Table 4.
Genotype | Cirrhosis status | Prior treatment | Grazoprevir–elbasvir | Glecaprevir–pibrentasvir | Sofosbuvir–velpatasvir | Sofosbuvir–velpatasvir–voxilaprevir |
---|---|---|---|---|---|---|
1b | No cirrhosis | Naive | 12 weeks | 8 weeks | 12 weeks | No |
Peg-IFN + RBV | ||||||
Compensated cirrhosis | Naive | |||||
Peg-IFN + RBV | 12 weeks | |||||
1a, 2, 4, 5, 6 | No cirrhosis | Naive | Noa | 8 weeks | 12 weeks | No |
Peg-IFN + RBV | ||||||
Compensated cirrhosis | Naive | |||||
Peg-IFN + RBV | 12 weeks | |||||
3 | No cirrhosis | Naive | No | 8 weeks | 12 weeks | No |
Peg-IFN + RBV | 12–16 weeks | No | ||||
Compensated cirrhosis | Naive | 8 weeks | 12 weeksb | 12 weeks | ||
Peg-IFN + RBV | 16 weeks | 12 weeks |
Data from ref.5. DAA, direct-acting antiviral agent; EASL, European Association for the Study of the Liver; Peg-IFN, pegylated interferon-α. a12 weeks of treatment possible in patients infected with hepatitis C virus (HCV) genotype 1 without nonstructural protein 5A (NS5A) resistance-associated substitutions (RASs). bIn patients with the Y93H RAS, either addition of ribavirin (RBV) or an alternative regimen is recommended. EASL recommends this approach only in those with cirrhosis.