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Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma
Metabolic‐associated fatty liver disease (MAFLD) is a major cause of liver‐related complications, including hepatocellular carcinoma (HCC). While MAFLD‐related HCC is known to occur in the absence of cirrhosis, our understanding of MAFLD‐related HCC in this setting is limited. Here, we characterize...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789832/ https://www.ncbi.nlm.nih.gov/pubmed/33437906 http://dx.doi.org/10.1002/hep4.1606 |
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author | Chen, Vincent L. Yeh, Ming‐Lun Yang, Ju Dong Leong, Jennifer Huang, Daniel Q. Toyoda, Hidenori Chen, Yao‐Li Guy, Jennifer Maeda, Mayumi Tsai, Pei‐Chien Huang, Chung‐Feng Yasuda, Satoshi Le, An K. Dang, Hansen Giama, Nasra H. Ali, Hamdi A. Zhang, Ning Wang, Xiaozhong Jun, Dae Won Tseng, Cheng‐Hao Hsu, Yao‐Chun Huang, Jee‐Fu Dai, Chia‐Yen Chuang, Wan‐Long Zhu, Qiang Dan, Yock Young Schwartz, Myron Roberts, Lewis R. Yu, Ming‐Lung Nguyen, Mindie H. |
author_facet | Chen, Vincent L. Yeh, Ming‐Lun Yang, Ju Dong Leong, Jennifer Huang, Daniel Q. Toyoda, Hidenori Chen, Yao‐Li Guy, Jennifer Maeda, Mayumi Tsai, Pei‐Chien Huang, Chung‐Feng Yasuda, Satoshi Le, An K. Dang, Hansen Giama, Nasra H. Ali, Hamdi A. Zhang, Ning Wang, Xiaozhong Jun, Dae Won Tseng, Cheng‐Hao Hsu, Yao‐Chun Huang, Jee‐Fu Dai, Chia‐Yen Chuang, Wan‐Long Zhu, Qiang Dan, Yock Young Schwartz, Myron Roberts, Lewis R. Yu, Ming‐Lung Nguyen, Mindie H. |
author_sort | Chen, Vincent L. |
collection | PubMed |
description | Metabolic‐associated fatty liver disease (MAFLD) is a major cause of liver‐related complications, including hepatocellular carcinoma (HCC). While MAFLD‐related HCC is known to occur in the absence of cirrhosis, our understanding of MAFLD‐related HCC in this setting is limited. Here, we characterize MAFLD‐related HCC and the impact of cirrhosis and screening on survival. This was a multicenter, retrospective, cohort study of MAFLD‐related HCC. MAFLD was defined based on the presence of race‐adjusted overweight, diabetes, or both hypertension and dyslipidemia in the absence of excess alcohol use or other underlying cause of liver disease. The primary outcome of interest was overall survival, and the primary dependent variables were cirrhosis status and prior HCC screening. We used Kaplan‐Meier methods to estimate overall survival and Cox proportional hazards models and random forest machine learning to determine factors associated with prognosis. This study included 1,382 patients from 11 centers in the United States and East/Southeast Asia. Cirrhosis was present in 62% of patients, but under half of these patients had undergone imaging within 12 months of HCC diagnosis. Patients with cirrhosis were more likely to have early stage disease but less often received curative therapy. After adjustment, cirrhosis was not associated with prognosis, but the presence of cancer‐related symptoms at diagnosis was associated with poorer prognosis. Conclusion: Cirrhosis was not associated with overall survival in this cohort of MAFLD‐related HCC, while diagnosis in the presence of symptoms was associated with poorer prognosis. The HCC surveillance rate in patients with MAFLD‐related HCC was disappointingly low in a multicenter cohort. |
format | Online Article Text |
