Copyright
©The Author(s) 2018.
World J Hepatol. Feb 27, 2018; 10(2): 267-276
Published online Feb 27, 2018. doi: 10.4254/wjh.v10.i2.267
Published online Feb 27, 2018. doi: 10.4254/wjh.v10.i2.267
Ref. | Treatment N /sample size | Country | Male gender n (%) | Age (yr) | Genotype n (%) | Duration of follow up | Cirrhosis n (%) | History of HCC n (%) | HCC occurrence | HCC recurrence |
Ioannou et al[33] | IFN only = 35871 (58%), DAA + IFN = 4535 (7.2%), DAA only = 21948 (35%) n = 62354 | United States | 96.60% | Mean 55.8 ± 7.6 | G1 = 77.4 %, G2 = 13.5%, G3 = 8.3%, G4 = 0 | Mean follow-up DAA only group = 1.53 years, DAA+IFN group= 3.6 yr, IFN only group = 9.1 yr | Cirrhosis: 16.8%, decompe-nsated cirrhosis: 4.7% | None | Total 3271 incident cases. IFN group = 0.81/100 person years, DAA + IFN = 1.06 /100 py, DAA only = 1.32/100 py | Not applicable |
Kanwal et al[34] | All DAA treated n = 22500 | United States | 21761 (96.7%) | Mean 61.6 ± 6.1 | G1 = 19531 (86.8%), G2 = 1422 (6.3%), G3 = 940 (4.2%), G 4-6 = 217 (1%) | 22963 person years of follow-up | 8766 (39.0%) | None | 271 (1.2) | Not applicable |
ANRS CO22 HEP ATH-ER et al[35] | DAA group = 189, no DAA = 78 n =267 | France | DAA group = 147 (78%) | DAA group = 62 ± 9 yr, no DAAs = 66 ± 10 yr | 65 % genotype 1 | Median: 20.2 mo after DAA initiation and 26.1 mo for untreated patients | Cirrhosis: DAA group = 152 (80%), no DAAs = 55 (72 %) | All treated | Not Applicable | DAA group = 24 (12.7%), no DAAs = 16 (20.5%) |
ANRS CO12 CIRVIR et al[35] | DAA group = 13, no DAA = 66 n = 79 | France | DAA group = 11 (85%), no DAA = 39 (59%) | DAA group = 61 ± 10 yr, no DAA = 65 ± 9 yr | Genotype 1: DAA group = 11 (85%), no DAA group = 53/63 (84 %) | All cirrhotic | All treated | Not Applicable | DAA group = 1 (7.7%), no DAAs = 31 (47%) | |
ANRS CO23 CUPILT et al[35] | All DAA treated n = 314 | France | 257 (82%) | 61 ± 8 yr | 212 (67.5%) genotype 1 | 49 (15.6%) | Treated | Not Applicable | 7 (2.2%) | |
Cabibbo et al[36] | All DAA treated n = 143 | Italy | 80 (60.1) | Mean 70.4 ± 8.9 | G1a: 9 (6.3), 1b: 114 (79.7), G2: 9 (6.3), G3: 7 (4.9), G4: 4 (2.8) | 6, 12 and 18 mo | All cirrhotic | All treated | Not applicable | 6-, 12- and 18-mo HCC recurrence rates were 12%, 26.6% and 29.1%, respectively |
Nagata et al[37] | IFN-based: 1145. IFN-free DAA group: 752 n = 1897 | Tokyo | IFN group: 621 (54), IFN free: 340 (45) | Median: IFN group: 59 (19-79); IFN free: 69 (24-87) | IFN group: G1a = 8 (7), G1b = 833 (73), G2a = 182 (16), G2b = 105 (9), G3 = 1 (0) | Median for IFN group: 6.8 (0.2-22.0); IFN free: 1.8 (0.1–7.7) | 5% of IFN group, 11% of IFN free group | IFN group: 18 (2.5%). IFN-free group: 7 (1.1%) | IFN group: 18 (53%). IFN-free group: 22 (29%) | |
Ikeda et al[38] | All DAA treated n = 177 | Japan | M:F = 52: 37 in each group | DAA group: 71 (39-85) | Median 20.7 mo | All treated | Not applicable | HCC recurrence rates at 1st and 2nd year were 18.1 and 25.0% in pts with DAA therapy and 21.8 and 46.5% in those without DAAs, (P = 0.003) | ||
