[1]Du Jeong I, Jung S W, Park B R, et al. Clinicalcourse of partial virologic response with prolonged tenofovir therapy in nuclos(t)ides-nave patients with chronic hepatitis B. Dig Dis Sci, 2017, 62(10):2908-2914. [2]Lovett G C, Nguyen T, Iser D M, et al. Efficacy and safety of tenofovir in chronic hepatitis B: Australian real world experience. World J Hepatol, 2017, 9(1):48-56. [3]Okuda CH. Challenges of hepatitis B in the era of antiviral therapy. J Gastroenterol Hepatol, 2018, 34(3):501-506. [4]Sun Y, Wu X, Zhou J, et al. Persistent low level of hepatitis B virus promotes fibrosis progression during therapy. Clin Gastroenterol H, 2020, 18(11):2582-2591. [5]路正昭, 孙亚朦, 尤红. 慢性乙型肝炎低病毒血症致肝纤维化与肝细胞癌. 中华肝脏病杂志,2021, 29(12):1144-1146. [6]Nam J Y, Chang Y, Cho H, et al. Delayed viral suppression during antiviral therapy is associated with increased hepatocellular carcinoma rates in HBeAg-positive high viral load chronic hepatitis B. J Viral Hepat, 2018, 25(5):552-560. [7]Kim J H, Sinn D H, Kang W, et al. Low-level viremia and the increased risk of hepatocellular carcinoma in patients receiving entecavir treatment. Hepatology, 2017, 66(2): 335-343. [8]Terrault N A, McMahon B J, Chang K M, et al. Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance. Clin Liver Dis, 2018, 67(4):1560-1599. [9]中华医学会感染病学分会, 中华医学会肝病学分会. 慢性乙型肝炎防治指南(2019年版). 实用肝脏病杂志, 2020, 23(1):9-32. [10] 中国肝炎防治基金会, 中华医学会感染病学分会, 中华医学会肝病学分会和中国研究型医院学会肝病专业委员会. 瞬时弹性成像技术诊断肝纤维化专家共识(2018年更新版). 中华肝脏病杂志, 2019, 27(3):182-191. [11] 鲁凤民, 封波, 郑素军, 等. 核苷(酸)类似物经治的慢性乙型肝炎患者低病毒血症的研究现状. 临床肝胆病杂志, 2021, 37(6): 1268-1274. [12] Song J E, Lee C H, Kim B S. Efficacy of long-term tenofovir disoproxil fumarate therapy in chronic hepatitis B patients with partial virologic response in real practice. Korean J Intern Med, 2019, 34(4): 802–810. [13] Cho J Y, Sohn W, Sinn D H,et al. Long-term real-world entecavir therapy in treatment-nave hepatitis B patients: base-line hepatitis B virus DNA and hepatitis B surface antigen levels predict virologic response. Korean J Intern Med, 2017, 32(4):636-646. [14] Wong L H , Wong W S , Chan H Y , et al. Undetectable HBV DNA at month 12 ofentecavir treatment predicts maintained viral suppression and HBeAg-seroconversion in chronic hepatitis B patients at 3 years. Aliment Pharm Ther, 2012, 35(11):1326-1335. [15] Yim H J, Kim I H, Suh S J, et al. Switching to tenofovir vs continuingentecavir for hepatitis B virus with partial virologic response to entecavir: a randomized controlled trial. J Viral Hepat, 2018, 25(11):1321-1330. [16] Wang Y H, Liao J, Zhang D M, et al. Tenofovir monotherapy versus tenofovir plusentecavir combination therapy in HBeAg-positive chronic hepatitis patients with partial virological response to entecavir. J Med Virol, 2020, 92(3):302-308. [17] Nguyen M H, Atsukawa M, Ishikawa T, et al. Outcomes ofsequential therapy with tenofovir alafenamide after long-term entecavir. Am J Gastroenterol, 2021, 116(6):1264-1273. [18] Ogawa E, Nomura H, Nakamuta M, et al. Tenofovir alafenamide after switching from entecavir or nucleos(t)ide combination therapy for patients with chronic hepatitis B. Liver Int, 2020, 40(7):1578-1589. [19] Li Z B, Li L, Niu X X, et al. Switching from entecavir to tenofovir alafenamide for chronic hepatitis B patients with low-level viraemia. Liver Int, 2021, 41(6):1254-1264. [20] 中华医学会肝病学分会. 扩大慢性乙型肝炎抗病毒治疗的专家意见. 中华肝脏病杂志, 2022, 30(2): 131-136. [21] Hudu S A, Niazlin M T, Nordin S A, et al. Quantitativehepatitis B e antigen: a better predictor of hepatitis B virus DNA than quantitative hepatitis B surface antigen. Clin Lab, 2018, 64(4):443-449. [22] 曹辉, 张玮. 核苷(酸)类药物治疗慢性乙型肝炎患者影响HBeAg血清转换的免疫学因素研究进展. 实用肝脏病杂志, 2017, 20(3):372-376. |