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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: J Hepatol. 2016 Feb 22;64(6):1232–1239. doi: 10.1016/j.jhep.2016.02.022

Table 1.

Patients’ characteristics

Patients Characteristics Cohort (n=58) SOF+SIM (n=19) SOF+DAC (n=19) SOF+LEDI (n=20) P
Mean Age ± SD (yr) 60±11 60±11 60±13 61±10 0.8685
Mean Weight ± SD (kg) 71±16 72±17 67±14 74±13 0.4787
Male – N (%) 30 (52%) 10 (53%) 8 (42%) 12 (60%) 0.5329
HCV Load – Mean ± SD (Log10 IU/ml) 6.05±0.85 5.70±1.05 6.45±0.45 5.99±0.46 0.0065
HCV Genotype – N (%) 0.2736
1 50 (86%) 15 (79%) 16 (85%) 19 (95%)
3 1 (2%) 0 1 (5%) 0
4 6 (10%) 4 (21%) 1 (5%) 1 (5%)
5 1 (2%) 0 1 (5%) 0
HIV Coinfected – N (%) 5 (9%) 3 (16%) 1 (5%) 1 (5%) 0.3977
Severe Fibrosis (F3) – N(%) 25 (43%) 12 (63%) 6 (32%) 7 (35%) 0.0963
Cirrhosis (F4) – N (%) 33 (57%) 7 (37%) 13 (68%) 13 (65%) 0.0963
Treatment History 0.6720
 Treatment naive 14(24%) 5 (26%) 5 (26%) 4 (20%)
 Previously Treated – N(%) 44 (76%) 14 (74%) 14 (74%) 16 (80%)
 Previous Regimen – N 0.0182
PegIFN-RBV 29 (66%) of 44 13 (93%) of 14 8 (57%) of 14 8 (50%) of 16
PegIFN-RBV + Telaprevir 8 (19%) of 44 0 1 (7%) of 14 7 (44%) of 16
PegIFN-RBV + Boceprevir 1 (2%) of 44 0 0 1 (6%) of 16
Protease Inhibitor 4 (9%) of 44 1 (7%) of 14 3 (21%) of 14 0
PegIFN alone 1 (2%) of 44 0 1 (7%) of 14 0
Sofosbuvir + RBV 1 (2%) of 44 0 1 (7%) of 14 0
Previous Response** - N 0.0138
Non-Responders 33 (75%) of 44 12 (86%) of 14 13 (93%) of 14 8 (50%) of 16
Relapsers 11 (25%) of 44 2 (14%) of 14 1 (7%) of 14 8 (50%) of 16
*

Kruskal-Wallis test for continuous data, and χ2 test for categorical data; SOF, sofosbuvir; DAC, daclatasvir; SIM, simeprevir; LEDI, ledipasvir; SD, one standard deviation; Fibrosis, F, stage (see Methods); Non-responders, detected HCV RNA throughout treatment; Relapsers, HCV RNA not detected at the end of therapy but detectable during follow-up;

**

more information in Table S2.