id | pubmed-7789832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77898322021-01-11 Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma Chen, Vincent L. Yeh, Ming‐Lun Yang, Ju Dong Leong, Jennifer Huang, Daniel Q. Toyoda, Hidenori Chen, Yao‐Li Guy, Jennifer Maeda, Mayumi Tsai, Pei‐Chien Huang, Chung‐Feng Yasuda, Satoshi Le, An K. Dang, Hansen Giama, Nasra H. Ali, Hamdi A. Zhang, Ning Wang, Xiaozhong Jun, Dae Won Tseng, Cheng‐Hao Hsu, Yao‐Chun Huang, Jee‐Fu Dai, Chia‐Yen Chuang, Wan‐Long Zhu, Qiang Dan, Yock Young Schwartz, Myron Roberts, Lewis R. Yu, Ming‐Lung Nguyen, Mindie H. Hepatol Commun Original Articles Metabolic‐associated fatty liver disease (MAFLD) is a major cause of liver‐related complications, including hepatocellular carcinoma (HCC). While MAFLD‐related HCC is known to occur in the absence of cirrhosis, our understanding of MAFLD‐related HCC in this setting is limited. Here, we characterize MAFLD‐related HCC and the impact of cirrhosis and screening on survival. This was a multicenter, retrospective, cohort study of MAFLD‐related HCC. MAFLD was defined based on the presence of race‐adjusted overweight, diabetes, or both hypertension and dyslipidemia in the absence of excess alcohol use or other underlying cause of liver disease. The primary outcome of interest was overall survival, and the primary dependent variables were cirrhosis status and prior HCC screening. We used Kaplan‐Meier methods to estimate overall survival and Cox proportional hazards models and random forest machine learning to determine factors associated with prognosis. This study included 1,382 patients from 11 centers in the United States and East/Southeast Asia. Cirrhosis was present in 62% of patients, but under half of these patients had undergone imaging within 12 months of HCC diagnosis. Patients with cirrhosis were more likely to have early stage disease but less often received curative therapy. After adjustment, cirrhosis was not associated with prognosis, but the presence of cancer‐related symptoms at diagnosis was associated with poorer prognosis. Conclusion: Cirrhosis was not associated with overall survival in this cohort of MAFLD‐related HCC, while diagnosis in the presence of symptoms was associated with poorer prognosis. The HCC surveillance rate in patients with MAFLD‐related HCC was disappointingly low in a multicenter cohort. John Wiley and Sons Inc. 2020-09-24 /pmc/articles/PMC7789832/ /pubmed/33437906 http://dx.doi.org/10.1002/hep4.1606 Text en © 2020 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of the American Association for the Study of Liver Diseases. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Chen, Vincent L. Yeh, Ming‐Lun Yang, Ju Dong Leong, Jennifer Huang, Daniel Q. Toyoda, Hidenori Chen, Yao‐Li Guy, Jennifer Maeda, Mayumi Tsai, Pei‐Chien Huang, Chung‐Feng Yasuda, Satoshi Le, An K. Dang, Hansen Giama, Nasra H. Ali, Hamdi A. Zhang, Ning Wang, Xiaozhong Jun, Dae Won Tseng, Cheng‐Hao Hsu, Yao‐Chun Huang, Jee‐Fu Dai, Chia‐Yen Chuang, Wan‐Long Zhu, Qiang Dan, Yock Young Schwartz, Myron Roberts, Lewis R. Yu, Ming‐Lung Nguyen, Mindie H. Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma |
title | Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma |
title_full | Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma |
title_fullStr | Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma |
title_full_unstemmed | Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma |
title_short | Effects of Cirrhosis and Diagnosis Scenario in Metabolic‐Associated Fatty Liver Disease‐Related Hepatocellular Carcinoma |
title_sort | effects of cirrhosis and diagnosis scenario in metabolic‐associated fatty liver disease‐related hepatocellular carcinoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789832/ https://www.ncbi.nlm.nih.gov/pubmed/33437906 http://dx.doi.org/10.1002/hep4.1606 |
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