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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
Author(s) -
Suzuki Fumitaka,
Akuta Norio,
Suzuki Yoshiyuki,
Sezaki Hitomi,
Yatsuji Hiromi,
Kawamura Yusuke,
Hosaka Tetsuya,
Kobayashi Masahiro,
Arase Yasuji,
Ikeda Kenji,
Mineta Rie,
Iwasaki Satomi,
Watahiki Sachiyo,
Kobayashi Mariko,
Miyakawa Yuzo,
Kumada Hiromitsu
Publication year - 2009
Publication title -
hepatology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.123
H-Index - 75
eISSN - 1872-034X
pISSN - 1386-6346
DOI - 10.1111/j.1872-034x.2009.00548.x
Subject(s) - ribavirin , telaprevir , medicine , pegylated interferon , hepatitis c virus , gastroenterology , interferon , hepatitis c , viral load , virology , virus , immunology
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 The treatment was withdrawn in seven (35%) patients, mostly due to reduced hemoglobin of less than 8.5 g/dL, of whom six (86%) remained clear of HCV RNA at 12 weeks.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.