Table 2.
Comparison of factors influencing the SVR rate in treated patients
| Variable | Relapsers (n = 75) | Non-responders (n = 42) | |
|---|---|---|---|
| Gender | |||
| Male (n = 91) | 61/63 (97) | 27/28 (96) | |
| Female (n = 26) | 12/12 (100) | 14/14 (100) | |
| p-value | < 0.09 | < 0.06 | |
| Age (years), n (%) | |||
| 30-50 | 48/49 (98) | 27/27 (100) | |
| 51-65 | 25/26 (96) | 14/15 (93) | |
| p-value | < 0.06 | < 0.05 | |
| Baseline HCV RNA (log10 IU/l), n (%) | |||
| ≤ 100,000 IU/ml | 49/51 (96) | 19/19 (100) | |
| ≥ 100,000 IU/ml | 24/24 (100) | 22/23 (96) | |
| p-value | < 0.08 | < 0.07 | |
| Fibrosis stages | |||
| F1-F2 | 28/28 (100) | 9/9 (100) | |
| F3-F4 | 45/47 (96) | 32/33 (97) | |
| p-value | < 0.07 | < 0.06 | |
| Undetectable HCV PCR, n (%) | |||
| 4 weeks | 61/75 (81) | 30/42 (71) | |
| 24 weeks | 12/75 (16) | 11/42 (26) | |
| p-value | < 0.005 | < 0.002 | |
| RBV dose, n (%) | |||
| No dose modification | 54/54 (100) | 31/31 (100) | |
| Reduction in RBV dose | 12/12 (100) | 6/6 (100) | |
| Stop RBV | 7/9 (78) | 4/5 (80) | |
| p-value | < 0.003 | < 0.005 | |
SVR – sustained virological response, RVR – rapid virological response, RBV – ribavirin