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Published Online First: 15 March 2007. doi:10.1136/gut.2006.106690
Gut 2007;56:1111-1116
Copyright © 2007 BMJ Publishing Group Ltd & British Society of Gastroenterology.

LIVER

Rapid and early virological response to chronic hepatitis C treatment with IFN {alpha}2b or PEG-IFN {alpha}2b plus ribavirin in HIV/HCV co-infected patients

Christopher Payan1, Adeline Pivert2, Patrice Morand3, Samira Fafi-Kremer3, Fabrice Carrat4, Stanislas Pol5, Patrice Cacoub6, Christian Perronne7, Françoise Lunel2 and the ANRS HC02 RIBAVIC study team

1 Département de Microbiologie-EA3882, CHU-Hôpital Morvan, Brest, France
2 Laboratoire de Bactériologie-Virologie-Hygiène Hospitalière, CHU Angers, France
3 Laboratoire de Virologie, CHU Grenoble, France
4 INSERM U707, Faculté de Médecine St Antoine, Paris, France
5 Service d’Hépatologie, Hôpital Cochin, INSERM U567, Université René Descartes, Paris, France
6 Service de Médecine Interne, Hôpital Pitié-Salpétrière, Paris, France
7 Service des Maladies Infectieuses et Tropicales, Hôpital Raymond Poincaré, Paris, France

Correspondence to:
Correspondence to:
Professor Françoise Lunel
Laboratoire de Bactériologie-Virologie-Hygiène Hospitalière, CHU Angers, 4 rue Larrey, 49933 Angers Cedex, France; frlunel-fabiani{at}chu-angers.fr

Background and aims: An algorithm based on a 2 log10 decline in hepatitis C virus (HCV) RNA at week (W) 12 has been proposed in US and European recommendations for the management of patients with chronic hepatitis C treated with pegylated-interferon and ribavirin.

Methods: We examined rapid virological response (RVR; at W2 and W4 after the initiation of therapy) in HIV/HCV co-infected patients. Using HCV RNA measurements (Versant HCV RNA 3.0, Cobas Amplicor HCV 2.0), RVR was studied in 323 patients from the ANRS HC02 RIBAVIC trial, comparing interferon {alpha}2b 3 MU x3/week with pegylated interferon {alpha}2b 1.5 µg/kg/week, each combined with ribavirin 800 mg/day over 48 weeks.

Results: The best positive and negative predictive values of sustained virological response (SVR) were obtained with an undetectable HCV RNA at W4 (97%) and with more than a 2 log10 decrease at W12 (99%), respectively. Prediction of non-SVR was obtained in all patients by using HCV RNA cut-off levels above 460 000 IU/ml at W4 and above 39 000 UI/ml at W12 irrespective of the HCV genotype and arm of treatment.

Conclusion: We propose a new algorithm based on RVR thresholds using HCV RNA that allows for excellent prediction of non-SVR as early as W4.

Abbreviations: EVR, early virological response; HAART, highly active antiretroviral treatment; HCV, hepatitis C virus; IFN, interferon; NPV, negative predictive value; NR, non-responders; PEG-IFN, pegylated interferon; PPV, positive predictive value; RB, responders with breakthrough; ROC, receiver operating characteristics; RR, responders with relapse; RVR, rapid virological response; SVR, sustained virological response/responders

Keywords: HIV/HCV co-infection; hepatitis C therapy; HCV viral load; rapid and early viral decline; prediction of response


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This article has been cited by other articles:

  • Poordad, F., Landaverde, C. (2009). Review: Rapid virological response to peginterferon alfa and ribavirin treatment of chronic hepatitis C predicts sustained virological response and relapse in genotype 1 patients. Therapeutic Advances in Gastroenterology 2: 91-97 [Abstract]  

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