Table 2.
Characteristic | SVR, n = 34 (41.5 %) | R/NR, n = 48 (58.5 %) | p-Value |
---|---|---|---|
Age at the end of treatment (years) | |||
Median (range) | 15.5 (4–17) | 14 (5–17) | 0.420 |
<12 | 5 (14.7 %) | 9 (18.8 %) | 0.632 |
Gender | |||
Girls | 15 (44.1 %) | 19 (39.6 %) | 0.681 |
Boys | 19 (55.9 %) | 29 (60.4 %) | |
Liver fibrosis (F) stage (Scheuer) | |||
Available | 32 | 46 | |
F0–F1 | 17 (53.1 %) | 28 (60.9 %) | 0.529 |
F2–F4 | 15 (46.9 %) | 18 (39.1 %) | |
Liver activity (A) grade (Scheuer) | |||
Available | 32 | 46 | |
A0–A1 | 16 (50.0 %) | 19 (41.3 %) | 0.626 |
A2–A4 | 16 (50.0 %) | 27 (58.7 %) | |
Baseline ALT (U/l) | |||
Median (range) | 33.5 (10–191) | 42.5 (19–285) | 0.087 |
Abnormal | 18 (52.9 %) | 30 (62.5 %) | |
Baseline GGTP (U/l) | |||
Median (range) | 22 (6–94) | 27.5 (6–122) | 0.158 |
Abnormal | 4 (11.8 %) | 10 (20.8 %) | |
HCV genotype | |||
1 | 22 (64.7 %) | 27 (56.3 %) | 0.442 |
4 | 12 (35.3 %) | 21 (43.7 %) | |
Baseline viral load (IU/ml) | |||
Median (range), ×105 | 4.3 (0.037–30.2) | 3.5 (0.25–54.5) | 0.290 |
≥600,000 | 14 (41.2 %) | 18 (37.5 %) | 0.737 |
≥800,000 | 5 (14.7 %) | 14 (29.2 %) | 0.126 |
After 12 weeks of treatment | |||
EVR | 34 (100.0 %) | 22 (45.8 %) | –a |
cEVR | 20 (58.8 %) | 5 (10.4 %) | –a |
aNot tested due to discontinuation of treatment in patients who did not achieve EVR