Table 4.
CRS7 Risk Group and Risks of Outcomes
All patients – Multivariate§§ | Caucasians only - Multivariate§§ | ||||||
---|---|---|---|---|---|---|---|
CRS7 Risk Group | N | OR/HR (95% CI) | p-value | N | OR/HR (95% CI) | p-value | |
Fibrosis Progression* | High | 226 | 1.61 (1.00–2.59) | 0.05 | 158 | 1.60 (0.95–2.70) | 0.08 |
Int | 161 | 1.28 (0.76–2.15) | 0.35 | 114 | 1.30 (0.74–2.30) | 0.36 | |
Low | 106 | - | - | 90 | - | - | |
Trend | 493 | 1.27 (1.01–1.58) | 0.04 | 362 | 1.26 (0.98–1.62) | 0.07 | |
CRS7a Continuous | 493 | 1.13 (1.04–1.22) | 0.003 | 362 | 1.14 (1.04–1.25) | 0.004 | |
| |||||||
Cirrhosis§ | High | 440 | 1.39 (0.98–1.99) | 0.07 | 302 | 1.39 (0.93–2.07) | 0.11 |
Int | 310 | 1.13 (0.77–1.64) | 0.53 | 211 | 1.00 (0.66–1.53) | 1.00 | |
Low | 188 | - | - | 164 | - | - | |
Trend | 938 | 1.19 (1.00–1.41) | 0.05 | 677 | 1.19 (0.98–1.45) | 0.08 | |
CRS7a Continuous | 938 | 1.07 (0.99–1.15) | 0.07 | 677 | 1.08 (0.99–1.17) | 0.08 | |
| |||||||
Clinical outcome‡ | High | 440 | 1.36 (0.95–1.95) | 0.09 | 302 | 1.34 (0.89–2.02) | 0.16 |
Int | 310 | 1.30 (0.89–1.90) | 0.17 | 211 | 1.47 (0.97–2.25) | 0.07 | |
Low | 188 | - | - | 164 | - | - | |
Trend | 938 | 1.14 (0.97–1.35) | 0.12 | 677 | 1.12 (0.93–1.36) | 0.23 | |
CRS7a Continuous | 938 | 1.05 (0.98–1.13) | 0.15 | 677 | 1.05 (0.97–1.14) | 0.21 | |
| |||||||
HCC‡ | High | 440 | 1.65 (0.84–3.24) | 0.15 | 302 | 1.88 (0.88–4.01) | 0.10 |
Int | 309 | 1.09 (0.52–2.28) | 0.83 | 210 | 0.89 (0.36–2.17) | 0.79 | |
Low | 188 | - | - | 164 | - | - | |
Trend | 937 | 1.34 (0.97–1.85) | 0.07 | 676 | 1.48 (1.00–2.18) | 0.05 | |
CRS7a Continuous | 937 | 1.09 (0.96–1.25) | 0.19 | 676 | 1.14 (0.97–1.33) | 0.11 |
Complementary Log-Log Model (HR).
Logistic Regression Model (OR),
Cox Proportional Hazards Model (HR).
Fibrosis Progression, cirrhosis and clinical outcome multivariate models were adjusted for race, patient type, clinical site and treatment assignment.
OR/HR for 0.1-unit change in continuous CRS7
Multivariate HCC models were adjusted for race, treatment assignment, patient type, clinical site and cirrhosis at baseline.
All p-values are derived from two-sided tests.