Factors Predictive of HBsAg Loss for the 360 Propensity Score-Matched Patients
Variable | Comparison | Univariate Analysis | Multivariate Analysis | ||
HR (95% CI) | P value | HR (95% CI) | P value | ||
Start entecavir treatment | |||||
Age | Increase per y | 1.03 (0.98–1.08) | .22 | ||
Sex | Male vs female | 0.77 (0.30–1.98) | .59 | ||
ALT | Increase per U/L | 1.000 (0.999–1.001) | .82 | ||
ALT, U/L | <2×, 2-5 ×, and >5 × ULN | 0.94 (0.55–1.63) | .83 | ||
Total bilirubin | Increase per mg/dL | 1.01 (0.81–1.26) | .93 | ||
Prior interferon use | Yes vs no | 0.28 (0.04–2.08) | .21 | ||
HBV DNA at baseline | Increase per 1 unit | 0.68 (0.50–0.92) | .012 | ||
HBV genotype, C vs B | C vs B | 0.90 (0.30–2.69) | .85 | ||
Platelet | Increase per 103/μL | 1.000 (0.992–1.009) | .92 | ||
FIB-4 index | Increase per 1 unit | 1.01 (0.90–1.14) | .83 | ||
HBsAg at baseline | Increase per log10 IU/mL | 0.26 (0.15–0.46) | <.001 | ||
HBsAg at 12 mo of treatment | Increase per log10 IU/mL | 0.18 (0.09–0.36) | <.001 | ||
Groups | Discontinued vs continued | 4.53 (1.52–13.56) | .007 | 5.27 (1.72–16.14) | .004 |
End of treatment (discontinued group) or 3 y of treatment (continued group) | |||||
Age, per y | Increase per y | 1.03 (0.99–1.08) | .19 | ||
ALT, U/L | Increase per U/L | 0.97 (0.92–1.01) | .14 | ||
Total bilirubin, mg/dL | Increase per mg/dL | 0.38 (0.07–1.92) | .24 | ||
FIB-4 index, per 1 unit | Increase per 1 unit | 1.17 (0.72–1.92) | .53 | ||
HBsAg, per log10 IU/mL | Increase per log10 IU/mL | 0.12 (0.06–0.23) | <.001 | 0.11 (0.05–0.21) | <.001 |
HBsAg, <150 vs ≥150 IU/mL | Yes vs no | 14.04 (5.06–38.97) | <.001 | ||
HBsAg decline from baseline | Increase per log10 IU/mL | 1.32 (0.66–2.46) | .47 | ||
Consolidation duration, per wk | Increase per wk | 1.012 (1.001–1.022) | .025 | ||
≥78 vs <78 wk | 0.84 (0.11–6.56) | .87 | |||
≥104 vs <104 wk | 0.81 (0.23–2.87) | .75 | |||
≥130 vs <130 wk | 0.82 (0.33–2.04) | .66 |
Variable | Comparison | Univariate Analysis | Multivariate Analysis | ||
HR (95% CI) | P value | HR (95% CI) | P value | ||
Start entecavir treatment | |||||
Age | Increase per y | 1.03 (0.98–1.08) | .22 | ||
Sex | Male vs female | 0.77 (0.30–1.98) | .59 | ||
ALT | Increase per U/L | 1.000 (0.999–1.001) | .82 | ||
ALT, U/L | <2×, 2-5 ×, and >5 × ULN | 0.94 (0.55–1.63) | .83 | ||
Total bilirubin | Increase per mg/dL | 1.01 (0.81–1.26) | .93 | ||
Prior interferon use | Yes vs no | 0.28 (0.04–2.08) | .21 | ||
HBV DNA at baseline | Increase per 1 unit | 0.68 (0.50–0.92) | .012 | ||
HBV genotype, C vs B | C vs B | 0.90 (0.30–2.69) | .85 | ||
Platelet | Increase per 103/μL | 1.000 (0.992–1.009) | .92 | ||
