Combined treatment with pegylated interferon (α-2b) and ribavirin in the acute phase of hepatitis C virus recurrence after liver transplantation

被引:112
|
作者
Castells, L
Vargas, V
Allende, H
Bilbao, I
Lázaro, JL
Margarit, C
Esteban, R
Guardia, J
机构
[1] Univ Autonoma Barcelona, Hosp Gen Valle Hebron, Dept Internal Med, Liver Unit, Barcelona 08035, Spain
[2] Univ Autonoma Barcelona, Hosp Gen Valle Hebron, Dept Pathol Anat, E-08193 Barcelona, Spain
[3] Univ Autonoma Barcelona, Hosp Gen Valle Hebron, Liver Transplantat Unit, E-08193 Barcelona, Spain
关键词
hepatitis C virus; antiviral therapy; acute HCV reinfection; post-liver transplantation;
D O I
10.1016/j.jhep.2005.02.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The efficacy and safety of treatment with pegylated interferon alpha-2b (Peg-Intron,(TM) 1.5 ug/kg) and ribavirin (400-800 mg) in the acute phase of recurrent HCV after LT is presented. Methods: Twenty-four patients (17 men) transplanted for HCV-associated cirrhosis (genotype 1b) were treated for at least 6 months and compared with 24 consecutive transplant patients (16 men) without antiviral therapy (controls). Results: At completion of treatment, 14/24 treated patients (58%) achieved HCV-RNA negativity, compared to none of controls (P < 0.0001). Sustained virological response (SVR) occurred in 8/23 treated patients (34.7%) who reached week 24 after treatment and none of controls (P < 0.005). At 12 weeks after treatment, 15/24 patients (62.5%) had an early virological response (EVR) (seven tested HCV-RNA negative). SVR was associated with absence of corticosteroid bolus administration (P=0.01), presence of EVR (P=0.002) and absence of cytomegalovirus infection (P=0.001). Haematological adverse effects included anaemia, 17/24 cases (71%) and leukopenia, 23/24 cases (96%). One patient presented mild acute rejection that resolved by adjusting immunosuppressive dose. Conclusions: Treatment with pegylated interferon alpha-2b plus ribavirin in the acute phase of HCV reinfection yielded an EVR of 62.5% and a SVR of 34.7%. The combination was safe, with a low rate of therapy withdrawal. (c) 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 59
页数:7
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