Telaprevir-based triple therapy for hepatitis C null responders among living donor liver transplant recipients

被引:5
|
作者
Kaneko, Junichi [1 ]
Sugawara, Yasuhiko [1 ]
Yamaguchi, Takamune [1 ]
Harada, Nobuhiro [1 ]
Akamatsu, Nobuhisa [1 ]
Ishizawa, Takeaki [1 ]
Aoki, Taku [1 ]
Sakamoto, Yoshihiro [1 ]
Hasegawa, Kiyoshi [1 ]
Tamura, Sumihito [1 ]
Tanaka, Tomohiro [2 ]
Kokudo, Norihiro [1 ]
机构
[1] Univ Tokyo, Dept Surg, Div Artificial Organ & Transplantat, Tokyo 1138655, Japan
[2] Univ Tokyo, Organ Transplantat Serv, Tokyo 1138655, Japan
基金
日本学术振兴会;
关键词
Hepatitis C; Telaprevir; living donor liver transplantation; Japanese; null responder; GENOTYPE; 1; TREATMENT-NAIVE; RIBAVIRIN; VIRUS; CYCLOSPORINE; INTERFERON; EXPERIENCE; EFFICACY; SAFETY;
D O I
10.5582/bst.2014.01101
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:339 / 345
页数:7
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