| Objective:Follow-up48weeks clinical outcome of patients with eantigen positive chronic hepatitis B after treated by pegylated interferonalpha-2a.Methods: A total of162patients were included in the study. Allpatients with e antigen positive chronic hepatitis B receiving180gpeginterferon alfa-2a once-weekly for48weeks. During the48weekstreatment,the analine aminotransferase(ALT), white blood cell (WBC),platelet (PLT) were examined once every4weeks, and responses includingHBsAg, HBeAg seroconversion and HBV DNA suppression were measuredonce every12weeks,and abdominal ultrasoundã€AFP were examined everysix months. After the end of the48weeks of treatment, we followed up for48weeks again. During the period of48weeks follow-up, HBsAg, HBeAgseroconversion and HBV DNA suppression were measured once every12weeks,and abdominal ultrasoundã€AFP were examined every six months.Results: Mean HBV DNA level at baseline was (6.58±0.90) log10copies/mL. At the end of the48weeks post-treatment sustained HBeAgseroconversion was achieved by40.12%(65/162),41.98%(68/162) patients developed virological response HBV-DNA.1patients sustaintedHBsAg seroconversion. During the follow-up of48weeks,seventy patients(70/162,43.21%)had hepatitis B surface antigen(HBsAg) seroconversionand fifty-nine(59/162,36.42%)patients developed virological responseHBV-DNA. But there are ten patients(10/162,6.17%) experiencedvirological rebound. No unexpected adverse events were reported.Conclusions: Pegylated interferon alpha-2a can sustain the serologicalHBeAg stable conversion at the end of treatment,and suppression ofHBV-DNA replication.But there are a few patient with virological reboundafter the end of treatment. The baseline ALT level, age, virological responsetime, baseline quantitative level of HBV-DNA had no significantrelationship between the virological rebound. |