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. 2017 Feb 24;142:83–122. doi: 10.1016/j.antiviral.2017.02.014

Table 6.

Efficacy of 400 mg sofosbuvir QD + ribavirin for 12 weeks.

Cirrhosis Prior treatment SVR12 rate
Study and trial phase Ref.
GT-1 GT-2 GT-3 GT-4
No cirrhosis
Naïve 84% (21/25) 100% (4/4) 100% (6/6) Electron, phase 2a Gane et al., 2013a
Null response 10% (1/10)
Naïve 90.9% (10/11) Phase 2 Ruane et al., 2015
Experienced 61.5% (8/13)
Experienced 92.4% (85/92) 67.9% (57/84) POSITRON, phase 3 Jacobson et al., 2013
Experienced 96.2% (25/26) 36.8% (14/38) FUSION, phase 3
Naïve 98.3% (58/59) 61.4% (89/145) FISSION, phase 3 Lawitz et al., 2013a
Naïve 91.9% (159/173) 75% (42/56) HCV-TARGET, phase 4 Feld et al., 2016a, Welzel et al., 2016a
Experienced 87.5% (42/48) 84.6% (22/26)
Naïve 97.6% (80/82) Phase 3 Omata et al., 2014
Experienced 96.3% (52/54)
Naïve 96.7% (29/30) 0% (0/2) VALENCE, phase 3 Zeuzem et al., 2014a
Experienced 93.8% (30/32) 42.9% (3/7)
Naïve 86.4% (19/22) Egyptian study Doss et al., 2015
Experienced 72.7% (16/22)
Naïve or experienced 86.4% (19/22) Real-world study Maasoumy et al., 2016

Cirrhosis Naïve 33.3% (1/3) Phase 2 Ruane et al., 2015
Experienced 50% (2/4)
Naïve 100% (2/2) VALENCE, phase 3 Zeuzem et al., 2014a
Experienced 77.8% (7/9) 0% (0/2)
Naïve 76.6% (36/47) VALOR, phase 4 Ho et al., 2017
Experienced 84.2% (16/19)
Experienced 94.1% (16/17) 21.4% (3/14) POSITRON, phase 3 Jacobson et al., 2013
Experienced 60% (6/10) 19.2% (5/26) FUSION, phase 3
Naïve 71.9% (23/32) 55.3% (21/38) HCV-TARGET, phase 4 Feld et al., 2016a, Welzel et al., 2016a
Experienced 86.7% (26/30) 37.9% (22/58)
Naïve 90.9% (10/11) 34.2% (13/38) FISSION, phase 3 Lawitz et al., 2013a
Naïve 100% (8/8) Phase 3 Omata et al., 2014
Experienced 88.9% (8/9)
Naïve 66.7% (2/3) Egyptian study Doss et al., 2015
Experienced 60% (3/5)
Naïve or experienced 90% (9/10) Real-world study Maasoumy et al., 2016
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