“…Pegylated IFNs appear to increase the risk of non-respiratory infections independently from neutropenia [17], which may be explained by their distinctive pharmacokinetic differences from standard IFN [23]. A sustained virological response was achieved in three (33.3%) patients, which is similar to previous series with IFN-based therapies in patients with cirrhosis, where HCV eradication rates were between 10% and 30%, especially in HCV genotype non-1 patients (up to 50%) [6,7,15,19,[24][25][26]. However, in view of the low response rates (20%) to antiviral therapy in patients with recurrent disease after liver transplantation or with preemptive antiviral therapy in patients undergoing liver transplantation [21,27], a pre-transplant approach seems to be reasonable.…”