Safety and anti-HCV effect of prolonged intravenous silibinin in HCV genotype 1 subjects in the immediate liver transplant period

被引:27
作者
Barcena, Rafael [1 ]
Moreno, Ana [1 ]
Angel Rodriguez-Gandia, Miguel [1 ]
Albillos, Agustin [1 ]
Arocena, Carlos [1 ]
Blesa, Carlos [1 ]
Garcia-Hoz, Fernando [1 ]
Graus, Javier [1 ]
Nuno, Javier [1 ]
Lopez-Hervas, Pedro [1 ]
Gajate, Luis [1 ]
Martinez, Adolfo [1 ]
Bermejo, Teresa [1 ]
Luisa Mateos, Maria [1 ]
del Campo, Santos [1 ]
机构
[1] Hosp Ramon & Cajal, Liver Transplant Grp, E-28034 Madrid, Spain
关键词
HCV recurrence; Liver transplantation; Intravenous silibinin; Safety; HCV-RNA kinetics; HEPATITIS-C-VIRUS; ANTIVIRAL THERAPY; PEGYLATED INTERFERON; MONOCLONAL-ANTIBODY; INFECTED PATIENTS; REINFECTION; RECURRENCE; PHASE; NONRESPONDERS; TOLERABILITY;
D O I
10.1016/j.jhep.2012.10.009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background 82 Aims: Reinfection of the graft is the rule in patients with HCV cirrhosis undergoing liver transplantation, and HCV-RNA reaches pre-transplantation levels within the first month. Short-term intravenous silibinin monotherapy is safe and shows a potent in vivo anti-HCV effect. We aimed at evaluating the safety and antiviral effect of prolonged intravenous silibinin, started immediately before liver transplantation. Methods: Single centre, prospective, pilot study, to assess the safety and effect on HCV-RNA kinetics during at least 21 days of intravenous silibinin monotherapy (20 mg/kg/day) in 9 consecutive HCV genotype 1 subjects, in comparison to a control, non-treated group of 7 consecutive prior transplanted subjects under the same immunosuppressive regimen (basiliximab, steroids, delayed tacrolimus, micophenolate). Results: Intravenous silibinin led to significant, maintained and progressive HCV-RNA decreases (mean HCV-RNA drop at week 3, -4.1 +/- 1.3 log(10), IU/ml), and lack of viral breakthrough during administration. Four patients (44%) reached negative HCV-RNA, maintained during silibinin treatment, vs. none in the control group, but HCV-RNA relapsed in all of them after a median of 21 days (16-28), following silibinin withdrawal. Partial responders to silibinin showed marked decreases in HCV-RNA when compared to controls, but lower than complete responders. There were no clinical adverse effects, and silibinin led to asymptomatic transient hyperbilirubinemia (week 2, 4.2 +/- 2.2 vs. 2.5 +/- 3.6 mg/dl; p = 0.02). Conclusions: Prolonged intravenous silibinin monotherapy was safe in the immediate liver transplantation period, leading to a potent and time dependent antiviral effect and lack of HCV-RNA breakthrough during administration. However, HCV-RNA rebounded after withdrawal, and silibinin monotherapy did not avoid reinfection of the graft. Published by Elsevier B.V. on behalf of the European Association for the Study of the Liver.
引用
收藏
页码:421 / 426
页数:6
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