Zanetto et al[39] | DAA treated= 23, control = 23 n = 46 | Italy | DAA group = 59 (49-69), controls= 58 (46 -70) | DAA group: G1a = 5 (22), Gb = 9 (39), G2 = 1 (4), G3 = 5 (22), G4 = 3 (13) | Median= DAA group = 10 mo, Control group = 7 mo | All cirrhotic | All treated | Not applicable | 12.5% of DAA-treated patients and 8.3% of control group had HCC recurrence (P = 0.60) | |
Zavaglia et al[40] | All DAA treated n = 31 | Italy | 20 (64.5) | Mean 65 ± 8 | G1a = 4 (13), G1b = 23(74), G2 = 2 (6.5), G4 = 2 (6.5) | Median 8 mo | All cirrhotic | All treated | Not applicable | 1 (3.2) |
Ogata et al[41] | All DAA treated n = 1170 | Japan | 493 (42) | Median = 67 (21-88) | All genotype 1 | Time from the end of DAA therapy until last visit: 1.3 yr | None | 22 cases (1.8%) | Not applicable | |
Minami et al[42] | DAA group = 27, IFN group = 38, Controls = 861 n = 926 | Japan | DAA group: 18 (67), IFN group: 27 (71), Controls: 489 (57) | Median age: DAA group = 71 (48-82) IFN group = 66 (49-79), Control = 71 (44–91) | Genotype 1: DAA = 21 (78), IFN = 29 (76), Controls = 633 (74). Genotype 2: DAA= 6 (22), IFN= 9 (24), Control= 147 (17) | 1 and 2 yr | All treated | Not applicable | Cumulative recurrence rates at 1 and 2 yr were 21.1% and 29.8%, respectively, in the DAA group, 26.3% and 52.9%, respectively, in the IFN group, and 30.5% and 61.0%, respectively, in the control group | |
Deterding et al[43] | n = 974 | Germany | G1 = 743 (76.2) | All had advanced cirrhosis | 12 (1.2) | |||||
Degasperi et al[44] | n = 565 | Italy | 60% | Median age = 65 (30-87) yr | G1a = 15%, G1b = 49%, G2 = 13%, G3 = 11%, G4 = 12%, G5 = 1% | Median 42 wk for occu-rrence, 39 wk for recurrence | All cirrhotic | 48 (8%) | 20 (4%) estimated annual incidence of 1.6% | 9 (19%), annual incidence of 7 .7% |
Bourliere et al[45] | DAA + RBV ± PEG IFN = 21%. IFN free DAA therapy = 79% n = 1393 | 47 (19-79) yr | 2.5 (0.6-4.3) yr | 0 (0) | 0 (0) | |||||
Nagaoki et al[46] | PEG-IFN/ RBV = 244, DCV/ASV = 154 n = 398 | Japan | All genotype 1 | Median for PEG-IFN/RBV = 96 (10–196) and DCV/ASV group = 23 (4–78) mo | PEG-IFN/RBV = 13 (5.3%), DCV/ASV group = 7 (4.5%) | |||||
Cheung et al[47] | All DAA | United Kingdom | 198 (48.8) 171 (42.1) | 15 mo | All decompensated cirrhosis | 29 (71.4%) | 17 (5%) | 2 | ||
Mettke et al[48] | 158 DAA treated, 184 controls | Germany | Median = 440 (91–908) and 592 (90-1000) d | All cirrhotic | 6 and 14 patients during follow-up, resulting in an HCC incidence of 2.9 (AVT) and 4.48 (Con) per 100 py, respectively | |||||
Ji et al[49] | China | 51% | Mean age 51 | 82.2% genotype 1b | Median 14 (3-35) mo | 48% cirrhotic | None | Not applicable | ||
Innes et al[50] | Scotland | 1.8 yr | None | 44 (5.1%) | Not applicable | |||||
Torres et al[51] | All DAA treated | United States | 7 (87.5%) | Median 64 (57-87) years | G1 = 6 (75%), mixed genotype = 2 (25%) | 12 mo | 7 (87.5%) | All treated | Not applicable | 0 (0) |
- Citation: Butt AS, Sharif F, Abid S. Impact of direct acting antivirals on occurrence and recurrence of hepatocellular carcinoma: Biologically plausible or an epiphenomenon? World J Hepatol 2018; 10(2): 267-276
- URL: https://www.wjgnet.com/1948-5182/full/v10/i2/267.htm
- DOI: https://dx.doi.org/10.4254/wjh.v10.i2.267