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Individual prediction model for lamivudine treatment response in hepatitis B virus e antigen-positive chronic hepatitis B patients

Authors
Lee, Hyun WoongKang, WonseokAhn, Sang HoonLee, Heon JuHwang, Jae SeokSohn, Joo HyunJang, Jae YoungHan, Ki JunKim, Ja KyungKim, Do YoungPaik, Yong HanLee, Chun KyonChoi, Ik-SeongLee, Kwan SikHan, Kwang-Hyub
Issue Date
May-2014
Publisher
WILEY
Keywords
chronic hepatitis B; lamivudine; treatment
Citation
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, v.29, no.5, pp.1049 - 1055
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
Volume
29
Number
5
Start Page
1049
End Page
1055
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160069
DOI
10.1111/jgh.12522
ISSN
0815-9319
Abstract
Background and AimsAlthough prolonged lamivudine (LAM) therapy is associated with the emergence of LAM-resistant mutations, it is still a commonly used therapy in many Asian countries because of its established long-term safety and low cost. The aim of our study was to assess the predictors of long-term LAM treatment response and to establish an individual prediction model (IPM) for hepatitis B virus e antigen (HBeAg) seroconversion in HBeAg-positive chronic hepatitis B (CHB) patients. MethodsThis was a multicenter analysis of 838 patients treated with LAM between January 1999 and August 2004. Of these, 748 patients were followed up for at least 24 months. ResultsThe median age was 43.0 years (range, 19-79 years) and the mean duration of LAM monotherapy was 34.20.7 months. In the multivariate analysis, age (odds ratio [OR]=0.974, P<0.001), baseline alanine aminotransferase level (OR=1.001, P=0.014), and baseline hepatitis B virus DNA level (OR=0.749, P<0.001) were independent factors for HBeAg seroconversion. Based on the predictors, an IPM was established. Patients were classified into high (>50%), intermediate (30-50%), or low (30%) response groups based on their probability of HBeAg seroconversion according to the IPM. The cumulative HBeAg seroconversion rate at 6 years for the high, intermediate, and low response groups was 66.0%, 48.5%, and 21.8%, respectively (P<0.001). ConclusionsAn IPM was developed based on predictors of HBeAg seroconversion in HBeAg-positive CHB patients on LAM monotherapy. This model will allow screening of LAM responders prior to the commencement of antiviral treatment.
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