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. 2016 Jan;12(1):23–30.

Table 1.

Major Trials Evaluating Direct-Acting Antiviral Agents in the Treatment of Post-Liver Transplant HCV Recurrence

Study Genotype, n (%) Severity of liver disease, n (%) Treatment Duration SVR12 by Genotype, n (%) SVR12 by Severity, n (%)
Charlton23,a 1a: 22 (55)
1b: 11 (28)
3: 6 (15)
4: 1 (3)
F0: 1 (3)
F1-2: 14 (35)
F3: 9 (23)
F4: 16 (40)
Sofosbuvir + ribavirin 24 weeks 1a: 16 (73)
1b: 6 (55)
3: 6 (100)
F0: 1 (100)
F1-2: 10 (71)
F3: 7 (78)
F4: 10 (63)
Forns24,a 1a: 36 (35)
1b: 49 (47)
2: 1 (1)
3: 7 (7)
4: 7 (7)
Multiple: 4 (4)
All patients had either aggressive recurrent disease or cirrhosis Sofosbuvir + ribavirin 24-48
weeks
N/A Early recurrence: 35 (73)
Cirrhosis: 19 (43)
Charlton26,b 1a: 164 (72)
1b: 63 (28)
4: 2 (1)
No cirrhosis: 111 (48)
CTP A: 51 (22)
CTP B: 52 (23)
CTP C: 9 (4)
FCH: 6 (3)
Sofosbuvir + ledipasvir + ribavirin 12 weeks N/A No cirrhosis: 53 (96)
CTP A: 25 (96)
CTP B: 22 (85)
CTP C: 3 (60)
FCH: 4 (100)
24 weeks N/A No cirrhosis: 55 (98)
CTP A: 24 (96)
CTP B: 23 (88)
CTP C: 3 (75)
FCH: 2 (100)
Saab27,a 1: all patients F0: 13 (46)
F1: 2 (7)
F2: 2 (8)
F3: 6 (23)
F4: 5 (19)
Sofosbuvir + simeprevir 12 weeks N/A Overall SVR12: 28 (93)
Pungpapong28,a 1a: 74 (60)
1b: 43 (35)
Unclear: 6 (5)
F0-2: 85 (70)
F3-4: 37 (30)
Sofosbuvir + simeprevir ± ribavirin 12 weeks 1a: 64 (86)
1b: 41 (95)
F0-2: 67 (81)
F3-4: 34 (93)
Gutierrez29,a 1a: 35 (57)
1b: 26 (43)
F0-2: 38 (62)
F3-4: 23 (38)
Sofosbuvir + simeprevir ± ribavirin 12 weeks 1a: 31 (89)
1b: 26 (100)
F0-2: 38 (100)
F3-4: 19 (83)
Kwo34,b 1a: 29 (85)
1b: 5 (15)
F0: 6 (18)
F1: 13 (38)
F2: 15 (44)
Ombitasvir + paritaprevir with ritonavir + dasabuvir 24 weeks 1a: 28 (97)
1b: 5 (100)
N/A
Poordad33,c 1a: 31 (58)
1b: 10 (19)
3: 11 (21)
6: 1 (2)
F0-2: 23 (43)
F3: 13 (25)
F4: 16 (30)
Not reported: 1 (2)
Sofosbuvir + daclatasvir + ribavirin 12 weeks 1a: 30 (97)
1b: 9 (90)
3: 10 (91)
6: 1 (100)
N/A

CTP, Child-Turcotte-Pugh; FCH, fibrosing cholestatic hepatitis; HCV, hepatitis C virus; SVR, sustained virologic response.

a

Real-life cohort.

b

Phase 2 trial.

c

Phase 3 trial.