Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.
Department of Biomedical Research Center, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.
Clin Mol Hepatol. 2017 Sep;23(3):230-238. doi: 10.3350/cmh.2017.0003. Epub 2017 Jun 30.
BACKGROUND/AIMS: Tenofovir disoproxil fumarate (TDF) monotherapy for 48 weeks provided a virological response comparable to that of TDF and entecavir (ETV) combination therapy in patients infected with ETV-resistant hepatitis B virus (HBV). Little long-term data in routine clinical practice are available regarding the optimal treatment of patients with ETV-resistant HBV.
We investigated the long-term antiviral efficacy of combination therapy of TDF+lamivudine (LAM) or TDF+ETV compared to that of TDF monotherapy in 73 patients with resistance to both LAM and ETV.
Patients were treated with TDF monotherapy (n=12), TDF+LAM (n=19), or TDF+ETV (n=42) for more than 6 months. The median duration of TDF-based rescue therapy was 37 months. Virologic response (VR) was found in 63 patients (86.3%). The rates of VR among the three groups (TDF monotherapy, TDF+LAM, and TDF+ETV) were not statistically different (log-rank =0.200) at 12 months (59.3%, 78.9%, and 51.8%, respectively) or at 24 months (88.4%, 94.7%, and 84.2%). In addition, treatment efficacy of TDF-based combination or TDF monotherapy was not statistically different with ETV-resistant strains or exposure to other antiviral agents. In multivariate analysis, only lower baseline HBV DNA level was an independent predictor for VR (hazard ratio, 0.723; 95% confidence interval, 0.627-0.834; <0.001).
TDF monotherapy was as effective as combination therapy of TDF+LAM or TDF+ETV in maintaining long-term viral suppression in chronic hepatitis B patients with resistance to both LAM and ETV. HBV DNA level at the start of TDF rescue therapy was the only independent predictor of subsequent VR.
背景/目的:替诺福韦二吡呋酯(TDF)单药治疗 48 周提供了与 TDF 和恩替卡韦(ETV)联合治疗相比相当的病毒学应答,在感染 ETV 耐药乙型肝炎病毒(HBV)的患者中。在常规临床实践中,关于 ETV 耐药 HBV 患者的最佳治疗方法,可用的长期数据很少。
我们研究了 TDF+拉米夫定(LAM)或 TDF+ETV 联合治疗与 TDF 单药治疗对 73 例 LAM 和 ETV 双重耐药患者的长期抗病毒疗效。
12 例患者接受 TDF 单药治疗,19 例患者接受 TDF+LAM 治疗,42 例患者接受 TDF+ETV 治疗,疗程均超过 6 个月。基于 TDF 的挽救治疗中位持续时间为 37 个月。63 例患者(86.3%)获得病毒学应答(VR)。三组(TDF 单药治疗、TDF+LAM 和 TDF+ETV)在 12 个月(分别为 59.3%、78.9%和 51.8%)和 24 个月(分别为 88.4%、94.7%和 84.2%)时的 VR 率无统计学差异(对数秩检验=0.200)。此外,TDF 联合或 TDF 单药治疗的疗效与 ETV 耐药株或暴露于其他抗病毒药物无关。多变量分析表明,只有较低的基线 HBV DNA 水平是 VR 的独立预测因素(危险比,0.723;95%置信区间,0.627-0.834;<0.001)。
TDF 单药治疗与 TDF+LAM 或 TDF+ETV 联合治疗在维持对 LAM 和 ETV 均耐药的慢性乙型肝炎患者的长期病毒抑制方面同样有效。TDF 挽救治疗开始时的 HBV DNA 水平是随后 VR 的唯一独立预测因素。