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Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients

Statins are associated with a reduced risk of hepatocellular carcinoma (HCC) and have the potential to be an adjuvant agent for HCC. In this study, we examined whether statin use is associated with additional benefits among patients who received curative treatments (CTs) such as surgery, percutaneou...

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Autores principales: Wu, Li-Li, Hsieh, Mao-Chih, Chow, Jyh-Ming, Liu, Shing-Hwa, Chang, Chia-Lun, Wu, Szu-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023877/
https://www.ncbi.nlm.nih.gov/pubmed/27603355
http://dx.doi.org/10.1097/MD.0000000000004639
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author Wu, Li-Li
Hsieh, Mao-Chih
Chow, Jyh-Ming
Liu, Shing-Hwa
Chang, Chia-Lun
Wu, Szu-Yuan
author_facet Wu, Li-Li
Hsieh, Mao-Chih
Chow, Jyh-Ming
Liu, Shing-Hwa
Chang, Chia-Lun
Wu, Szu-Yuan
author_sort Wu, Li-Li
collection PubMed
description Statins are associated with a reduced risk of hepatocellular carcinoma (HCC) and have the potential to be an adjuvant agent for HCC. In this study, we examined whether statin use is associated with additional benefits among patients who received curative treatments (CTs) such as surgery, percutaneous ethanol injection (PEI), and radiofrequency ablation (RFA). We conducted a cohort study using the Taiwan National Health Insurance Research Data linked to the Taiwan Cancer Registry in 2001 to 2012. The patient cohort consisted of those who received different treatments, and we compared patients who received statins with those who did not. Statin users were defined as patients who received >28 cumulative defined daily doses after their HCC diagnosis. We used a time-dependent Cox proportional method to model the time from the HCC diagnosis to any death and HCC death between men who received statins and those who did not after adjusting for confounders. Data on statin prescriptions were collected every 6 months to define the user status. In total, 18,892 patients were included, and the mean follow-up duration was 1.74 years. The adjusted hazard ratio (aHR) of all-cause deaths increased in HCC patients who received RFA/PEI compared to those who received surgery (P < 0.0001 and P < 0.05, with aHRs of 1.81 and 1.16, respectively, for hepatitis B virus [HBV] or non-HBV HCC). However, with the addition of statin use to RFA or PEI, the overall survival was statistically equal. Surgical resection is still superior over other therapies. If HCC patients cannot meet the criteria for surgery, the addition of statin use to RFA or PEI might improve HCC survival.
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spelling pubmed-50238772016-09-26 Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients Wu, Li-Li Hsieh, Mao-Chih Chow, Jyh-Ming Liu, Shing-Hwa Chang, Chia-Lun Wu, Szu-Yuan Medicine (Baltimore) 5700 Statins are associated with a reduced risk of hepatocellular carcinoma (HCC) and have the potential to be an adjuvant agent for HCC. In this study, we examined whether statin use is associated with additional benefits among patients who received curative treatments (CTs) such as surgery, percutaneous ethanol injection (PEI), and radiofrequency ablation (RFA). We conducted a cohort study using the Taiwan National Health Insurance Research Data linked to the Taiwan Cancer Registry in 2001 to 2012. The patient cohort consisted of those who received different treatments, and we compared patients who received statins with those who did not. Statin users were defined as patients who received >28 cumulative defined daily doses after their HCC diagnosis. We used a time-dependent Cox proportional method to model the time from the HCC diagnosis to any death and HCC death between men who received statins and those who did not after adjusting for confounders. Data on statin prescriptions were collected every 6 months to define the user status. In total, 18,892 patients were included, and the mean follow-up duration was 1.74 years. The adjusted hazard ratio (aHR) of all-cause deaths increased in HCC patients who received RFA/PEI compared to those who received surgery (P < 0.0001 and P < 0.05, with aHRs of 1.81 and 1.16, respectively, for hepatitis B virus [HBV] or non-HBV HCC). However, with the addition of statin use to RFA or PEI, the overall survival was statistically equal. Surgical resection is still superior over other therapies. If HCC patients cannot meet the criteria for surgery, the addition of statin use to RFA or PEI might improve HCC survival. Wolters Kluwer Health 2016-09-09 /pmc/articles/PMC5023877/ /pubmed/27603355 http://dx.doi.org/10.1097/MD.0000000000004639 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 5700
Wu, Li-Li
Hsieh, Mao-Chih
Chow, Jyh-Ming
Liu, Shing-Hwa
Chang, Chia-Lun
Wu, Szu-Yuan
Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
title Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
title_full Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
title_fullStr Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
title_full_unstemmed Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
title_short Statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
title_sort statins improve outcomes of nonsurgical curative treatments in hepatocellular carcinoma patients
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023877/
https://www.ncbi.nlm.nih.gov/pubmed/27603355
http://dx.doi.org/10.1097/MD.0000000000004639
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