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. 2020 May 5;15(5):e0232773. doi: 10.1371/journal.pone.0232773

Table 2. Baseline characteristics and treatment results in patients receiving an IFN-free DAA regimen.

IFN-free regimens Complete cohort GZR/EBR GLE/PIB OBV/PTV/r OBV/PTV/r SOF±RBV SOF+DCV SOF/LDV SOF+SIM SOF/VEL/ SOF/VEL
No of therapies n = 878 (%) n = 30 (%) n = 47 (%) n = 21 (%) +DSV, n = 84 (%) n = 49 (%) n = 34 (%) n = 449 (%) n = 26 (%) VOX, n = 14 (%) n = 124 (%)
Age (y, mean ± SD) 53.1 ± 12.9 56.6 ± 14.4 50.0 ± 11.0 48.7 ± 13.7 59.2 ± 12.5 55.9 ± 11.2 55.3 ± 8.7 52.1 ± 13.2 57.1 ± 10.6 59.4 ± 11.3 50.1 ± 12.3
Sex (male/female) 486 (55) / 392 (45) 23 (77) / 7 (23) 26 (55) / 21 (45) 14 (66)/ 7 (33) 42 (50) / 42 (50) 28 (57) / 21 (43) 23 (68) / 11 (32) 237 (53) / 212 (47) 18 (69) / 8 (31) 11 (79) / 3 (21) 80 (65) / 44 (35)
Transplanted patients 54 (6) 1 (3) 0 (0) 0 (0) 0 (0) 14 (29) 5 (15) 22 (5) 9 (35) 1 (7) 2 (2)
People with HIV 38 (4) 1 (3) 0 (0) 0 (0) 1 (1) 4 (8) 5 (15) 15 (3) 0 (0) 0 (0) 12 (10)
Liver cirrhosis 254 (29) 12 (40) 1 (2) 2 (10) 23 (27) 13 (27) 22 (65) 117 (26) 18 (69) 8 (57) 38 (31)
 Child-Pugh score A/B/C 180/71/3 9/3/0 1/0/0 2/0/0 21/2/0 8/5/0 12/9/1 87/29/1 9/9/0 3/5/0 28/9/1
IFN-experienced 267 (30) 1 (3) 5 (11) 4 (19) 21 (25) 28 (57) 18 (53) 147 (33) 14 (54) 6 (43) 23 (19)
HCV Genotype
 1 (a/b/c/unclassified) 616 [70] (270/327/3/16) 28 [93] (6/22/0/0) 25 [53] (16/8/0/1) 0 (0) 82 [98] (6/76/0/0) 7 [14] (2/5/0/0) 17 [50] (7/9/0/1) 414 [92] (209/190/2/13) 20 [77] (7/11/1/1) 9 [64] (6/3/0/0) 14 [11] (11/3/0/0)
 2 44 (5) 0 (0) 6 (13) 0 (0) 0 (0) 25 (51) 0 (0) 0 (0) 0 (0) 2 (14) 11 (9)
 3 148 (17) 0 (0) 10 (21) 0 (0) 0 (0) 12 (24) 15 (44) 14 (3) 2 (8) 2 (14) 93 (75)
 4 58 (7) 2 (7) 4 (9) 21 (100) 1 (1) 3 (6) 2 (6) 17 (4) 4 (15) 1 (7) 3 (2)
 5 2 (0) 0 (0) 1 (2) 0 (0) 0 (0) 1 (2) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0)
 6 3 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 3 (1) 0 (0) 0 (0) 0 (0)
 1/3 coinfection 2 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 1 (0) 0 (0) 0 (0) 1 (1)
 2k/1b 2 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 2 (2)
 Unknown 3 (0) 0 (0) 1 (2) 0 (0) 1 (1) 1 (2) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0)
Outcome parameters
Lost to follow-up 78 (9) 6 (20) 1 (2) 4 (19) 5 (6) 2 (4) 1 (3) 48 (11) 1 (4) 0 (0) 10 (8)
Documented 12-wk FU after EoT 800 (91) 24 (80) 46 (98) 17 (81) 79 (94) 47 (96) 33 (97) 401 (89) 25 (96) 14 (100) 114 (92)
Virological relapse 48 (6) 1 (4) 0 (0) 0 (0) 2 (3) 8 (17) 6 (18) 23 (6) 5 (20) 1 (7) 2 (2)
SVR 752 (94) 23 (96) 46 (100) 17 (100) 77 (97) 39 (83) 27 (82) 378 (94) 20 (80) 13 (93) 112 (98)
 GT 1a 212/231 (92) 3/4 (75) 16/16 (100) n/a 4/5 (80) 2/2 (100) 3/6 (50) 168/178 (94) 4/6 (67) 5/6 (83) 7/8 (88)
 GT 1b 295/306 (96) 18/18 (100) 8/8 (100) n/a 71/72 (99) 3/5 (60) 9/9 (100) 171/177 (97) 9/11 (82) 3/3 (100) 3/3 (100)
 GT 2 35/40 (88) n/a 5/5 (100) n/a n/a 19/24 (79) n/a n/a n/a 2/2 (100) 9/9 (100)
 GT 3 136/142 (96) n/a 10/10 (100) n/a n/a 10/11 (91) 12/15 (80) 12/14 (86) 2/2 (100) 2/2 (100) 88/89 (99)
 GT 4 48/51 (94) 2/2 (100) 4/4 (100) 17/17 (100) 1/1 (100) 3/3 (100) 2/2 (100) 12/15 (80) 4/4 (100) 1/1 (100) 2/2 (100)
 GT 5 2/2 (100) n/a 1/1 (100) n/a n/a 1/1 (100) n/a n/a n/a n/a n/a
 GT 6 2/3 (67) n/a n/a n/a n/a n/a n/a 2/3 (67) n/a n/a n/a

SVR rates were calculated taking all patients with a documented 12-week FU after EoT into account. Values shown are percentages and counts and mean values with the corresponding standard deviation.

Abbreviations: DAA, direct-acting antiviral; DCV, daclatasvir; DSV, dasabuvir; EBR, elbasvir; EoT, end of treatment; FU, follow-up; GLE, glecaprevir; GZR, grazoprevir; HCV, hepatitis C virus; HIV, human immunodeficiency virus; IFN, interferon; LDV, ledipasvir; n/a, not applicable; OBV, ombitasvir; PIB, pibrentasvir; PTV, paritaprevir; r, ritonavir; RBV, ribavirin; SD, standard deviation; SIM, simeprevir; SOF, sofosbuvir; SVR, sustained virological response; VEL, velpatasvir; VOX, voxilaprevir.