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Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks
The aim of the present study was to predict sustained virological response (SVR) to telaprevir with pegylated interferon (PEG-IFN) and ribavirin using viral response within 2 weeks after therapy initiation. Thirty-six patients with genotype 1 hepatitis C virus (HCV) and high viral load were treated...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195394/ https://www.ncbi.nlm.nih.gov/pubmed/25328696 http://dx.doi.org/10.1155/2014/748935 |
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author | Tamai, Hideyuki Shimizu, Ryo Shingaki, Naoki Mori, Yoshiyuki Maeshima, Shuya Nuta, Junya Maeda, Yoshimasa Moribata, Kosaku Muraki, Yosuke Deguchi, Hisanobu Inoue, Izumi Maekita, Takao Iguchi, Mikitaka Kato, Jun Ichinose, Masao |
author_facet | Tamai, Hideyuki Shimizu, Ryo Shingaki, Naoki Mori, Yoshiyuki Maeshima, Shuya Nuta, Junya Maeda, Yoshimasa Moribata, Kosaku Muraki, Yosuke Deguchi, Hisanobu Inoue, Izumi Maekita, Takao Iguchi, Mikitaka Kato, Jun Ichinose, Masao |
author_sort | Tamai, Hideyuki |
collection | PubMed |
description | The aim of the present study was to predict sustained virological response (SVR) to telaprevir with pegylated interferon (PEG-IFN) and ribavirin using viral response within 2 weeks after therapy initiation. Thirty-six patients with genotype 1 hepatitis C virus (HCV) and high viral load were treated by telaprevir-based triple therapy. SVR was achieved in 72% (26/36) of patients. Significant differences between the SVR group and non-SVR group were noted regarding response to prior PEG-IFN plus ribavirin, interleukin (IL)28B polymorphism, amino acid substitution at core 70, cirrhosis, hyaluronic acid level, and HCV-RNA reduction within 2 weeks. Setting 4.56 logIU/mL as the cut-off value for HCV-RNA reduction at 2 weeks, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for predicting SVR were 77%, 86%, 95%, 50%, and 79%, respectively, and for neither the IL28B minor allele nor core 70 mutant were 80%, 71%, 91%, 50%, and 78%, respectively. In conclusion, evaluation of viral reduction at 2 weeks or the combination of IL28B polymorphism and amino acid substitution at core 70 are useful for predicting SVR to telaprevir with PEG-IFN and ribavirin therapy. |
format | Online Article Text |
id | pubmed-4195394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41953942014-10-19 Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks Tamai, Hideyuki Shimizu, Ryo Shingaki, Naoki Mori, Yoshiyuki Maeshima, Shuya Nuta, Junya Maeda, Yoshimasa Moribata, Kosaku Muraki, Yosuke Deguchi, Hisanobu Inoue, Izumi Maekita, Takao Iguchi, Mikitaka Kato, Jun Ichinose, Masao Hepat Res Treat Clinical Study The aim of the present study was to predict sustained virological response (SVR) to telaprevir with pegylated interferon (PEG-IFN) and ribavirin using viral response within 2 weeks after therapy initiation. Thirty-six patients with genotype 1 hepatitis C virus (HCV) and high viral load were treated by telaprevir-based triple therapy. SVR was achieved in 72% (26/36) of patients. Significant differences between the SVR group and non-SVR group were noted regarding response to prior PEG-IFN plus ribavirin, interleukin (IL)28B polymorphism, amino acid substitution at core 70, cirrhosis, hyaluronic acid level, and HCV-RNA reduction within 2 weeks. Setting 4.56 logIU/mL as the cut-off value for HCV-RNA reduction at 2 weeks, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for predicting SVR were 77%, 86%, 95%, 50%, and 79%, respectively, and for neither the IL28B minor allele nor core 70 mutant were 80%, 71%, 91%, 50%, and 78%, respectively. In conclusion, evaluation of viral reduction at 2 weeks or the combination of IL28B polymorphism and amino acid substitution at core 70 are useful for predicting SVR to telaprevir with PEG-IFN and ribavirin therapy. Hindawi Publishing Corporation 2014 2014-09-28 /pmc/articles/PMC4195394/ /pubmed/25328696 http://dx.doi.org/10.1155/2014/748935 Text en Copyright © 2014 Hideyuki Tamai et al. 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 | Clinical Study Tamai, Hideyuki Shimizu, Ryo Shingaki, Naoki Mori, Yoshiyuki Maeshima, Shuya Nuta, Junya Maeda, Yoshimasa Moribata, Kosaku Muraki, Yosuke Deguchi, Hisanobu Inoue, Izumi Maekita, Takao Iguchi, Mikitaka Kato, Jun Ichinose, Masao Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks |
title | Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks |
title_full | Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks |
title_fullStr | Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks |
title_full_unstemmed | Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks |
title_short | Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks |
title_sort | prediction of sustained virological response to telaprevir-based triple therapy using viral response within 2 weeks |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195394/ https://www.ncbi.nlm.nih.gov/pubmed/25328696 http://dx.doi.org/10.1155/2014/748935 |
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