| Literature DB >> 25641181 |
Junichi Kaneko1, Yasuhiko Sugawara, Takamune Yamaguchi, Nobuhiro Harada, Nobuhisa Akamatsu, Takeaki Ishizawa, Taku Aoki, Yoshihiro Sakamoto, Kiyoshi Hasegawa, Sumihito Tamura, Tomohiro Tanaka, Norihiro Kokudo.
Abstract
Telaprevir (TVR), a direct -acting protease inhibitor, was recently reported to improve treatment efficacy when used in combination with peg-interferon (PEG-IFN) and ribavirin (RBV) as triple therapy for HCV in non-transplant patients. The aim of the present study was to investigate the feasibility of TVR-based triple therapy among Japanese living donor liver transplant (LDLT) recipients who had been resistant to dual treatment with PEG-IFN and RBV. Among 133 HCV-positive LDLT recipients, 8 null responders during or after dual treatment with PEG-IFN and RBV were finally indicated for TVR-based triple therapy after treatment. All 8 patients had been resistant to dual treatment with PEG-IFN and RBV. While the cyclosporine trough level was well controlled with an 80% dose reduction during TVR administration, the end - of - treatment response rate was only 25% (2/8), with 63% (5/8) of patients developing anemia that required a blood transfusion and 50% (4/8) of patients developing leukopenia that required filgrastim. Dose reduction or treatment discontinuation was required in all cases. Based on the poor efficacy and the unacceptable high rate of cytopenic events, TVR-based triple therapy is not indicated for those resistant to dual treatment with PEG-IFN and RBV.Entities:
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Year: 2014 PMID: 25641181 DOI: 10.5582/bst.2014.01101
Source DB: PubMed Journal: Biosci Trends ISSN: 1881-7815 Impact factor: 2.400