JAC Advance Access published online on November 25, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkh015
© 2003 by The British Society for Antimicrobial Chemotherapy
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Leading article
1 Department of Internal Medicine IV, Gastroenterology and
Hepatology, University of Vienna,
Waehringer Guertel 18-20, A 1090 Vienna, Austria
* Corresponding author. E-mail: peter.ferenci{at}akh-wien.ac.at.
A substantial proportion of patients infected with
hepatitis C virus (HCV) genotype 1 still does not respond to pegylated
interferon-alfa/ribavirin (IFN/RBV) therapy.
Factors which identify potential non-responders are needed to limit
exposure to drugs in patients unlikely to benefit from treatment
and to save health care resources. Host predictive factors have
a low negative predictive value. In contrast, viral factors have
a high precision in predicting outcome of therapy. Viral kinetics
are the basis for the study of response of therapy. The decrease
in viral load within 24 h after administration of a single test
dose of conventional IFN reflects the IFN-sensitivity of the virus
strain and predicts the outcome of conventional IFN/RBV therapy
even before treatment with a specificity of 100% and a
sensitivity of 83%. In contrast to conventional IFN, the
two available PEG-IFN preparations differ considerably in how they
suppress viral replication, and cut-off values have to be prospectively
established separately for each drug. Patients without an early
virological response (HCV-RNA either undetectable or decrease by
Keywords: HCV, therapy, outcome prediction
Predicting the therapeutic response in patients
with chronic
hepatitis C: the role of viral kinetic studies
2 log10 after 12 weeks)
(EVR), do not achieve a sustained virological response (SVR; negative
predictive value: 97-98%). Thus, in the absence
of an EVR, treatment should be stopped. The outcome of PEG-IFN alfa-2a/RBV
combination therapy is dependent on the rapidity of the virological
response. Patients who become HCV-RNA negative after 4 weeks have
the best chance of achieving an SVR. The rapidity of viral elimination
may be a useful guide to tailoring the length of treatment in patients with
an EVR.![]()
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