Department of Pediatrics, Kyungpook National University School of Medicine, Daegu, Korea.
J Pediatr Gastroenterol Nutr. 2012 Dec;55(6):648-52. doi: 10.1097/MPG.0b013e318262a737.
The aim of the study was to compare the virologic response to adefovir (ADV) add-on therapy with switching to entecavir (ETV) monotherapy in children and adolescents with chronic hepatitis B (CHB) who have developed lamivudine (LAM) resistance during LAM treatment.
Twenty-seven consecutive patients with CHB who had developed LAM resistance during LAM treatment were included. Of these 27 patients, 8 patients were treated with the addition of ADV to ongoing LAM and 8 patients were treated by switching to ETV monotherapy and each of these 16 patients were compared with the 11 patients who were treated by switching to ADV alone, as a historical control. Therapeutic responses to treatment were evaluated at 12, 24, 36, and 48 weeks from the initiation of therapy by measuring the decrement of hepatitis B virus (HBV)-DNA titers.
The therapeutic period for HBV-DNA titer decrement (>2 log(10) IU/mL) was significantly shorter in both the LAM+ADV group and the ETV group than in the ADV group (P = 0.008); however, there was no significant difference between the LAM+ADV group and the ETV group. The rate of virologic response, defined as decrement in HBV-DNA titer to undetectable levels at 24 weeks, was significantly higher in both the LAM+ADV group and the ETV group than in the ADV group (P = 0.029).
Both the LAM+ADV combination therapy and ETV monotherapy exhibited significantly more effective virologic responses compared to the ADV monotherapy in children and adolescents with LAM-resistant CHB, although there was no significant difference between the LAM+ADV group and the ETV group.
本研究旨在比较拉米夫定(LAM)耐药患者在 LAM 治疗过程中加用阿德福韦酯(ADV)或换用恩替卡韦(ETV)单药治疗的病毒学应答。
共纳入 27 例在 LAM 治疗过程中发生 LAM 耐药的慢性乙型肝炎(CHB)患儿和青少年。其中 8 例患者加用 ADV 治疗,8 例换用 ETV 单药治疗,与 11 例单独换用 ADV 治疗的患者进行比较。从开始治疗的 12、24、36 和 48 周时,通过测量乙型肝炎病毒(HBV)DNA 滴度的下降来评估治疗反应。
在 LAM+ADV 组和 ETV 组中,HBV-DNA 滴度下降(>2 log10 IU/ml)的治疗时间明显短于 ADV 组(P=0.008),但 LAM+ADV 组和 ETV 组之间无显著差异。在 LAM+ADV 组和 ETV 组中,病毒学应答(定义为 24 周时 HBV-DNA 滴度下降至不可检测水平)的比例显著高于 ADV 组(P=0.029)。
在 LAM 耐药的 CHB 患儿和青少年中,与 ADV 单药治疗相比,LAM+ADV 联合治疗和 ETV 单药治疗均表现出更有效的病毒学应答,尽管 LAM+ADV 组和 ETV 组之间无显著差异。