Clinical course of patients with insufficient viral suppression during entecavir therapy in genotype C chronic hepatitis B

被引:17
|
作者
Bang, Sung-Jo [1 ]
Kim, Byung Gyu [1 ]
Shin, Jung Woo [1 ]
Ju, Hyeong Uk [1 ]
Park, Bo Ryung [2 ]
Kim, Min-Ho [2 ]
Kim, Chang Jae [2 ]
Park, Jae Ho [1 ]
Jeong, In Du [1 ]
Jung, Seok Won [1 ]
Park, Neung Hwa [1 ,2 ]
机构
[1] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Dept Internal Med, Ulsan 680749, South Korea
[2] Univ Ulsan, Biomed Res Ctr, Coll Med, Ulsan Univ Hosp, Ulsan 680749, South Korea
基金
新加坡国家研究基金会;
关键词
Chronic hepatitis B; Entecavir; Partial virologic response; Primary non-response; VIROLOGICAL BREAKTHROUGH; NAIVE PATIENTS; RESISTANCE; LAMIVUDINE; ADHERENCE;
D O I
10.1016/j.dld.2012.12.013
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The clinical course of patients with insufficient virologic suppression diagnosed with chronic hepatitis B undergoing entecavir therapy is unclear. Methods: We retrospectively investigated the long-term clinical outcomes of entecavir treatment for more than 12 months in 355 nucleos(t) ide-naive chronic hepatitis B patients, particularly those with primary non-response or partial virologic response. Results: The median duration of entecavir therapy was 40 months (range, 12-64 months). Virologic response was achieved in 315 patients (88.7%). One hundred forty-four (96.6%) of 149 HBeAg-negative patients achieved virologic response. Among 206 HBeAg-positive patients, 52 (25.2%) achieved HBeAg seroconversion. Virologic breakthrough was observed in 7 patients (2.0%). Of these 7 patients, 5 (1.4%) had genotypic resistance to entecavir. Primary non-response and partial virologic response were evident in 6 (1.7%) and 63 (17.7%) patients, respectively. During continuous prolonged entecavir therapy, virologic response of patients with primary non-response and partial virologic response was achieved in 6 (100%) and 28 (44.4%) patients, respectively. Conclusion: The vast majority of chronic hepatitis B patients in this study achieved virologic response through prolonged entecavir therapy, with only 1.4% chance of viral resistance. Furthermore, all patients with primary non-response were able to achieve virologic response without adjustment of antiviral therapy. (c) 2012 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:600 / 605
页数:6
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