TY - JOUR
T1 - Combined treatment with pegylated interferon (α-2b) and ribavirin in the acute phase of hepatitis C virus recurrence after liver transplantation
AU - Castells, Lluís
AU - Vargas, Víctor
AU - Allende, Helena
AU - Bilbao, Itxarone
AU - Lázaro, José Luis
AU - Margarit, Carlos
AU - Esteban, Rafael
AU - Guardia, Jaime
PY - 2005/7/1
Y1 - 2005/7/1
N2 - Background/Aims: The efficacy and safety of treatment with pegylated interferon α-2b (Peg-Intron,™ 1.5 μg/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 α-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. © 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
AB - Background/Aims: The efficacy and safety of treatment with pegylated interferon α-2b (Peg-Intron,™ 1.5 μg/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 α-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. © 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
KW - Acute HCV reinfection
KW - Antiviral therapy
KW - Hepatitis C virus
KW - Post-liver transplantation
U2 - 10.1016/j.jhep.2005.02.015
DO - 10.1016/j.jhep.2005.02.015
M3 - Article
SN - 0168-8278
VL - 43
SP - 53
EP - 59
JO - Journal of Hepatology
JF - Journal of Hepatology
ER -