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Evolution of Interferon-Based Therapy for Chronic Hepatitis C
Since 1986, interferon-alfa (IFN-α) monotherapy has been administered for patients with chronic hepatitis C (CHC). However, sustained response rate is only about 8% to 9%. Subsequent introduction of ribavirin in combination with IFN-α was a major breakthrough in the treatment of CHC. Sustained virol...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990099/ https://www.ncbi.nlm.nih.gov/pubmed/21152178 http://dx.doi.org/10.1155/2010/140953 |
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author | Chen, Chun-Hao Yu, Ming-Lung |
author_facet | Chen, Chun-Hao Yu, Ming-Lung |
author_sort | Chen, Chun-Hao |
collection | PubMed |
description | Since 1986, interferon-alfa (IFN-α) monotherapy has been administered for patients with chronic hepatitis C (CHC). However, sustained response rate is only about 8% to 9%. Subsequent introduction of ribavirin in combination with IFN-α was a major breakthrough in the treatment of CHC. Sustained virological responses (SVRs) rate is about 30% in hepatitis C virus genotype 1 (HCV-1) patients, and is about 65% in HCV-2 or -3 patients. After 2000, pegylated interferon (PegIFN) much improved the rates of SVR. Presently, PegIFN-α-ribavirin combination therapy has been current standard of care for patients infected with HCV. In patients with HCV-1, treatment for 48 weeks is optimal, but 24 weeks of treatment is sufficient in HCV-2 or -3 infected patients. Clinical factors have been identified as predictors for the efficacy of the IFN-based therapy. The baseline factor most strongly predictive of an SVR is the presence of HCV-2 or -3 infections. Rapid virological response (RVR) is the single best predictor of an SVR to PegIFN-ribavirin therapy. If patients can't achieve a RVR but achieve a complete early virological response (cEVR), treatment with current standard of care can provide more than 90% SVR rate. HCV-1 patients who do not achieve an EVR should discontinue the therapy. Recent advances of protease inhibitor may contribute the development of a novel triple combination therapy. |
format | Text |
id | pubmed-2990099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-29900992010-12-09 Evolution of Interferon-Based Therapy for Chronic Hepatitis C Chen, Chun-Hao Yu, Ming-Lung Hepat Res Treat Review Article Since 1986, interferon-alfa (IFN-α) monotherapy has been administered for patients with chronic hepatitis C (CHC). However, sustained response rate is only about 8% to 9%. Subsequent introduction of ribavirin in combination with IFN-α was a major breakthrough in the treatment of CHC. Sustained virological responses (SVRs) rate is about 30% in hepatitis C virus genotype 1 (HCV-1) patients, and is about 65% in HCV-2 or -3 patients. After 2000, pegylated interferon (PegIFN) much improved the rates of SVR. Presently, PegIFN-α-ribavirin combination therapy has been current standard of care for patients infected with HCV. In patients with HCV-1, treatment for 48 weeks is optimal, but 24 weeks of treatment is sufficient in HCV-2 or -3 infected patients. Clinical factors have been identified as predictors for the efficacy of the IFN-based therapy. The baseline factor most strongly predictive of an SVR is the presence of HCV-2 or -3 infections. Rapid virological response (RVR) is the single best predictor of an SVR to PegIFN-ribavirin therapy. If patients can't achieve a RVR but achieve a complete early virological response (cEVR), treatment with current standard of care can provide more than 90% SVR rate. HCV-1 patients who do not achieve an EVR should discontinue the therapy. Recent advances of protease inhibitor may contribute the development of a novel triple combination therapy. Hindawi Publishing Corporation 2010 2010-10-10 /pmc/articles/PMC2990099/ /pubmed/21152178 http://dx.doi.org/10.1155/2010/140953 Text en Copyright © 2010 C.-H. Chen and M.-L. Yu. 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 Chen, Chun-Hao Yu, Ming-Lung Evolution of Interferon-Based Therapy for Chronic Hepatitis C |
title | Evolution of Interferon-Based Therapy for Chronic Hepatitis C |
title_full | Evolution of Interferon-Based Therapy for Chronic Hepatitis C |
title_fullStr | Evolution of Interferon-Based Therapy for Chronic Hepatitis C |
title_full_unstemmed | Evolution of Interferon-Based Therapy for Chronic Hepatitis C |
title_short | Evolution of Interferon-Based Therapy for Chronic Hepatitis C |
title_sort | evolution of interferon-based therapy for chronic hepatitis c |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990099/ https://www.ncbi.nlm.nih.gov/pubmed/21152178 http://dx.doi.org/10.1155/2010/140953 |
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