Early serum HBsAg level as a strong predictor of sustained response to peginterferon alfa‐2a in HBeAg‐negative chronic hepatitis B

Abstract

The roles remain unclear of early on-treatment quantitative serum HBsAg and hepatitis B virus (HBV) DNA levels in the prediction of a sustained response (SR) to peginterferon alfa-2a therapy in HBeAg-negative chronic hepatitis B (CHB) patients infected with genotype B or C. To determine their roles in HBeAg-negative CHB patients infected with genotype B or C. Sixty-one patients were treated with peginterferon alfa-2a for 48weeks. Serum HBsAg levels were quantified using the Abbott Architect HBsAg QT assay throughout treatment. Multiple regression analyses were performed to identify independent predictors of SR. Nineteen patients (31%) achieved SR with serum HBV DNA levels <312copies/mL at 24weeks post-treatment. Serum HBsAg levels at 12 (OR 31.9; 95% CI 4.8-209.6; P=0.0003) and 24weeks of therapy (OR 8.8; 95% CI 2.0-38.0; P=0.0035), and HBV DNA levels at baseline (OR 7.0; 95% CI 1.3-36.2; P=0.0203), 12 (OR 7.9; 95% CI 1.2-48.4; P=0.0249) and 24weeks of therapy (OR 22.3; 95% CI 2.2-224.0; P=0.0083) were early independent predictors of SR. A serum HBsAg cut-off of 150IU/mL at week 12 had an AUC, sensitivity, specificity and positive and negative predictive values of 0.75, 63%, 95%, 86% and 85% with respect to predicting SR respectively. A quantitative serum HBsAg level at 12weeks of therapy can be used for the early prediction of SR to peginterferon therapy in HBeAg-negative CHB patients infected with genotype B or C.