Treatment of chronic hepatitis B in children with prednisone followed by alfa-interferon: a controlled randomized
R Utili1, E Sagnelli, G B Gaeta
1Institute of Medical Therapy, University of Naples, 2nd Medical School, Italy.
Insights
Sequential treatment with prednisone and interferon showed efficacy in clearing hepatitis B virus markers in children with chronic hepatitis B. Lower baseline viral DNA levels predicted successful HBeAg clearance, suggesting a targeted treatment approach.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Virology
Background:
- Chronic hepatitis B (CHB) in children requires effective treatment strategies.
- Hepatitis B e-antigen (HBeAg) and hepatitis B virus DNA (HBV-DNA) are key markers of viral replication and infectivity.
Purpose of the Study:
- To evaluate the efficacy and safety of sequential prednisone and interferon alfa-2a treatment in children with CHB.
- To assess the impact of baseline viral load on treatment outcomes.
Main Methods:
- A randomized controlled study involving 43 children with biopsy-proven CHB.
- Treatment group received 1 month of prednisone followed by 12 months of interferon alfa-2a.
- Control group received no treatment.
Main Results:
- HBeAg seroconversion and HBV-DNA clearance occurred in 41% of treated patients versus 9.5% of controls (p=0.020).
- Two treated patients achieved HBsAg clearance.
- Stable normal alanine aminotransferase levels were observed in 59% of treated patients.
- Baseline HBV-DNA <100 pg/ml predicted 75% HBeAg clearance; no clearance occurred with levels >100 pg/ml.
Conclusions:
- Sequential prednisone and interferon alfa-2a is a safe and effective treatment for inducing HBeAg clearance in children with CHB and low viral replication.
- The regimen appears ineffective for children with high viral replication levels.
Abstract:
The efficacy and safety of sequential treatment with prednisone and interferon was evaluated in a randomized, controlled study on 43 children with biopsy proven HBsAg/HBeAg/hepatitis B virus-DNA positive, anti-delta negative, chronic hepatitis (34 chronic persistent hepatitis, 9 chronic active hepatitis). Patients received either a 1-month course of prednisone (0.6 to 0.3 mg/kg per day) followed by interferon alfa-2a (3 MU/m2, thrice weekly, for 12 months; 22 patients) or no treatment (21 patients). At the end of the study (20 months), clearance of hepatitis B virus-DNA and HBeAg seroconversion were observed in nine (41%) of the patients treated with prednisone and interferon and in two (9.5%) of the untreated controls (p = 0.020). Two of the treated patients who lost HBeAg, also cleared HBsAg. In the treated group, 13 (59%) patients had stable normal levels of alanine aminotransferase on their last examination. The baseline serum level of hepatitis B virus-DNA was an important predictor of response. In fact, HBeAg clearance was observed in 75% of patients with a baseline hepatitis B virus-DNA level lower than 100 pg/ml and in none with a level above 100 pg/ml. We suggest that combined treatment with prednisone followed by alfa-interferon may be safe and effective in inducing a stable clearance of HBeAg and, in some cases, of HBsAg in children with chronic hepatitis B and with a low level of viral replication. For children with high levels of viral replication, this regimen seems to be ineffective.
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