Table 2. Rates of SVR for patients with compensated cirrhosis HCV genotype 2–4 (phase III/IV studies).
HCV Genotype | Regimen | Duration | Patients | SVR rate | Study (reference) |
---|---|---|---|---|---|
HCV genotype 3 | DCV – SOF | 12 weeks | Naïve and TE | 58–97% | ALLY-3 43 |
HCV genotype 2
HCV genotype 3 |
SOF + RBV
|
12 weeks
12 weeks |
Naïve
|
91%
34% |
FISSION
40
|
HCV genotype 2
HCV genotype 3 |
SOF + RBV
|
12 weeks
12 weeks |
Naïve
|
94%
21% |
POSITRON
39
|
HCV genotype 3
HCV genotype 2 HCV genotype 3 |
SOF + RBV
|
24 weeks
12 weeks 24 weeks |
Naïve
TE TE |
92%
78% 62% |
VALENCE
92
|
HCV genotype 2
HCV genotype 3 HCV genotype 3 |
SOF + RBV
|
16 weeks
24 weeks 16 weeks 24 weeks 16 weeks 24 weeks |
TE
Naïve TE |
87%
100% 57% 82% 47% 76% |
BOSON STUDY
44
|
HCV genotype 2
|
SOF + RBV
|
12 weeks
|
Naïve
TE |
67%
76% |
Trio Network
85
|
HCV genotype 2
HCV genotype 3 |
SOF + RBV
SOF + RBV |
12 weeks
16 weeks 12 weeks 16 weeks |
TE
TE |
60%
78% 19% 61% |
FUSION
39
|
HCV genotype non-1 | SOF – VPV | 12 weeks | Naïve and TE | 100% | ASTRAL-1 45 |
HCV genotype 2 | SOF – VPV | 12 weeks | Naïve and TE | 100% | ASTRAL-2 93 |
HCV genotype 3 | SOF – VPV | 12 weeks | Naïve and TE | 91% | ASTRAL-3 93 |
HCV genotype 3
|
DCV – SOF + RBV
|
12 weeks
16 weeks |
Naïve and TE
|
83%
89% |
ALLY-3+
94
|
a. Abbreviations: DCV, daclatasvir; HCV, hepatitis C virus; RBV, ribavirin; SOF, sofosbuvir; SVR, sustained virological response; TE, treatment-experienced; VPV, velpatasvir