Abstract
The
development of potent antivirals able to directly block multiple step of
viral lifecycle (DAAs) led to a revolution in HCV treatment. These
compounds are associated with unprecedent high rates of SVR and can be
administered orally, regardless of the severity of the associated liver
disease, allowing treatment of large number of HCV infected patients.
Three main classes of DAAs are currently available, NS3/4 inhibitors,
NS5A inhibitors and NS5B inhibitors. They can be combined according to 2
different strategies, the use of a backbone drug with high barrier of
resistance as the NS5B inhibitor sofosbuvir, with the addition of a
second drug either NS3/4 or NS5A, or the use of more than 1 drug from
different classes to simultaneously attack the virus at different
sequence sites. DAAs can be administered for 12 or 24 weeks in the
majority of patients, although attempts to reduce to 6-8 weeks the
treatment duration in patients with baseline favorable characteristics
are ongoing. Overall, SVR rates ensured by the currently approved
combinations, are 90% or higher. Although cirrhotic patients and in
particular patients with decompensated disease may represent a difficult
to cure group, data from real life confirm evidence derived from phase
III studies showing improvement in biochemical parameters, even in such a
special populations. We can expect, the number of patients with unmeet
medical needs will decline over time in the next 4 years. This review
aim to discuss updated regimens by HCV genotype and to provide a brief
summary of the coming strategies.
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