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Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma

BACKGROUND: There have been few studies on the impact of viral etiology on the prognosis in patients with hepatocellular carcinoma (HCC). The aim of this study was to evaluate the clinical characteristics and survival of patients with viral hepatitis-associated HCC (V-HCC), compared to patients with...

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Autores principales: Alkhalili, Eyas, Greenbaum, Alissa, Luo, Li, Rodriguez, Rodrigo, Caldwell, Katharine, Estrada, Oscar Munoz, O’Neill, Jacqueline, Nir, Itzhak, Morris, Katherine T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hellenic Society of Gastroenterology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198233/
https://www.ncbi.nlm.nih.gov/pubmed/28042245
http://dx.doi.org/10.20524/aog.2016.0097
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author Alkhalili, Eyas
Greenbaum, Alissa
Luo, Li
Rodriguez, Rodrigo
Caldwell, Katharine
Estrada, Oscar Munoz
O’Neill, Jacqueline
Nir, Itzhak
Morris, Katherine T.
author_facet Alkhalili, Eyas
Greenbaum, Alissa
Luo, Li
Rodriguez, Rodrigo
Caldwell, Katharine
Estrada, Oscar Munoz
O’Neill, Jacqueline
Nir, Itzhak
Morris, Katherine T.
author_sort Alkhalili, Eyas
collection PubMed
description BACKGROUND: There have been few studies on the impact of viral etiology on the prognosis in patients with hepatocellular carcinoma (HCC). The aim of this study was to evaluate the clinical characteristics and survival of patients with viral hepatitis-associated HCC (V-HCC), compared to patients with HCC of non-hepatitis B, non-hepatitis C (NBNC-HCC) etiology. METHODS: We performed a retrospective analysis of all patients with HCC treated at our comprehensive cancer center from 2000 through 2014. Patients were divided into two groups according to their viral hepatitis status. Presentation patterns, treatments, and survival data were analyzed. RESULTS: We evaluated 366 patients: 233 patients (63.7%) had V-HCC while 133 (36.3%) patients had NBNC-HCC. V-HCC patients were younger (P<0.0001) and more likely to be male (P=0.001). Decompensated cirrhosis was more prevalent in V-HCC patients (P=0.01). There was no difference in the resectability rate or disease stage. In patients with resectable disease, those with V-HCC were less likely to undergo hepatectomy (23.7% vs. 38%; P=0.04) for more advanced liver disease. The estimated median survival for V-HCC was 13 months compared to 16 months in NBNC-HCC patients (P=0.57). On multivariate analysis, disease stage (P<0.0001) and Child-Pugh class (P<0.0001) were independent factors affecting survival, but viral status was not (P=0.75). CONCLUSION: Despite presenting with more advanced cirrhosis and being less likely to undergo surgery, V-HCC patients had similar survival to patients with NBNC-HCC.
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spelling pubmed-51982332017-01-01 Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma Alkhalili, Eyas Greenbaum, Alissa Luo, Li Rodriguez, Rodrigo Caldwell, Katharine Estrada, Oscar Munoz O’Neill, Jacqueline Nir, Itzhak Morris, Katherine T. Ann Gastroenterol Original Article BACKGROUND: There have been few studies on the impact of viral etiology on the prognosis in patients with hepatocellular carcinoma (HCC). The aim of this study was to evaluate the clinical characteristics and survival of patients with viral hepatitis-associated HCC (V-HCC), compared to patients with HCC of non-hepatitis B, non-hepatitis C (NBNC-HCC) etiology. METHODS: We performed a retrospective analysis of all patients with HCC treated at our comprehensive cancer center from 2000 through 2014. Patients were divided into two groups according to their viral hepatitis status. Presentation patterns, treatments, and survival data were analyzed. RESULTS: We evaluated 366 patients: 233 patients (63.7%) had V-HCC while 133 (36.3%) patients had NBNC-HCC. V-HCC patients were younger (P<0.0001) and more likely to be male (P=0.001). Decompensated cirrhosis was more prevalent in V-HCC patients (P=0.01). There was no difference in the resectability rate or disease stage. In patients with resectable disease, those with V-HCC were less likely to undergo hepatectomy (23.7% vs. 38%; P=0.04) for more advanced liver disease. The estimated median survival for V-HCC was 13 months compared to 16 months in NBNC-HCC patients (P=0.57). On multivariate analysis, disease stage (P<0.0001) and Child-Pugh class (P<0.0001) were independent factors affecting survival, but viral status was not (P=0.75). CONCLUSION: Despite presenting with more advanced cirrhosis and being less likely to undergo surgery, V-HCC patients had similar survival to patients with NBNC-HCC. Hellenic Society of Gastroenterology 2017 2016-10-20 /pmc/articles/PMC5198233/ /pubmed/28042245 http://dx.doi.org/10.20524/aog.2016.0097 Text en Copyright: © Hellenic Society of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Alkhalili, Eyas
Greenbaum, Alissa
Luo, Li
Rodriguez, Rodrigo
Caldwell, Katharine
Estrada, Oscar Munoz
O’Neill, Jacqueline
Nir, Itzhak
Morris, Katherine T.
Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
title Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
title_full Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
title_fullStr Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
title_full_unstemmed Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
title_short Viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
title_sort viral hepatitis status does not affect survival in patients with hepatocellular carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198233/
https://www.ncbi.nlm.nih.gov/pubmed/28042245
http://dx.doi.org/10.20524/aog.2016.0097
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