Cargando…

Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B

It remains controversial whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) is associated with different clinical outcomes for chronic hepatitis B (CHB). This study aimed to compare the long-term risk of ETV versus TDF on hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinom...

Descripción completa

Detalles Bibliográficos
Autores principales: Chang, Te-Sheng, Yang, Yao-Hsu, Chen, Wei-Ming, Shen, Chien-Heng, Tung, Shui-Yi, Yen, Chih-Wei, Hsieh, Yung-Yu, Lee, Chuan-Pin, Tsai, Meng-Ling, Hung, Chao-Hung, Lu, Sheng-Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809351/
https://www.ncbi.nlm.nih.gov/pubmed/33446835
http://dx.doi.org/10.1038/s41598-020-80523-7
_version_ 1783637102477443072
author Chang, Te-Sheng
Yang, Yao-Hsu
Chen, Wei-Ming
Shen, Chien-Heng
Tung, Shui-Yi
Yen, Chih-Wei
Hsieh, Yung-Yu
Lee, Chuan-Pin
Tsai, Meng-Ling
Hung, Chao-Hung
Lu, Sheng-Nan
author_facet Chang, Te-Sheng
Yang, Yao-Hsu
Chen, Wei-Ming
Shen, Chien-Heng
Tung, Shui-Yi
Yen, Chih-Wei
Hsieh, Yung-Yu
Lee, Chuan-Pin
Tsai, Meng-Ling
Hung, Chao-Hung
Lu, Sheng-Nan
author_sort Chang, Te-Sheng
collection PubMed
description It remains controversial whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) is associated with different clinical outcomes for chronic hepatitis B (CHB). This study aimed to compare the long-term risk of ETV versus TDF on hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC) in CHB patients from a large multi-institutional database in Taiwan. From 2011 to 2018, a total of 21,222 CHB patients receiving ETV or TDF were screened for eligibility. Patients with coinfection, preexisting cancer and less than 6 months of follow-up were excluded. Finally, 7248 patients (5348 and 1900 in the ETV and TDF groups, respectively) were linked to the National Cancer Registry database for the development of HCC or ICC. Propensity score matching (PSM) (2:1) analysis was used to adjust for baseline differences. The HCC incidence between two groups was not different in the entire population (hazard ratio [HR] 0.82; 95% confidence interval [CI] 0.66–1.02, p = 0.078) and in the PSM population (HR 0.83; 95% CI 0.65–1.06, p = 0.129). Among decompensated cirrhotic patients, a lower risk of HCC was observed in TDF group than in ETV group (HR 0.54; 95% CI 0.30–0.98, p = 0.043, PSM model). There were no differences between ETV and TDF groups in the ICC incidence (HR 1.84; 95% CI 0.54–6.29, p = 0.330 in the entire population and HR 1.04; 95% CI 0.31–3.52, p = 0.954 in the PSM population, respectively). In conclusion, treatment with ETV and TDF showed a comparable long-term risk of HCC and ICC in CHB patients.
format Online
Article
Text
id pubmed-7809351
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-78093512021-01-15 Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B Chang, Te-Sheng Yang, Yao-Hsu Chen, Wei-Ming Shen, Chien-Heng Tung, Shui-Yi Yen, Chih-Wei Hsieh, Yung-Yu Lee, Chuan-Pin Tsai, Meng-Ling Hung, Chao-Hung Lu, Sheng-Nan Sci Rep Article It remains controversial whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) is associated with different clinical outcomes for chronic hepatitis B (CHB). This study aimed to compare the long-term risk of ETV versus TDF on hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC) in CHB patients from a large multi-institutional database in Taiwan. From 2011 to 2018, a total of 21,222 CHB patients receiving ETV or TDF were screened for eligibility. Patients with coinfection, preexisting cancer and less than 6 months of follow-up were excluded. Finally, 7248 patients (5348 and 1900 in the ETV and TDF groups, respectively) were linked to the National Cancer Registry database for the development of HCC or ICC. Propensity score matching (PSM) (2:1) analysis was used to adjust for baseline differences. The HCC incidence between two groups was not different in the entire population (hazard ratio [HR] 0.82; 95% confidence interval [CI] 0.66–1.02, p = 0.078) and in the PSM population (HR 0.83; 95% CI 0.65–1.06, p = 0.129). Among decompensated cirrhotic patients, a lower risk of HCC was observed in TDF group than in ETV group (HR 0.54; 95% CI 0.30–0.98, p = 0.043, PSM model). There were no differences between ETV and TDF groups in the ICC incidence (HR 1.84; 95% CI 0.54–6.29, p = 0.330 in the entire population and HR 1.04; 95% CI 0.31–3.52, p = 0.954 in the PSM population, respectively). In conclusion, treatment with ETV and TDF showed a comparable long-term risk of HCC and ICC in CHB patients. Nature Publishing Group UK 2021-01-14 /pmc/articles/PMC7809351/ /pubmed/33446835 http://dx.doi.org/10.1038/s41598-020-80523-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chang, Te-Sheng
Yang, Yao-Hsu
Chen, Wei-Ming
Shen, Chien-Heng
Tung, Shui-Yi
Yen, Chih-Wei
Hsieh, Yung-Yu
Lee, Chuan-Pin
Tsai, Meng-Ling
Hung, Chao-Hung
Lu, Sheng-Nan
Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B
title Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B
title_full Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B
title_fullStr Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B
title_full_unstemmed Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B
title_short Long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis B
title_sort long-term risk of primary liver cancers in entecavir versus tenofovir treatment for chronic hepatitis b
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809351/
https://www.ncbi.nlm.nih.gov/pubmed/33446835
http://dx.doi.org/10.1038/s41598-020-80523-7
work_keys_str_mv AT changtesheng longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT yangyaohsu longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT chenweiming longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT shenchienheng longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT tungshuiyi longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT yenchihwei longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT hsiehyungyu longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT leechuanpin longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT tsaimengling longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT hungchaohung longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb
AT lushengnan longtermriskofprimarylivercancersinentecavirversustenofovirtreatmentforchronichepatitisb