In the initial treatment of chronic hepatitis C, interferon-alfa (IFN-alpha
) monotherapy for 24-48 weeks induces sustained response rates of only 10-2
0%. Combination therapy with IFN-alpha plus ribavirin induces a sustained r
esponse in 40-50% of patients, and can be now recommended as the firstline
therapy for chronic hepatitis C. Stopping therapy at week 12 because of per
sistent viraemia is unnecessary with the combination therapy because later
clearance of HCV RNA can still occur with a sustained response. Patients wi
th HCV genotype 1 should receive 48 weeks of combination therapy, in contra
st to 24 weeks for patients with genotypes 2 or 3. For patients who cannot
tolerate the side effects of ribavirin, such as anaemia, IFN-alpha at 3 MU
three times weekly for 48 weeks is preferred as the initial therapy. The lo
ng-acting pegylated IFN can be expected to enhance the efficacy of combinat
ion therapy in the treatment of chronic hepatitis C and appears to be much
more potent as monotherapy. Further studies are needed to improve the curre
nt 'half-full' status of chronic hepatitis C treatment. (C) 2000 Blackwell
Science Asia Pty Ltd.