摘要

Aim: This study evaluated the on-treatment serum hepatitis B surface antigen (HBsAg) level during nucleos(t)ide analog (NUC) therapy and the correlation with off-treatment sustained virological response (SVR). Methods: Fifty-one consecutive patients with hepatitis B e-antigen (HBeAg) positive chronic hepatitis B who achieved HBeAg loss/seroconversion after NUC therapy and completed 12months or more of additional therapy were included. Serum HBsAg and hepatitis B virus (HBV) DNA levels were determined at baseline, 3, 6, 9 and 12months, and at the end of treatment. SVR was defined as HBV DNA levels of less than 10000 copies/mL until 6 or 12months off-treatment without reappearance of HBeAg. Results: Twenty-two (43.1%) and 13 (25.5%) patients maintained SVR at 6 and 12months off-treatment, respectively. In univariate analyses, a decline of HBsAg of 0.5log10IU/mL or less at 6months (P=0.006) and 12months (P=0.013), the mean change in HBsAg level at 6months (P=0.024), and lamivudine or entecavir treatment (P=0.019) were significant predictive factors for SVR at 6months off-treatment. A decline of HBsAg of 0.5log10IU/mL or less at 6months and lamivudine or entecavir treatment were independent factors on multivariate analyses (odds ratio [OR], 16.67; 95% confidence interval [CI], 1.86142.86 [P=0.012]; and OR, 14.83; 95% CI, 1.18185.73 [P=0.036]; respectively). Conclusion: On-treatment serum HBsAg level predicted early off-treatment SVR to NUC therapy in patients infected with genotype C.

  • 出版日期2013-3

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