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The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study

BACKGROUND: Beta-blockers can reduce recurrence, metastasis, and mortality in various cancers. In this study, we investigated the effect of propranolol, a non-selective beta-blocker on overall survival (OS) in unresectable/metastatic hepatocellular carcinoma (HCC) and on recurrence-free survival (RF...

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Autores principales: Chang, Ping-Ying, Chung, Chi-Hsiang, Chang, Wei-Chou, Lin, Chun-Shu, Lin, Hsuan-Hwai, Dai, Ming-Shen, Ho, Ching-Liang, Chien, Wu-Chien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534323/
https://www.ncbi.nlm.nih.gov/pubmed/31125347
http://dx.doi.org/10.1371/journal.pone.0216828
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author Chang, Ping-Ying
Chung, Chi-Hsiang
Chang, Wei-Chou
Lin, Chun-Shu
Lin, Hsuan-Hwai
Dai, Ming-Shen
Ho, Ching-Liang
Chien, Wu-Chien
author_facet Chang, Ping-Ying
Chung, Chi-Hsiang
Chang, Wei-Chou
Lin, Chun-Shu
Lin, Hsuan-Hwai
Dai, Ming-Shen
Ho, Ching-Liang
Chien, Wu-Chien
author_sort Chang, Ping-Ying
collection PubMed
description BACKGROUND: Beta-blockers can reduce recurrence, metastasis, and mortality in various cancers. In this study, we investigated the effect of propranolol, a non-selective beta-blocker on overall survival (OS) in unresectable/metastatic hepatocellular carcinoma (HCC) and on recurrence-free survival (RFS) in resectable, curable HCC. METHODS: Data were retrieved from the Taiwan National Health Insurance Research Database between January 2000 and December 2013. Propranolol users (for >1 year) and non-propranolol users were matched using a 1:2 propensity score in both cohorts. RESULTS: The unresectable/metastatic HCC cohort comprised 1,560 propranolol users and 3,120 non-propranolol users (control group). On multivariate Cox regression analysis of HCC mortality, propranolol significantly reduced the mortality risk by 22% (hazard ratio [HR] = 0.78, 95% confidence interval [CI] 0.72–0.84, P <0.001). On stratified Cox regression analysis, propranolol also reduced the mortality risk in HCC patients with hepatitis B (HR = 0.92, 95% CI 0.85–0.99, P = 0.045), hepatitis C (HR = 0.85, 95% CI = 0.78–0.92, P = 0.001), liver cirrhosis (HR = 0.78, 95% CI = 0.72–0.85, P <0.001), and diabetes mellitus (HR = 0.87, 95% CI = 0.81–0.94, P = 0.008). The resectable, curable HCC cohort comprised 289 propranolol users and 578 non-propranolol users (control group), but there was no significant difference in RFS (P = 0.762) between propranolol and non-propranolol users. CONCLUSION: This study revealed that propranolol could improve OS in unresectable/metastatic HCC.
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spelling pubmed-65343232019-06-05 The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study Chang, Ping-Ying Chung, Chi-Hsiang Chang, Wei-Chou Lin, Chun-Shu Lin, Hsuan-Hwai Dai, Ming-Shen Ho, Ching-Liang Chien, Wu-Chien PLoS One Research Article BACKGROUND: Beta-blockers can reduce recurrence, metastasis, and mortality in various cancers. In this study, we investigated the effect of propranolol, a non-selective beta-blocker on overall survival (OS) in unresectable/metastatic hepatocellular carcinoma (HCC) and on recurrence-free survival (RFS) in resectable, curable HCC. METHODS: Data were retrieved from the Taiwan National Health Insurance Research Database between January 2000 and December 2013. Propranolol users (for >1 year) and non-propranolol users were matched using a 1:2 propensity score in both cohorts. RESULTS: The unresectable/metastatic HCC cohort comprised 1,560 propranolol users and 3,120 non-propranolol users (control group). On multivariate Cox regression analysis of HCC mortality, propranolol significantly reduced the mortality risk by 22% (hazard ratio [HR] = 0.78, 95% confidence interval [CI] 0.72–0.84, P <0.001). On stratified Cox regression analysis, propranolol also reduced the mortality risk in HCC patients with hepatitis B (HR = 0.92, 95% CI 0.85–0.99, P = 0.045), hepatitis C (HR = 0.85, 95% CI = 0.78–0.92, P = 0.001), liver cirrhosis (HR = 0.78, 95% CI = 0.72–0.85, P <0.001), and diabetes mellitus (HR = 0.87, 95% CI = 0.81–0.94, P = 0.008). The resectable, curable HCC cohort comprised 289 propranolol users and 578 non-propranolol users (control group), but there was no significant difference in RFS (P = 0.762) between propranolol and non-propranolol users. CONCLUSION: This study revealed that propranolol could improve OS in unresectable/metastatic HCC. Public Library of Science 2019-05-24 /pmc/articles/PMC6534323/ /pubmed/31125347 http://dx.doi.org/10.1371/journal.pone.0216828 Text en © 2019 Chang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chang, Ping-Ying
Chung, Chi-Hsiang
Chang, Wei-Chou
Lin, Chun-Shu
Lin, Hsuan-Hwai
Dai, Ming-Shen
Ho, Ching-Liang
Chien, Wu-Chien
The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study
title The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study
title_full The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study
title_fullStr The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study
title_full_unstemmed The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study
title_short The effect of propranolol on the prognosis of hepatocellular carcinoma: A nationwide population-based study
title_sort effect of propranolol on the prognosis of hepatocellular carcinoma: a nationwide population-based study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534323/
https://www.ncbi.nlm.nih.gov/pubmed/31125347
http://dx.doi.org/10.1371/journal.pone.0216828
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