FIB-4 index | Increase per 1 unit | 1.01 (0.90–1.14) | .83 | ||
HBsAg at baseline | Increase per log10 IU/mL | 0.26 (0.15–0.46) | <.001 | ||
HBsAg at 12 mo of treatment | Increase per log10 IU/mL | 0.18 (0.09–0.36) | <.001 | ||
Groups | Discontinued vs continued | 4.53 (1.52–13.56) | .007 | 5.27 (1.72–16.14) | .004 |
End of treatment (discontinued group) or 3 y of treatment (continued group) | |||||
Age, per y | Increase per y | 1.03 (0.99–1.08) | .19 | ||
ALT, U/L | Increase per U/L | 0.97 (0.92–1.01) | .14 | ||
Total bilirubin, mg/dL | Increase per mg/dL | 0.38 (0.07–1.92) | .24 | ||
FIB-4 index, per 1 unit | Increase per 1 unit | 1.17 (0.72–1.92) | .53 | ||
HBsAg, per log10 IU/mL | Increase per log10 IU/mL | 0.12 (0.06–0.23) | <.001 | 0.11 (0.05–0.21) | <.001 |
HBsAg, <150 vs ≥150 IU/mL | Yes vs no | 14.04 (5.06–38.97) | <.001 | ||
HBsAg decline from baseline | Increase per log10 IU/mL | 1.32 (0.66–2.46) | .47 | ||
Consolidation duration, per wk | Increase per wk | 1.012 (1.001–1.022) | .025 | ||
≥78 vs <78 wk | 0.84 (0.11–6.56) | .87 | |||
≥104 vs <104 wk | 0.81 (0.23–2.87) | .75 | |||
≥130 vs <130 wk | 0.82 (0.33–2.04) | .66 |
Abbreviations: ALT, alanine aminotransferase, CI, confidence interval; FIB-4, fibrosis 4; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; HR, hazard ratio.
Factors Predictive of HBsAg Loss for the 360 Propensity Score-Matched Patients
Variable | Comparison | Univariate Analysis | Multivariate Analysis | ||
HR (95% CI) | P value | HR (95% CI) | P value | ||
Start entecavir treatment | |||||
Age | Increase per y | 1.03 (0.98–1.08) | .22 | ||
Sex | Male vs female | 0.77 (0.30–1.98) | .59 | ||
ALT | Increase per U/L | 1.000 (0.999–1.001) | .82 | ||
ALT, U/L | <2×, 2-5 ×, and >5 × ULN | 0.94 (0.55–1.63) | .83 | ||
Total bilirubin | Increase per mg/dL | 1.01 (0.81–1.26) | .93 | ||
Prior interferon use | Yes vs no | 0.28 (0.04–2.08) | .21 | ||
HBV DNA at baseline | Increase per 1 unit | 0.68 (0.50–0.92) | .012 | ||
HBV genotype, C vs B | C vs B | 0.90 (0.30–2.69) | .85 | ||
Platelet | Increase per 103/μL | 1.000 (0.992–1.009) | .92 | ||
FIB-4 index | Increase per 1 unit | 1.01 (0.90–1.14) | .83 | ||
HBsAg at baseline | Increase per log10 IU/mL | 0.26 (0.15–0.46) | <.001 | ||
HBsAg at 12 mo of treatment | Increase per log10 IU/mL | 0.18 (0.09–0.36) | <.001 | ||
Groups | Discontinued vs continued | 4.53 (1.52–13.56) | .007 | 5.27 (1.72–16.14) | .004 |
End of treatment (discontinued group) or 3 y of treatment (continued group) | |||||
Age, per y | Increase per y | 1.03 (0.99–1.08) | .19 | ||
ALT, U/L | Increase per U/L | 0.97 (0.92–1.01) | .14 | ||
Total bilirubin, mg/dL | Increase per mg/dL | 0.38 (0.07–1.92) | .24 | ||
