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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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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 |
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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 |
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