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. 2013 Dec;59(6):1153-9.
doi: 10.1016/j.jhep.2013.07.017. Epub 2013 Jul 18.

Response to peginterferon alfa-2a (40KD) in HBeAg-negative CHB: on-treatment kinetics of HBsAg serum levels vary by HBV genotype

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Response to peginterferon alfa-2a (40KD) in HBeAg-negative CHB: on-treatment kinetics of HBsAg serum levels vary by HBV genotype

Maurizia R Brunetto et al. J Hepatol. 2013 Dec.

Abstract

Background & aims: We investigated whether HBV genotype influences on-treatment HBsAg kinetics and/or the end-of-treatment HBsAg levels associated with long-term virological response in HBeAg-negative chronic hepatitis B patients treated with peginterferon alfa-2a±lamivudine in the Phase III trial.

Methods: All patients (n=230) who participated in long-term follow-up were included according to the availability of HBsAg level measurements. Long-term virological response was defined as HBV DNA ≤ 10,000cp/ml (1786IU/ml) at 5 years post-treatment. Genotype-specific end-of-treatment HBsAg levels associated with long-term virological response (identified by ROC analysis) were assessed in 199 patients with HBsAg measurements available at baseline and end-of-treatment. HBsAg kinetics according to genotype and long-term virological response were investigated in the 117 patients with additional samples available at weeks 12, 24, and 72.

Results: Baseline HBsAg levels were significantly higher for A than B, C, and D genotypes (p<0.05). On-treatment HBsAg kinetics varied according to HBV genotype. The difference between responders and non-responders was greatest for genotype A from weeks 12-24; for genotypes B and D from baseline to week 12; there was no significant difference over any timeframe for genotype C. High positive predictive values for long-term virological response could be obtained by applying end-of-treatment genotype-specific cut-offs: 75%, 47%, 71%, and 75% for genotypes A (<400IU/ml), B (<50IU/ml), C (<75IU/ml), and D (<1000IU/ml), respectively.

Conclusions: On-treatment HBsAg kinetics vary between HBV genotypes. Genotype-specific monitoring timeframes and end-of-treatment thresholds could ameliorate response-guided treatment of HBeAg-negative chronic hepatitis B.

Keywords: ALT; CHB; EOT; Genotype; HBV; HBeAg; HBeAg-negative chronic hepatitis B; HBsAg; HBsAg quantification; IFN; LVR; NPV; PPV; Peginterferon alfa-2a; ROC; Response-guided; alanine aminotransferase; chronic hepatitis B; end-of-treatment; hepatitis B e antigen; hepatitis B s antigen; hepatitis B virus; interferon; long-term virological response; negative predictive value; positive predictive value; receiver-operating characteristic.

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Comment in

  • Focus.
    Shouval D. Shouval D. J Hepatol. 2013 Dec;59(6):1151-2. doi: 10.1016/j.jhep.2013.09.005. Epub 2013 Sep 7. J Hepatol. 2013. PMID: 24021425 No abstract available.

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