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Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies
Hepatitis C virus (HCV) is known to cause chronic hepatitis C, and its sequelae of cirrhosis and hepatocellular carcinoma. Hepatitis C genotype 3 (HCV-3) in particular is notorious for causing accelerated liver fibrosis, cardiovascular, and metabolic effects, thus increasing morbidity and mortality....
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578556/ https://www.ncbi.nlm.nih.gov/pubmed/29201722 http://dx.doi.org/10.5005/jp-journals-10018-1163 |
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author | Saeed, Naba Gurakar, Ahmet |
author_facet | Saeed, Naba Gurakar, Ahmet |
author_sort | Saeed, Naba |
collection | PubMed |
description | Hepatitis C virus (HCV) is known to cause chronic hepatitis C, and its sequelae of cirrhosis and hepatocellular carcinoma. Hepatitis C genotype 3 (HCV-3) in particular is notorious for causing accelerated liver fibrosis, cardiovascular, and metabolic effects, thus increasing morbidity and mortality. It is the commonest variant in Asian countries like India and Pakistan. It is also one of the hardest-to-treat genotypes, especially among treatment-experienced and cirrhotic patients. Due to limited health care affordability and accessibility in these areas, many patients remain untreated. Until recently, the established therapy for HCV had been a combination of pegylated interferon + ribavirin. However, it was only effective in about half of patients and had severe adverse effects; hence a more efficacious option needed to be found. Recent advances have led to the development of sofosbuvir, an NS5B inhibitor that is fast becoming the standard of care, in combination with other novel drugs. It was initially marketed at $1,000 per pill, a cost that was too high for most. Thus, it has not been utilized as a global therapy as yet. Formulation of effective interferon-free regimens is a huge milestone, and awareness needs to be raised regarding these new highly effective options in both the physician and the patient population. This article discusses the newest drugs and combinations that have been developed in the fight against HCV-3, as a treatment outline for HCV-3-dominant areas. It also highlights recent breakthroughs in cost reductions of these drugs and the effort to make them globally accessible. HOW TO CITE THIS ARTICLE: Saeed N, Gurakar A. Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies. Euroasian J Hepato-Gastroenterol 2016;6(1):35-42. |
format | Online Article Text |
id | pubmed-5578556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-55785562017-11-30 Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies Saeed, Naba Gurakar, Ahmet Euroasian J Hepatogastroenterol Review Article Hepatitis C virus (HCV) is known to cause chronic hepatitis C, and its sequelae of cirrhosis and hepatocellular carcinoma. Hepatitis C genotype 3 (HCV-3) in particular is notorious for causing accelerated liver fibrosis, cardiovascular, and metabolic effects, thus increasing morbidity and mortality. It is the commonest variant in Asian countries like India and Pakistan. It is also one of the hardest-to-treat genotypes, especially among treatment-experienced and cirrhotic patients. Due to limited health care affordability and accessibility in these areas, many patients remain untreated. Until recently, the established therapy for HCV had been a combination of pegylated interferon + ribavirin. However, it was only effective in about half of patients and had severe adverse effects; hence a more efficacious option needed to be found. Recent advances have led to the development of sofosbuvir, an NS5B inhibitor that is fast becoming the standard of care, in combination with other novel drugs. It was initially marketed at $1,000 per pill, a cost that was too high for most. Thus, it has not been utilized as a global therapy as yet. Formulation of effective interferon-free regimens is a huge milestone, and awareness needs to be raised regarding these new highly effective options in both the physician and the patient population. This article discusses the newest drugs and combinations that have been developed in the fight against HCV-3, as a treatment outline for HCV-3-dominant areas. It also highlights recent breakthroughs in cost reductions of these drugs and the effort to make them globally accessible. HOW TO CITE THIS ARTICLE: Saeed N, Gurakar A. Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies. Euroasian J Hepato-Gastroenterol 2016;6(1):35-42. Jaypee Brothers Medical Publishers 2016 2016-07-09 /pmc/articles/PMC5578556/ /pubmed/29201722 http://dx.doi.org/10.5005/jp-journals-10018-1163 Text en Copyright © 2016; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Review Article Saeed, Naba Gurakar, Ahmet Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies |
title | Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies |
title_full | Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies |
title_fullStr | Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies |
title_full_unstemmed | Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies |
title_short | Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies |
title_sort | tackling hcv-3 in asia: breakthroughs for efficient and cost-effective treatment strategies |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578556/ https://www.ncbi.nlm.nih.gov/pubmed/29201722 http://dx.doi.org/10.5005/jp-journals-10018-1163 |
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