Comparison of rescue strategies in lamivudine-resistant patients with chronic hepatitis B

被引:30
作者
Zhao, Pan [1 ]
Wang, Chunya [2 ]
Huang, Lili [1 ]
Xu, Dongping [1 ]
Li, Tanshi [2 ]
机构
[1] Beijing 302 Hosp, Liver Failure Therapy & Res Ctr, Beijing 100039, Peoples R China
[2] Beijing 301 Hosp, Gen Hosp PLA, Emergency Dept, Beijing 100853, Peoples R China
关键词
Chronic hepatitis B; Lamivudine; Resistance; Adefovir dipivoxil; Entecavir; ADEFOVIR DIPIVOXIL; IN-VITRO; THERAPY; ENTECAVIR; MUTANTS; REPLICATION; MONOTHERAPY; PREVALENCE; EMERGENCE;
D O I
10.1016/j.antiviral.2012.08.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lamivudine (LAM) resistance now poses a major problem in the management of patients with chronic hepatitis B virus (HBV) infection. We retrospectively collected clinical data on chronic HBV-infected patients who had developed LAM resistance under de novo LAM monotherapy and subsequently took nucleos(t)ide analogs as rescue strategy in our hospital. From initiation of rescue therapies to January 2012, incidence of antiviral drug resistance was 23.67%, 18%, 6.94% and 0% (P=0.007) in the group of switching to adefovir dipivoxil (ADV) monotherapy, switching to entecavir (ETV) monotherapy, adding on ADV and switching to combination of ADV and ETV. At month 12, the median levels of serum HBV DNA were respectively 9300 IU/mL, 4648 IU/mL, 2054 IU/mL and 100 IU/mL (P < 0.001), and the cumulative rates of serum ALT normalization were respectively 75%, 84%, 93% and 100% (P = 0.003). Additionally, the strategy of switching to ADV monotherapy induced more single rtA181T mutations. In conclusion, switching to ADV monotherapy has been widely used in real-world clinical practice in China, however, due to the high incidence of drug resistance, switching to neither ADV nor ETV monotherapy is optimal when LAM resistance occurs; combination of ADV and ETV is most effective, whereas the strategy of adding on ADV is rational for most of LAM-resistant Chinese patients with chronic hepatitis B. Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 104
页数:5
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