FIB-4 index, per 1 unit | Increase per 1 unit | 1.17 (0.72–1.92) | .53 | ||
HBsAg, per log10 IU/mL | Increase per log10 IU/mL | 0.12 (0.06–0.23) | <.001 | 0.11 (0.05–0.21) | <.001 |
HBsAg, <150 vs ≥150 IU/mL | Yes vs no | 14.04 (5.06–38.97) | <.001 | ||
HBsAg decline from baseline | Increase per log10 IU/mL | 1.32 (0.66–2.46) | .47 | ||
Consolidation duration, per wk | Increase per wk | 1.012 (1.001–1.022) | .025 | ||
≥78 vs <78 wk | 0.84 (0.11–6.56) | .87 | |||
≥104 vs <104 wk | 0.81 (0.23–2.87) | .75 | |||
≥130 vs <130 wk | 0.82 (0.33–2.04) | .66 |
Variable | Comparison | Univariate Analysis | Multivariate Analysis | ||
HR (95% CI) | P value | HR (95% CI) | P value | ||
Start entecavir treatment | |||||
Age | Increase per y | 1.03 (0.98–1.08) | .22 | ||
Sex | Male vs female | 0.77 (0.30–1.98) | .59 | ||
ALT | Increase per U/L | 1.000 (0.999–1.001) | .82 | ||
ALT, U/L | <2×, 2-5 ×, and >5 × ULN | 0.94 (0.55–1.63) | .83 | ||
Total bilirubin | Increase per mg/dL | 1.01 (0.81–1.26) | .93 | ||
Prior interferon use | Yes vs no | 0.28 (0.04–2.08) | .21 | ||
HBV DNA at baseline | Increase per 1 unit | 0.68 (0.50–0.92) | .012 | ||
HBV genotype, C vs B | C vs B | 0.90 (0.30–2.69) | .85 | ||
Platelet | Increase per 103/μL | 1.000 (0.992–1.009) | .92 | ||
FIB-4 index | Increase per 1 unit | 1.01 (0.90–1.14) | .83 | ||
HBsAg at baseline | Increase per log10 IU/mL | 0.26 (0.15–0.46) | <.001 | ||
HBsAg at 12 mo of treatment | Increase per log10 IU/mL | 0.18 (0.09–0.36) | <.001 | ||
Groups | Discontinued vs continued | 4.53 (1.52–13.56) | .007 | 5.27 (1.72–16.14) | .004 |
End of treatment (discontinued group) or 3 y of treatment (continued group) | |||||
Age, per y | Increase per y | 1.03 (0.99–1.08) | .19 | ||
ALT, U/L | Increase per U/L | 0.97 (0.92–1.01) | .14 | ||
Total bilirubin, mg/dL | Increase per mg/dL | 0.38 (0.07–1.92) | .24 | ||
FIB-4 index, per 1 unit | Increase per 1 unit | 1.17 (0.72–1.92) | .53 | ||
HBsAg, per log10 IU/mL | Increase per log10 IU/mL | 0.12 (0.06–0.23) | <.001 | 0.11 (0.05–0.21) | <.001 |
HBsAg, <150 vs ≥150 IU/mL | Yes vs no | 14.04 (5.06–38.97) | <.001 | ||
HBsAg decline from baseline | Increase per log10 IU/mL | 1.32 (0.66–2.46) | .47 | ||
Consolidation duration, per wk | Increase per wk | 1.012 (1.001–1.022) | .025 | ||
≥78 vs <78 wk | 0.84 (0.11–6.56) | .87 | |||
≥104 vs <104 wk | 0.81 (0.23–2.87) | .75 | |||
≥130 vs <130 wk | 0.82 (0.33–2.04) | .66 |
Abbreviations: ALT, alanine aminotransferase, CI, confidence interval; FIB-4, fibrosis 4; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; HR, hazard ratio.
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