Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies
- PMID: 29201722
- PMCID: PMC5578556
- DOI: 10.5005/jp-journals-10018-1163
Tackling HCV-3 in Asia: Breakthroughs for Efficient and Cost-effective Treatment Strategies
Abstract
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.
Keywords: Genotype 3; Hepatitis C; New therapies; Sofosbuvir..
Conflict of interest statement
Source of support: Nil Conflict of interest: None
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References
-
- Deinstang JL, McHutchinson JG. American Gastroenterological Association technical review on the management of hepatitis C. Gastroenterology. 2006 Jan;130(1):231–264. - PubMed
-
- World Health Organization. Hepatitis C. Available from: http://www.euro.who. int/en/what-we-do/health-topics/communicable-diseas... .
-
- Simmonds P, Bukh J, Combet C, Deléage G, Enomoto N, Feinstone S, Halfon P, Inchauspé G, Kuiken C, Maertens G et al. Consensus proposals for a unified system of nomenclature of hepatitis C virus genotypes. Hepatology. 2005 Oct;42(4):962–973. - PubMed
-
- Negro F. Steatosis and insulin resistance in response to treatment of chronic hepatitis C. J Viral Hepat. 2012 Jan;19(Suppl 1):42–47. - PubMed
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