Published online Nov 6, 2015. doi: 10.4292/wjgpt.v6.i4.114
Peer-review started: May 21, 2015
First decision: July 10, 2015
Revised: July 15, 2015
Accepted: September 10, 2015
Article in press: September 16, 2015
Published online: November 6, 2015
Processing time: 175 Days and 21.1 Hours
Recently, direct antiviral agents (DAAs) have been increasingly used for the treatment of chronic hepatitis C virus (HCV) infections, replacing interferon-based regimens that have severe adverse effects and low tolerability. The constant supply of new DAAs makes shorter treatment periods with enhanced safety possible. The efficacy of DAAs for treatment of compensated liver cirrhosis (LC) is not less than that for treatment of non-cirrhotic conditions. These clinical advantages have been useful in pre- and post-liver transplantation (LT) settings. Moreover, DAAs can be used to treat decompensated HCV-induced LC in elderly patients or those with severe complications otherwise having poor prognosis. Although encouraging clinical data are beginning to appear, the actual efficacy of DAAs for suppressing disease progression, allowing delisting for LT and, most importantly, improving prognosis of patients with decompensated HCV-LC remains unknown. Case-control studies to examine the short- or long-term effects of DAAs for treatment of decompensated HCV-LC are urgently need.
Core tip: Decompensated liver cirrhosis (LC) due to hepatitis C virus (HCV) infection is a severe disease with poor prognosis. Because interferon-included regimens are contraindicated at this stage, liver transplantation has been the only way to cure the disease. However, recent development of direct antiviral agents (DAAs) is offering a hope for this difficult situation. Promising antiviral effects of DAAs for LC have been observed, suggesting they might be useful for treatment of decompensated HCV-LC. To explore this possibility, large case-control studies are needed.