Pediatric Liver Diseases Therapy and Research Center, Beijing 302 Hospital, Beijing 100039, China.
Department of Medical Statistics, Academy of Military Medical Sciences, Beijing 100850, China.
J Hepatol. 2018 Jun;68(6):1123-1128. doi: 10.1016/j.jhep.2018.01.037. Epub 2018 Feb 13.
BACKGROUND & AIM: Chronic infection with hepatitis B virus (HBV) in children is a serious health problem worldwide. How to treat children with immune-tolerant chronic hepatitis B infection, commonly characterized by hepatitis B e antigen (HBeAg) positivity, high viral load, normal or mildly elevated alanine aminotransferase and no or minimal inflammation in liver histology, remains unresolved. This trial aims to study the benefits of antiviral therapy in children with these characteristics.
This is a pilot open-label randomized controlled study. From May 2014 to April 2015, 69 treatment-naive chronically HBV-infected children, aged 1 to 16 years, who had immune-tolerant characteristics were recruited to this trial and randomly assigned, in a 2:1 ratio, to treatment group and control group. Patients in the treatment group received either interferon-α (IFN) monotherapy or consecutively received IFN monotherapy, combination therapy of IFN and lamivudine (LAM), and LAM therapy alone. All patients were observed until week 96.
At baseline, epidemiological, biochemical, serological, virological and histological indices were consistent across the treatment and control groups. Of the 46 patients in the treatment group, 73.91% had undetectable serum HBV DNA, 32.61% achieved HBeAg seroconversion and 21.74% lost hepatitis B surface antigen (HBsAg) at the endpoint. No LAM resistance emerged at week 96. In the control group, only one (4.35%) patient underwent spontaneous HBeAg seroconversion and had undetectable serum HBV DNA during observation, and moreover, none developed HBsAg clearance. For all patients, no serious adverse events were observed.
Antiviral treatment with a sequential combination of IFN and LAM resulted in a significant improvement in the rates of undetectable serum HBV DNA, HBeAg seroconversion and HBsAg loss in children with chronic HBV infection and immune-tolerant characteristics.
There is a lack of data regarding treatment of immune-tolerant chronic hepatitis B (CHB). It remains unresolved how children with immune-tolerant CHB should be treated. This paper reports the outcomes from a pilot open-label randomized controlled trial on antiviral therapy in children with immune-tolerant characteristics. It shows that a sequential combination of interferon-α and lamivudine was beneficial.
乙型肝炎病毒(HBV)慢性感染是全世界严重的健康问题。如何治疗乙型肝炎 e 抗原(HBeAg)阳性、病毒载量高、丙氨酸氨基转移酶正常或轻度升高、肝组织学无或轻度炎症的免疫耐受慢性乙型肝炎感染患儿,仍未解决。本试验旨在研究这些特征患儿抗病毒治疗的益处。
这是一项开放性标签随机对照研究的初步研究。2014 年 5 月至 2015 年 4 月,我们招募了 69 例未经治疗的慢性 HBV 感染儿童,年龄 1 至 16 岁,具有免疫耐受特征,按照 2:1 的比例随机分为治疗组和对照组。治疗组患者接受干扰素-α(IFN)单药治疗或序贯接受 IFN 单药治疗、IFN 联合拉米夫定(LAM)联合治疗和 LAM 单药治疗。所有患者均观察至第 96 周。
在基线时,治疗组和对照组的流行病学、生化、血清学、病毒学和组织学指标一致。在治疗组的 46 例患者中,73.91%的患者血清 HBV DNA 不可检测,32.61%的患者 HBeAg 血清学转换,21.74%的患者在终点时失去乙型肝炎表面抗原(HBsAg)。第 96 周时未出现 LAM 耐药。在对照组中,只有 1 例(4.35%)患者自发发生 HBeAg 血清学转换,在观察期间血清 HBV DNA 不可检测,而且无一例患者 HBsAg 清除。所有患者均未发生严重不良事件。
在具有免疫耐受特征的慢性 HBV 感染儿童中,采用 IFN 与 LAM 序贯联合的抗病毒治疗可显著提高血清 HBV DNA 不可检测率、HBeAg 血清学转换率和 HBsAg 丢失率。
对于免疫耐受慢性乙型肝炎(CHB)的治疗,目前数据较少。对于免疫耐受 CHB 患儿,应如何治疗,仍未解决。本文报告了一项针对免疫耐受特征儿童抗病毒治疗的初步开放性标签随机对照试验结果。结果表明,干扰素-α与拉米夫定序贯联合治疗有益。