Department of Infectious Diseases, Children's Hospital of Fudan University, Shanghai, 201102, China.
World J Pediatr. 2019 Dec;15(6):595-600. doi: 10.1007/s12519-019-00303-w. Epub 2019 Sep 5.
Interferon alpha (IFN-α) is a preferred therapy for antiviral treatment of children with chronic hepatitis B (CHB) aged > 1 year currently. Peginterferon alpha-2a (Peg-IFN α-2a) is a recommended international guideline for treatment of CHB children, which is limited to children aged > 3 years. But the exact efficacy and safety of IFN-α and Peg-IFN α-2a for treating CHB are not sufficient.
Clinical manifestations, baseline characteristics, related laboratory tests and adverse events were retrospectively analyzed in children with CHB, who visited Children's Hospital of Fudan University and were treated with IFN α-2b or Peg-IFN α-2a monotherapy and followed up from January 2003 to October 2018.
A total of 36 immune-active patients without advanced fibrosis were enrolled to be treated with IFN α-2b (group A, n = 18) or Peg-IFN α-2a (group B, n = 18). IFN α-2b or Peg-IFN α-2a was administered for a median of 48 weeks subcutaneously by body surface area (BSA) category at a dose of 3 MU/m or 104 μg/m, respectively. HBV e antigen (HBeAg) seroconversion rates at 48 weeks post-treatment were higher in group A than group B (92.9% vs. 87.5%), so as the rates of HBsAg clearance (22.2% vs. 11.1%), and hepatitis B virus (HBV)-DNA < 1000 IU/mL (88.9% vs. 83.3%). Only mild flu-like symptoms and transient neutropenia appeared in some children at the early stage of treatment. No severe abnormal results was observed in other laboratory assessments.
The antiviral monotherapy of 48-week IFN α-2b or Peg-IFN α-2a in children with CHB is well tolerated and effective, which is associated with higher rates of HBeAg seroconversion and HBsAg clearance than in adults and previously pediatric patients.
干扰素 alpha(IFN-α)是目前治疗> 1 岁儿童慢性乙型肝炎(CHB)的首选抗病毒治疗方法。聚乙二醇干扰素 alpha-2a(Peg-IFN α-2a)是治疗 CHB 儿童的国际推荐指南,仅适用于> 3 岁的儿童。但是,IFN-α和 Peg-IFN α-2a 治疗 CHB 的确切疗效和安全性尚不足。
回顾性分析 2003 年 1 月至 2018 年 10 月在复旦大学附属儿科医院就诊并接受 IFN-α-2b 或 Peg-IFN α-2a 单药治疗的 CHB 儿童的临床表现、基线特征、相关实验室检查和不良事件。
共纳入 36 例无晚期纤维化的免疫活性患者,分别接受 IFN-α-2b(A 组,n = 18)或 Peg-IFN α-2a(B 组,n = 18)治疗。A 组和 B 组儿童按体表面积(BSA)类别皮下给予 IFN-α-2b 或 Peg-IFN α-2a,剂量分别为 3 MU/m 和 104 μg/m,疗程均为 48 周。治疗后 48 周时,A 组 HBeAg 血清学转换率(92.9%比 87.5%)和 HBsAg 清除率(22.2%比 11.1%)均高于 B 组,HBV-DNA<1000 IU/mL 率(88.9%比 83.3%)也高于 B 组。仅少数患儿在治疗早期出现轻度流感样症状和短暂性中性粒细胞减少症,其他实验室检查未见严重异常。
48 周 IFN-α-2b 或 Peg-IFN α-2a 单药治疗 CHB 儿童的抗病毒疗效和安全性良好,HBeAg 血清学转换率和 HBsAg 清除率均高于成人和既往儿科患者。