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Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development

Nowadays, patients with chronic hepatitis C in all countries are generally treated with interferon (IFN), and more than 50% of patients become HCV-RNA negative following PEG-IFN plus ribavirin therapy, but unfortunately, the IFN therapy is not effective in about 70% of patients with HCV-associated L...

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Autores principales: Rino, Yasushi, Tarao, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195877/
https://www.ncbi.nlm.nih.gov/pubmed/22084728
http://dx.doi.org/10.5402/2011/390676
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author Rino, Yasushi
Tarao, Kazuo
author_facet Rino, Yasushi
Tarao, Kazuo
author_sort Rino, Yasushi
collection PubMed
description Nowadays, patients with chronic hepatitis C in all countries are generally treated with interferon (IFN), and more than 50% of patients become HCV-RNA negative following PEG-IFN plus ribavirin therapy, but unfortunately, the IFN therapy is not effective in about 70% of patients with HCV-associated LC. In Japan, HCC actually develops in about 7% of those patients every year. A strategy for preventing HCC development other than IFN therapy is, therefore, urgently needed for those patients. We reported that the recurrence rate and the development of HCC was more rapid in the high serum ALT level (>80 IU) patients with HCV-associated LC. Sho-saiko-to, Juzen-taiho-to, and stronger-neo minophagen C are herbal medicines used in Japan to treat chronic viral liver diseases, and they work by reducing inflammatory processes and controlling ALT levels. Aggressive reduction therapy for ALT levels in HCV-LC patients could significantly prevent HCC development.
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spelling pubmed-31958772011-11-14 Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development Rino, Yasushi Tarao, Kazuo ISRN Oncol Review Article Nowadays, patients with chronic hepatitis C in all countries are generally treated with interferon (IFN), and more than 50% of patients become HCV-RNA negative following PEG-IFN plus ribavirin therapy, but unfortunately, the IFN therapy is not effective in about 70% of patients with HCV-associated LC. In Japan, HCC actually develops in about 7% of those patients every year. A strategy for preventing HCC development other than IFN therapy is, therefore, urgently needed for those patients. We reported that the recurrence rate and the development of HCC was more rapid in the high serum ALT level (>80 IU) patients with HCV-associated LC. Sho-saiko-to, Juzen-taiho-to, and stronger-neo minophagen C are herbal medicines used in Japan to treat chronic viral liver diseases, and they work by reducing inflammatory processes and controlling ALT levels. Aggressive reduction therapy for ALT levels in HCV-LC patients could significantly prevent HCC development. International Scholarly Research Network 2011 2011-07-07 /pmc/articles/PMC3195877/ /pubmed/22084728 http://dx.doi.org/10.5402/2011/390676 Text en Copyright © 2011 Y. Rino and K. Tarao. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Rino, Yasushi
Tarao, Kazuo
Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development
title Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development
title_full Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development
title_fullStr Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development
title_full_unstemmed Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development
title_short Anti-Inflammatory Drugs Reduce the Risk of Hepatocellular Carcinoma Development
title_sort anti-inflammatory drugs reduce the risk of hepatocellular carcinoma development
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195877/
https://www.ncbi.nlm.nih.gov/pubmed/22084728
http://dx.doi.org/10.5402/2011/390676
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