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Mortality in patients with chronic hepatitis B treated with tenofovir or entecavir: A multinational study

Authors
Jang, Tyng-YuanLiang, Po-ChengJun, Dae WonJung, Jang HanToyoda, HidenoriWang, Chih-WenYuen, Man-FungCheung, Ka ShingYoon, Eileen L.An, JihyunYasuda, SatoshiKim, Sung EunEnomoto, MasaruKozuka, RitsuzoChuma, MakotoNozaki, AkitoIshikawa, ToruWatanabe, TsunamasaAtsukawa, MasanoriArai, TaeangHayama, KorenobuIshigami, MasatoshiCho, Yong KyunOgawa, EiichiKim, Hyoung SuShim, Jae-JunUojima, HarukiJeong, Soung WonAhn, Sang BongTakaguchi, KoichiSenoh, TomonoriButi, MariaElena, Vargas-Accarino iAbe, HiroshiTakahashi, HirokazuInoue, KaoriYeh, Ming-LunDai, Chia-YenHuang, Jee-FuHuang, Chung-FengChuang, Wan-LongNguyen, Mindie H.Yu, Ming-Lung
Issue Date
Jun-2024
Publisher
Blackwell Publishing Inc.
Keywords
antigen; antiviral; cohort; ETV; fibrosis; hepatocellular carcinoma; liver; NA; prognosis; TDF
Citation
Journal of Gastroenterology and Hepatology, v.39, no.6, pp 1190 - 1197
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
Journal of Gastroenterology and Hepatology
Volume
39
Number
6
Start Page
1190
End Page
1197
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/195233
DOI
10.1111/jgh.16537
ISSN
0815-9319
1440-1746
Abstract
Background and Aim: The benefits of entecavir (ETV) versus tenofovir disoproxil fumarate (TDF) in reducing the development of chronic hepatitis B (CHB)-related hepatocellular carcinoma remain controversial. Whether mortality rates differ between patients with CHB treated with ETV and those treated with TDF is unclear. Methods: A total of 2542 patients with CHB treated with either ETV or TDF were recruited from a multinational cohort. A 1:1 propensity score matching was performed to balance the differences in baseline characteristics between the two patient groups. We aimed to compare the all-cause, liver-related, and non-liver-related mortality between patients receiving ETV and those receiving TDF. Results: The annual incidence of all-cause mortality in the entire cohort was 1.0/100 person-years (follow-up, 15 757.5 person-years). Patients who received TDF were younger and had a higher body mass index, platelet count, hepatitis B virus deoxyribonucleic acid levels, and proportion of hepatitis B e-antigen seropositivity than those who received ETV. The factors associated with all-cause mortality were fibrosis-4 index > 6.5 (hazard ratio [HR]/confidence interval [CI]: 3.13/2.15-4.54, P < 0.001), age per year increase (HR/CI: 1.05/1.04-1.07, P < 0.001), alanine aminotransferase level per U/L increase (HR/CI: 0.997/0.996-0.999, P = 0.003), and gamma-glutamyl transferase level per U/L increase (HR/CI: 1.002/1.001-1.003, P < 0.001). No significant difference in all-cause mortality was observed between the ETV and TDF groups (log-rank test, P = 0.69). After propensity score matching, no significant differences in all-cause, liver-related, or non-liver-related mortality were observed between the two groups. Conclusions: Long-term outcomes of all-cause mortality and liver-related and non-liver-related mortality did not differ between patients treated with ETV and those receiving TDF.
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