Antiviral therapy is generally indicated in patients who have histologic ev
idence of chronic hepatitis and ongoing viral replication. The aim of treat
ment is to normalize alanine aminotransferase levels and to eliminate virus
replication. Interferon-alfa (IFN-alpha) is the most used agent. The stand
ard treatment regimen for hepatitis B e antigen (HBeAg)-positive cirrhosis
is based on IFN-alpha given alone, but the efficacy of new antivirals (famc
iclovir, lamivudine) with or without IFN-alpha is currently under investiga
tion. Conversely, the therapy of antiHBe-positive cirrhosis is far from bei
ng satisfactory. The results of treatment of patients affected by type C ci
rrhosis with IFN-alpha alone have been disappointing, as 10-15% of treated
patients shows a sustained virologic response. Although current evidence su
ggests that the combination of ribavirin and IFN-alpha might be more effica
cious than IFN alone in increasing the response rare in patients in the adv
anced fibrotic stage, the efficacy of this regimen for patients with well-c
ompensated HCV-related cirrhosis is still unknown and prospective well desi
gned studies are urgently needed. Patients with decompensated cirrhosis are
not generally treated unless they are included in liver transplantation pr
ograms. Prospective long-term trials with large sample sizes are needed to
determine if responders to IFN-alpha have a low incidence of liver-related
complications and hepatocellular carcinoma.