Abstract :
Chronic infections with the hepatitis C virus
(HCV) represent a major global health
problem, with around 170 million patients at risk
of developing life-threatening complications such
as liver cirrhosis or hepatocellular carcinoma. The
standard treatment of care is a combination of
weekly pegylated interferon (peginterferon) alfa and
daily ribavirin for 24-72 weeks, dependent on HCV
genotype and the patient’s individual virological
response to therapy (1, 2). Currently, there are two
forms of peginterferon licensed for the treatment of
hepatitis C: peginterferon alfa-2a (Pegasys, Roche) and
peginterferon alfa-2b (Pegintron, Schering-Plough).
Although direct pharmacodynamic comparisons
of both substances have shown that they differ
considerably with respect to pharmocokinetics and
initial virological suppression (3), it remained largely
unclear whether this is relevant for clinical endpoints,
especially for achieving sustained virological response
in HCV-infected patients.
Keywords :
HCV , C virus , Meta-Analysis , IDEAL