SERUM HBEAG QUANTITATION DURING ANTIVIRAL THERAPY FOR CHRONIC HEPATITIS-B

Hepatitis Be antigen (HBeAg) seroconversion is considered the principa l short-term goal of antiviral therapy in chronic hepatitis B. To test whether the pre-and per-treatment HBeAg quantitation has a higher pre dictive value than that of hepatitis B virus DNA (HBV-DNA) quantitatio n for the outcome of antiviral therapy in chronic hepatitis B. A quant itative measurement of HBV-DNA and HBeAg (AxSYM HBe 2.0 Quantitative, Abbott Laboratories) was undertaken in serial serum samples from 30 pa tients with 16-week interferon-alpha (IFN-alpha) treatment (follow-up 36 weeks; 14 responders) and from 15 patients with 24-week lamivudine treatment (follow-up 24 weeks; 2 responders). In the group of interfer on-treated patients, the median pretreatment HBV-DNA level was signifi cantly lower in responders compared to nonresponders (P = 0.02); the d ifference in median HBeAg level was not significant. However, the perc entage of response was significantly related (P = 0.003) to the magnit ude of decline in HBeAg level between the start of therapy and week 4. This phenomenon was not observed for HBV-DNA. Using multivariate anal ysis, it was found that the fall of HBeAg levels between weeks 0 and 4 was the most important independent predictor of response. In the grou p of lamivudine treated patients, the rapid decline in HBV-DNA (>90%) in 12 patients at week 4 had no relation to HBeAg seroconversion. In c ontrast, the fall in HBeAg-level (one patient with >50% reduction at w eek 4 seroconverted) appears to be predictive. Quantitation of HBeAg a t start and early during therapy may have clinically important predict ive value for long-term response to antiviral therapy. (C) 1997 Wiley- Liss, Inc.