Abstract
Background: The current standard-of-care for treatment of HCV genotype 2 (GT-2) patients is the combination of sofosbuvir (SOF) with weight-based ribavirin (RBV). Patients with HCV GT-2 infection and ribavirin contraindications require the use of SOF plus NS5A inhibitor daclatasvir (DCV) which is not reimbursed everywhere. Methods: We conducted an open-label observational, prospective study on a subgroup of GT-2 patients either naïve or treatment experienced (TE) with contraindications to the use of RBV. Patients with cirrhosis of Child–Pugh–Turcotte (CPT) class A and B or advanced fibrosis with comorbidities were included. They were assigned to receive 12 or 24 weeks of SOF/DCV. The primary end point of the study was sustained virological response (SVR) defined as HCV RNA levels
Original language | English |
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Pages (from-to) | 971-976 |
Number of pages | 6 |
Journal | Liver International |
Volume | 36 |
Issue number | 7 |
DOIs | |
Publication status | Published - Jul 1 2016 |
Keywords
- daclatasvir
- genotype-2
- ribavirin free
- sofosbuvir
ASJC Scopus subject areas
- Hepatology