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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
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.
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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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