Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success

Currently, hepatitis C virus (HCV) antiviral therapy is characterized by long duration, a multitude of side effects, difficult administration and suboptimal success; clearly, alternatives are needed. Collectively, specifically targeted antiviral therapy for HCV (STAT-C) molecules achieve rapid viral...

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Main Author: Curtis L Cooper
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Canadian Journal of Gastroenterology
Online Access:http://dx.doi.org/10.1155/2010/125435
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author Curtis L Cooper
author_facet Curtis L Cooper
author_sort Curtis L Cooper
collection DOAJ
description Currently, hepatitis C virus (HCV) antiviral therapy is characterized by long duration, a multitude of side effects, difficult administration and suboptimal success; clearly, alternatives are needed. Collectively, specifically targeted antiviral therapy for HCV (STAT-C) molecules achieve rapid viral suppression and very high rapid virological response rates, and improve sustained virological response rates. The attrition rate of agents within this class has been high due to various toxicities. Regardless, several STAT-C molecules are poised to become the standard of care for HCV treatment in the foreseeable future. Optimism must be tempered with concerns related to the rapid development of drug resistance with resulting HCV rebound. Strategies including induction dosing with interferon and ribavirin, use of combination high-potency STAT-C molecules and an intensive emphasis on adherence to HCV antiviral therapy will be critical to the success of this promising advance in HCV therapy.
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spelling doaj-art-040428e829ee4d99b06f2bc88a3f9f8f2025-02-03T05:54:07ZengWileyCanadian Journal of Gastroenterology0835-79002010-01-0124638539010.1155/2010/125435Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment SuccessCurtis L Cooper0Ottawa Hospital and University of Ottawa, Ottawa, Ontario, CanadaCurrently, hepatitis C virus (HCV) antiviral therapy is characterized by long duration, a multitude of side effects, difficult administration and suboptimal success; clearly, alternatives are needed. Collectively, specifically targeted antiviral therapy for HCV (STAT-C) molecules achieve rapid viral suppression and very high rapid virological response rates, and improve sustained virological response rates. The attrition rate of agents within this class has been high due to various toxicities. Regardless, several STAT-C molecules are poised to become the standard of care for HCV treatment in the foreseeable future. Optimism must be tempered with concerns related to the rapid development of drug resistance with resulting HCV rebound. Strategies including induction dosing with interferon and ribavirin, use of combination high-potency STAT-C molecules and an intensive emphasis on adherence to HCV antiviral therapy will be critical to the success of this promising advance in HCV therapy.http://dx.doi.org/10.1155/2010/125435
spellingShingle Curtis L Cooper
Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success
Canadian Journal of Gastroenterology
title Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success
title_full Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success
title_fullStr Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success
title_full_unstemmed Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success
title_short Viral Response to Specifically Targeted Antiviral Therapy for Hepatitis C and the Implications for Treatment Success
title_sort viral response to specifically targeted antiviral therapy for hepatitis c and the implications for treatment success
url http://dx.doi.org/10.1155/2010/125435
work_keys_str_mv AT curtislcooper viralresponsetospecificallytargetedantiviraltherapyforhepatitiscandtheimplicationsfortreatmentsuccess