Sofosbuvir and Daclatasvir Combination Therapy in a Liver Transplant Recipient With Severe Recurrent Cholestatic Hepatitis C

被引:133
作者
Fontana, R. J. [1 ]
Hughes, E. A. [2 ]
Bifano, M. [2 ]
Appelman, H. [3 ]
Dimitrova, D. [2 ]
Hindes, R. [4 ]
Symonds, W. T. [4 ]
机构
[1] Univ Michigan, Med Ctr, Dept Internal Med, Princeton, NJ USA
[2] Bristol Myers Squibb Co, Princeton, NJ USA
[3] Univ Michigan, Med Ctr, Dept Pathol, Princeton, NJ USA
[4] Gilead Sci Inc, Foster City, CA 94404 USA
关键词
Calcineurin inhibitors; direct-acting antiviral agents; hepatitis C; polymerase inhibitors; ANTIVIRAL THERAPY; INFECTION; CYCLOSPORINE; INTERFERON; TACROLIMUS; RIBAVIRIN; GRAFT;
D O I
10.1111/ajt.12209
中图分类号
R61 [外科手术学];
学科分类号
摘要
Recurrent HCV infection following liver transplantation can lead to accelerated allograft injury that is difficult to treat with interferon. The aim of this study is to describe the first ever use of an interferon-free, all oral regimen in a liver transplant recipient with severe recurrent HCV. A 54-year-old male with HCV genotype 1b developed severe cholestatic HCV at 6 months posttransplant with ascites, AST 503IU/mL, alkaline phosphatase of 298IU/mL, HCV RNA of 12000000IU/mL, and histological cholestasis with pericellular fibrosis. Sofosbuvir, an HCV polymerase inhibitor (400mg/day), and daclatasvir, an HCV NS5A replication complex inhibitor (60mg/day), were co-administered for 24 weeks. Within 4 weeks of initiating treatment, serum HCV RNA levels became undetectable and liver biochemistries normalized with concomitant resolution of ascites. The patient achieved a sustained virological response with undetectable HCV RNA at 9 months posttreatment. During and following treatment, the daily dose and blood level of tacrolimus remained stable and unchanged. The rapid and sustained suppression of HCV replication in this liver transplant recipient provides great promise for the use of combination oral antiviral regimens in other immunosuppressed and interferon refractory HCV patients.
引用
收藏
页码:1601 / 1605
页数:5
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