Interferon alpha has been used widely to treat hepatitis B virus infection
in children. However, the overall initial response rates have been <50% and
several strategies have been attempted to improve this. The aim of this st
udy was to evaluate the safety and efficacy of prolonged interferon <alpha>
treatment in children who did not respond to a previous course of interfer
on alpha treatment. Twenty-seven children with chronic hepatitis B who had
not responded to a 6-month course of interferon alpha 2a (5 MU/m(2) body su
rface) thrice weekly subcutaneously continued to receive interferon aat the
same dosage for another 6 months without a rest phase. The children were f
ollowed for 6 months after completing 12 months of therapy. All of them had
HBsAg, HBV-DNA and HBeAg tested on completion of the first course. Six of
the 27 (22.2%) cleared both HBV-DNA and HBeAg after completion of therapy a
nd all six had a sustained response. Pre-treatment predictive factors were
not significantly associated with treatment response. No adverse effect of
interferon was seen during follow-up. We conclude that prolonged interferon
treatment is well tolerated and leads to additional benefit.