Studies address length of treatment for hepatitis C
BSIP, Cavallini James/Science Photo Library
 Hepatitis C relapse rates affected by treatment duration |
Data from studies addressing treatment duration for hepatitis C infection were presented at the annual meeting of the European
Association for the Study of the Liver held in Vienna last week.
One study, involving 1,469 patients with chronic hepatitis C (HCV) genotypes
2 and 3, showed that 24 weeks of peginterferon alfa-2a (180µg once
weekly) combined with ribavirin (800mg daily) achieves higher cure rates
than 16 weeks of treatment. Sustained virological response was observed
in 76 per cent of those who received 24 weeks of treatment compared with
65 per cent of those who received the shorter treatment.
Lead investigator Mitchell Shiffman of Virginia Commonwealth University
medical centre, Richmond, Virginia, commented: “Although three
small studies have suggested that treating these patients for a shorter
duration may be effective and some physicians have already adopted this
approach, this large study has clearly demonstrated that patients with
HCV genotypes 2 and 3, including those with a rapid virological response,
really do need 24 weeks of treatment.”
The study was supported by Roche.
A second study, examining treatment outcome for peginterferon alfa-2b
(1.5µg/kg weekly) with ribavirin (800mg daily or a weight-based
dose up to 1,400mg daily) in 1,829 patients with HCV genotypes 2 and
3, showed that 24 weeks of therapy was as effective as 48 weeks.
The shorter 24-week regimen was associated with a relapse rate of 5 per
cent in genotype 2 patients and 10 per cent in genotype 3 patients compared
with 5 per cent and 12 per cent, respectively, in the longer 48-week
regimen. In the 24-week arm, patients with genotype 2 also had a higher
sustained virological response than those with genotype 3 (72 per cent
versus 59 per cent). The investigators conclude that higher, weight-based
doses of ribavirin appear to be necessary to achieve similar response
rates in genotype 3 patients.
The study was supported by Schering-Plough. |