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Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma

BACKGROUND/AIMS: Non-alcoholic liver disease and alcoholic liver disease begin as simple steatosis that may progress to steatohepatitis and ensuing liver-related complications such as cirrhosis and hepatocellular carcinoma (HCC). We explored differences in characteristics between non-alcoholic steat...

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Autores principales: Kumar, Rahul, Goh, Boon-Bee George, Kam, Jia-Wen, Chang, Pik-Eu, Tan, Chee-Kiat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association for the Study of the Liver 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160352/
https://www.ncbi.nlm.nih.gov/pubmed/31914720
http://dx.doi.org/10.3350/cmh.2019.0012
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author Kumar, Rahul
Goh, Boon-Bee George
Kam, Jia-Wen
Chang, Pik-Eu
Tan, Chee-Kiat
author_facet Kumar, Rahul
Goh, Boon-Bee George
Kam, Jia-Wen
Chang, Pik-Eu
Tan, Chee-Kiat
author_sort Kumar, Rahul
collection PubMed
description BACKGROUND/AIMS: Non-alcoholic liver disease and alcoholic liver disease begin as simple steatosis that may progress to steatohepatitis and ensuing liver-related complications such as cirrhosis and hepatocellular carcinoma (HCC). We explored differences in characteristics between non-alcoholic steatohepatitis (NASH) and alcoholic steatohepatitis-related (ASH) HCC. METHODS: NASH and ASH patients were identified from our department’s prospective HCC database. A total of 54 and 45 patients met predefined inclusion and exclusion criteria for the NASH-HCC and ASH-HCC groups, respectively. Clinical, biochemical and tumor characteristics were studied. RESULTS: NASH-HCC patients were older compared to ASH-HCC patients (72±9 vs. 66±9 years, P<0.001) and less male predominant (65% vs. 98%, P<0.001). Prevalence of diabetes mellitus (78% vs. 36%, P<0.001) and hypertension (80% vs. 58%, P<0.001) were significantly higher in the NASH-HCC group. Liver function tests and Child-Pugh scores were similar. There were no differences in alpha-fetoprotein level, lesions found at diagnosis (unifocal/multifocal) or prevalence of portal vein invasion. In both groups, almost half of the patients were in TNM stage 4 at the time of diagnosis and more than 50% of patients were not suitable for any therapy. Median survival in the NASH-HCC and ASH-HCC groups were 13 and 7 months respectively (P=0.113). CONCLUSIONS: Despite significant differences in demography of the NASH-HCC and ASH-HCC groups, liver and tumor characteristics were comparable. Most patients were diagnosed late and were not amenable to curative or locoregional therapies. Better characterization of patients with NASH and ASH at risk of HCC is necessary to optimize screening, surveillance, and management strategies.
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spelling pubmed-71603522020-04-21 Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma Kumar, Rahul Goh, Boon-Bee George Kam, Jia-Wen Chang, Pik-Eu Tan, Chee-Kiat Clin Mol Hepatol Original Article BACKGROUND/AIMS: Non-alcoholic liver disease and alcoholic liver disease begin as simple steatosis that may progress to steatohepatitis and ensuing liver-related complications such as cirrhosis and hepatocellular carcinoma (HCC). We explored differences in characteristics between non-alcoholic steatohepatitis (NASH) and alcoholic steatohepatitis-related (ASH) HCC. METHODS: NASH and ASH patients were identified from our department’s prospective HCC database. A total of 54 and 45 patients met predefined inclusion and exclusion criteria for the NASH-HCC and ASH-HCC groups, respectively. Clinical, biochemical and tumor characteristics were studied. RESULTS: NASH-HCC patients were older compared to ASH-HCC patients (72±9 vs. 66±9 years, P<0.001) and less male predominant (65% vs. 98%, P<0.001). Prevalence of diabetes mellitus (78% vs. 36%, P<0.001) and hypertension (80% vs. 58%, P<0.001) were significantly higher in the NASH-HCC group. Liver function tests and Child-Pugh scores were similar. There were no differences in alpha-fetoprotein level, lesions found at diagnosis (unifocal/multifocal) or prevalence of portal vein invasion. In both groups, almost half of the patients were in TNM stage 4 at the time of diagnosis and more than 50% of patients were not suitable for any therapy. Median survival in the NASH-HCC and ASH-HCC groups were 13 and 7 months respectively (P=0.113). CONCLUSIONS: Despite significant differences in demography of the NASH-HCC and ASH-HCC groups, liver and tumor characteristics were comparable. Most patients were diagnosed late and were not amenable to curative or locoregional therapies. Better characterization of patients with NASH and ASH at risk of HCC is necessary to optimize screening, surveillance, and management strategies. The Korean Association for the Study of the Liver 2020-04 2020-01-09 /pmc/articles/PMC7160352/ /pubmed/31914720 http://dx.doi.org/10.3350/cmh.2019.0012 Text en Copyright © 2020 by The Korean Association for the Study of the Liver This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kumar, Rahul
Goh, Boon-Bee George
Kam, Jia-Wen
Chang, Pik-Eu
Tan, Chee-Kiat
Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
title Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
title_full Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
title_fullStr Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
title_full_unstemmed Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
title_short Comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
title_sort comparisons between non-alcoholic steatohepatitis and alcohol-related hepatocellular carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160352/
https://www.ncbi.nlm.nih.gov/pubmed/31914720
http://dx.doi.org/10.3350/cmh.2019.0012
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