Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
J Clin Gastroenterol. 2012 Mar;46(3):243-50. doi: 10.1097/MCG.0b013e318225f559.
In this study, we aimed to devise a simple scoring system predicting the risk of genotypic resistance (GR) to current rescue therapies for patients with lamivudine (LAM)-resistant chronic hepatitis B.
LAM and adefovir (ADV) combination therapy should be recommended for an initial rescue therapy against LAM-resistant hepatitis B virus (HBV). However, there still are many LAM-resistant patients being treated with entecavir (ETV) or ADV monotherapy.
This retrospective cohort study included consecutive patients treated for LAM-resistant chronic hepatitis B with ETV or ADV monotherapy, or LAM/ADV combination therapy. The cumulative probabilities of GR and virological responses and breakthrough according to clinical variables were analyzed by survival analyses and derived an index for future GR.
A total of 224 patients were included (median treatment duration=117.9 wk). Using risk factors indentified on multivariable analyses, a simple index for future GR (Antiviral Resistance Prediction Index, ARPI) was developed with 3 clinical variables: the rescue therapy regimens (+0, ADV; +1, ETV; +2, LAM/ADV), HBV DNA reduction at 12 weeks (+0, <3 log10 copies/mL; +1, >3 log10 copies/mL), and the initial HBV DNA level (+0, >10 copies/mL; +1, <10 copies/mL). No patient with ARPI ≥2 exhibited GR, whereas 47% of the patients with an ARPI <2 developed GR by week 144 (P=0.005).
The results of this study suggest that the ARPI is a simple and early index that can be used to determine the risk for subsequent GR during rescue therapy for LAM-resistant chronic hepatitis B.
本研究旨在设计一种简单的评分系统,预测对拉米夫定(LAM)耐药慢性乙型肝炎患者当前挽救治疗的基因型耐药(GR)风险。
LAM 和阿德福韦(ADV)联合治疗应作为 LAM 耐药乙型肝炎病毒(HBV)的初始挽救治疗推荐。然而,仍有许多 LAM 耐药患者接受恩替卡韦(ETV)或 ADV 单药治疗。
本回顾性队列研究纳入了接受 ETV 或 ADV 单药或 LAM/ADV 联合治疗的 LAM 耐药慢性乙型肝炎连续患者。通过生存分析分析了根据临床变量的 GR 和病毒学应答以及突破的累积概率,并得出了未来 GR 的指标。
共纳入 224 例患者(中位治疗时间为 117.9 周)。使用多变量分析确定的危险因素,开发了一种简单的未来 GR 指标(抗病毒耐药预测指数,ARPI),包含 3 个临床变量:挽救治疗方案(+0,ADV;+1,ETV;+2,LAM/ADV)、12 周时 HBV DNA 降低(+0,<3 log10 拷贝/mL;+1,>3 log10 拷贝/mL)和初始 HBV DNA 水平(+0,>10 拷贝/mL;+1,<10 拷贝/mL)。ARPI≥2 的患者无一例出现 GR,而 ARPI<2 的患者中有 47%在第 144 周时出现 GR(P=0.005)。
这项研究的结果表明,ARPI 是一种简单且早期的指标,可用于确定 LAM 耐药慢性乙型肝炎挽救治疗期间后续 GR 的风险。