 patients (57.9%) had HCV genotype 1. Fourteen patients were asymptomatic. An SVR was achieved in 74% of patients and the SVR rate was 100 and 83.3%, respectively, in genotype 1 and non-1 infected patients treated with a dosage ≥1.33 µg/kg, compared with 40 and 50%, respectively, in those who received a lower dosage. An SVR was significantly associated by multivariate analysis only with PEG-IFN dosage ≥1.33 µg/kg/week. No significant association was found with any viral genotype.

Conclusions: The rate of SVR was independent of the HCV genotype and was significantly associated by multivariate analysis only with the higher PEG-IFN dosage. Early identification and treatment of AHC is likely to decrease the burden of chronic hepatitis, especially when caused by HCV genotype 1.

Keywords: hepatitis C virus; acute hepatitis; interferon treatment; IFN; HCV.
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J Antimicrob ChemotherHome page
J. Wiegand, K. Deterding, M. Cornberg, and H. Wedemeyer
Treatment of acute hepatitis C: the success of monotherapy with (pegylated) interferon {alpha}
J. Antimicrob. Chemother., November 1, 2008; 62(5): 860 - 865.
[Abstract] [Full Text] [PDF]



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