Literature DB >> 24162072

Low-dose pegylated interferon-α2a plus ribavirin therapy for elderly and/or cirrhotic patients with HCV genotype-1b and high viral load.

Hideyuki Tamai1, Yoshiyuki Mori, Naoki Shingaki, Akira Kawashima, Hiroshi Tsukuda, Katsuhiko Higashi, Kosaku Moribata, Masanori Kawaguchi, Kazuki Ueda, Hisanobu Deguchi, Izumi Inoue, Takao Maekita, Mikitaka Iguchi, Jun Kato, Masao Ichinose.   

Abstract

BACKGROUND: Pegylated interferon (PEG-IFN) plus ribavirin therapy is still recommended for elderly and/or cirrhotic patients. This study examined whether sustained virological response (SVR) to low-dose PEG-IFN-α2a plus ribavirin therapy for elderly and/or cirrhotic patients could be predicted based on viral reduction within 2 weeks after therapy initiation or interleukin IL-(28B) polymorphism and viral mutations.
METHODS: Participants comprised 115 elderly (≥65 years) and/or cirrhotic patients with genotype-1b and high viral load. Reduced doses of PEG-IFN-α2a (90 μg/kg/week) and ribavirin (400-800 mg/day) were administered for 48-72 weeks based on virological response of each patient.
RESULTS: SVR was achieved in 34% (39/115), and treatment was discontinued in 15% (17/115). Univariate analysis identified age, α-fetoprotein, fibrosis marker, interferon sensitivity-determining region (ISDR), IL-28B polymorphism and level of viral reduction within 2 weeks as factors contributing significantly to SVR. However, no significant differences were noted in core amino acid substitutions. Multivariate analysis identified age, hyaluronic acid, ISDR and viral reduction as factors independently associated with SVR. Positive predictive value (PPV) and negative predictive value (NPV) of SVR based on the level of viral reduction at 2 weeks (cutoff level, 1.7 log IU/ml) were 83% and 84%, respectively. The PPV of SVR based on IL-28B major and ISDR mutant was 70%, and the NPV of SVR based on IL-28B minor and wild-type ISDR was 89%.
CONCLUSIONS: Evaluations of viral reduction at 2 weeks or both IL-28B and ISDR are useful to predict SVR to low-dose PEG-IFN-α2a plus ribavirin therapy for elderly and/or cirrhotic patients.

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Year:  2013        PMID: 24162072     DOI: 10.3851/IMP2696

Source DB:  PubMed          Journal:  Antivir Ther        ISSN: 1359-6535


  4 in total

1.  Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks.

Authors:  Hideyuki Tamai; Ryo Shimizu; Naoki Shingaki; Yoshiyuki Mori; Shuya Maeshima; Junya Nuta; Yoshimasa Maeda; Kosaku Moribata; Yosuke Muraki; Hisanobu Deguchi; Izumi Inoue; Takao Maekita; Mikitaka Iguchi; Jun Kato; Masao Ichinose
Journal:  Hepat Res Treat       Date:  2014-09-28

2.  Simeprevir-Based Triple Therapy with Reduced Doses of Pegylated Interferon α-2a Plus Ribavirin for Interferon Ineligible Patients with Genotype 1b Hepatitis C Virus.

Authors:  Hideyuki Tamai; Yoshiyuki Ida; Akira Kawashima; Naoki Shingaki; Ryo Shimizu; Kosaku Moribata; Tetsushi Nasu; Takao Maekita; Mikitaka Iguchi; Jun Kato; Taisei Nakao; Masayuki Kitano
Journal:  Gut Liver       Date:  2017-07-15       Impact factor: 4.519

3.  The Real-World Safety and Efficacy of Daclatasvir and Asunaprevir for Elderly Patients.

Authors:  Shinya Taki; Hideyuki Tamai; Yoshiyuki Ida; Naoki Shingaki; Akira Kawashima; Ryo Shimizu; Kosaku Moribata; Takao Maekita; Mikitaka Iguchi; Jun Kato; Taisei Nakao; Masayuki Kitano
Journal:  Gut Liver       Date:  2018-01-15       Impact factor: 4.519

4.  Low-Dose Pegylated Interferon α-2b Plus Ribavirin for Elderly and/or Cirrhotic Patients with Genotype 2 Hepatitis C Virus.

Authors:  Hideyuki Tamai; Naoki Shingaki; Yoshiyuki Mori; Kosaku Moribata; Akira Kawashima; Yoshimasa Maeda; Toru Niwa; Hisanobu Deguchi; Izumi Inoue; Takao Maekita; Mikitaka Iguchi; Jun Kato; Masao Ichinose
Journal:  Gut Liver       Date:  2016-07-16       Impact factor: 4.519

  4 in total

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