Volume 39, Issue 11 pp. 1056-1063

Rapid loss of hepatitis C virus genotype 1b from serum in patients receiving a triple treatment with telaprevir (MP-424), pegylated interferon and ribavirin for 12 weeks

Fumitaka Suzuki

Corresponding Author

Fumitaka Suzuki

Department of Hepatology and

Dr Fumitaka Suzuki, Department of Hepatology, Toranomon Hospital, 1-3-1, Kajigaya, Takatsu-ku, Kawasaki City 213-8587, Japan. Email: [email protected]Search for more papers by this author
Norio Akuta

Norio Akuta

Department of Hepatology and

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Yoshiyuki Suzuki

Yoshiyuki Suzuki

Department of Hepatology and

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Hitomi Sezaki

Hitomi Sezaki

Department of Hepatology and

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Hiromi Yatsuji

Hiromi Yatsuji

Department of Hepatology and

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Yusuke Kawamura

Yusuke Kawamura

Department of Hepatology and

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Tetsuya Hosaka

Tetsuya Hosaka

Department of Hepatology and

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Masahiro Kobayashi

Masahiro Kobayashi

Department of Hepatology and

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Yasuji Arase

Yasuji Arase

Department of Hepatology and

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Kenji Ikeda

Kenji Ikeda

Department of Hepatology and

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Rie Mineta

Rie Mineta

Research Institute for Hepatology, Toranomon Hospital, Kawasaki City, and

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Satomi Iwasaki

Satomi Iwasaki

Research Institute for Hepatology, Toranomon Hospital, Kawasaki City, and

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Sachiyo Watahiki

Sachiyo Watahiki

Research Institute for Hepatology, Toranomon Hospital, Kawasaki City, and

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Mariko Kobayashi

Mariko Kobayashi

Research Institute for Hepatology, Toranomon Hospital, Kawasaki City, and

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Yuzo Miyakawa

Yuzo Miyakawa

Miyakawa Memorial Research Foundation, Tokyo, Japan

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Hiromitsu Kumada

Hiromitsu Kumada

Department of Hepatology and

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First published: 29 October 2009
Citations: 23

Abstract

Aim: To evaluate the efficacy and safety of the triple treatment with telaprevir (MP-424), pegylated interferon (PEG-IFN) and ribavirin during 12 weeks on-treatment.

Methods: The triple treatment was given to 20 patients with chronic hepatitis C who had been infected with hepatitis C virus (HCV)-1b in high viral load (median: 6.8 log IU/mL [range: 5.5–7.2]), with a median age of 54 years (range: 36–65 years). They were followed for early dynamics of HCV RNA in serum during 12 weeks and side-effects.

Results: HCV RNA levels decreased by 4.8 logs by 7 days and 5.5 logs by 14 days. HCV RNA disappeared in 50% (10/20) at 2 weeks, 79% (15/19) at 4 weeks, 88% (14/16) at 6 weeks, 94% (15/16) at 8 weeks and 100% (13/13) at 12 weeks. HCV RNA disappeared equally frequently in 10 treatment-naive patients, six non-responders to IFN monotherapy and four non-responders to PEG-IFN and ribavirin. It was no different in the patients with and without amino acid substitutions reducing the response to IFN. The treatment was withdrawn in seven (35%) patients, mostly due to reduced hemoglobin of less than 8.5 g/dL, of whom six (86%) remained clear of HCV RNA at 12 weeks.

Conclusion: HCV RNA was lost from serum rapidly and universally in patients infected with HCV-1b in high viral loads by the triple treatment. Because an early loss of HCV RNA correlates with high rates of sustained virological response (SVR), it would increase SVR substantially, and merit the patients who have not responded to previous therapies.

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