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Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals
Hepatitis C virus infection is a major cause of hepatocellular carcinoma worldwide. Interferon has been the major antiviral treatment, yielding viral clearance in approximately half of patients. New direct-acting antivirals substantially improved the cure rate to above 90%. However, access to therap...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348895/ https://www.ncbi.nlm.nih.gov/pubmed/28288626 http://dx.doi.org/10.1186/s12916-017-0815-7 |
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author | Baumert, Thomas F. Jühling, Frank Ono, Atsushi Hoshida, Yujin |
author_facet | Baumert, Thomas F. Jühling, Frank Ono, Atsushi Hoshida, Yujin |
author_sort | Baumert, Thomas F. |
collection | PubMed |
description | Hepatitis C virus infection is a major cause of hepatocellular carcinoma worldwide. Interferon has been the major antiviral treatment, yielding viral clearance in approximately half of patients. New direct-acting antivirals substantially improved the cure rate to above 90%. However, access to therapies remains limited due to the high costs and under-diagnosis of infection in specific subpopulations, e.g., baby boomers, inmates, and injection drug users, and therefore, hepatocellular carcinoma incidence is predicted to increase in the next decades even in high-resource countries. Moreover, cancer risk persists even after 10 years of viral cure, and thus a clinical strategy for its monitoring is urgently needed. Several risk-predictive host factors, e.g., advanced liver fibrosis, older age, accompanying metabolic diseases such as diabetes, persisting hepatic inflammation, and elevated alpha-fetoprotein, as well as viral factors, e.g., core protein variants and genotype 3, have been reported. Indeed, a molecular signature in the liver has been associated with cancer risk even after viral cure. Direct-acting antivirals may affect cancer development and recurrence, which needs to be determined in further investigation. |
format | Online Article Text |
id | pubmed-5348895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53488952017-03-14 Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals Baumert, Thomas F. Jühling, Frank Ono, Atsushi Hoshida, Yujin BMC Med Minireview Hepatitis C virus infection is a major cause of hepatocellular carcinoma worldwide. Interferon has been the major antiviral treatment, yielding viral clearance in approximately half of patients. New direct-acting antivirals substantially improved the cure rate to above 90%. However, access to therapies remains limited due to the high costs and under-diagnosis of infection in specific subpopulations, e.g., baby boomers, inmates, and injection drug users, and therefore, hepatocellular carcinoma incidence is predicted to increase in the next decades even in high-resource countries. Moreover, cancer risk persists even after 10 years of viral cure, and thus a clinical strategy for its monitoring is urgently needed. Several risk-predictive host factors, e.g., advanced liver fibrosis, older age, accompanying metabolic diseases such as diabetes, persisting hepatic inflammation, and elevated alpha-fetoprotein, as well as viral factors, e.g., core protein variants and genotype 3, have been reported. Indeed, a molecular signature in the liver has been associated with cancer risk even after viral cure. Direct-acting antivirals may affect cancer development and recurrence, which needs to be determined in further investigation. BioMed Central 2017-03-14 /pmc/articles/PMC5348895/ /pubmed/28288626 http://dx.doi.org/10.1186/s12916-017-0815-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Minireview Baumert, Thomas F. Jühling, Frank Ono, Atsushi Hoshida, Yujin Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals |
title | Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals |
title_full | Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals |
title_fullStr | Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals |
title_full_unstemmed | Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals |
title_short | Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals |
title_sort | hepatitis c-related hepatocellular carcinoma in the era of new generation antivirals |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348895/ https://www.ncbi.nlm.nih.gov/pubmed/28288626 http://dx.doi.org/10.1186/s12916-017-0815-7 |
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