Multicenter randomized study comparing initial daily induction with high dose lymphoblastoid interferon vs. standard interferon treatment for chronic hepatitis C

被引:4
作者
Diago, M
Suárez, D
García-Villarreal, L
Castro, A
Domínguez, A
Pardo, M
del Olmo, JA
Pérez-Hernández, F
Aguilar, J
Quiroga, JA
Carreño, V
机构
[1] Fdn Estudio Hepatitis Virales, Madrid 28015, Spain
[2] Hosp Gen Univ, Valencia, Spain
[3] Complejo Hosp Arquitecto Marcide, Ferrol, Spain
[4] Complejo Hosp Materno Insular, Las Palmas Gran Canaria, Spain
[5] Hosp Juan Canalejo, La Coruna, Spain
[6] Hosp Gen Juan Ramon Jimenez, Huelva, Spain
[7] Hosp Pardo de Aravaca, Inst Hepatol, Madrid, Spain
[8] Hosp Clin Univ, Valencia, Spain
[9] Hosp Nuestra Senora Candelaria, Santa Cruz De Tenerife, Spain
[10] Hosp Virgen Rocio, Seville, Spain
关键词
chronic hepatitis C virus (HCV) infection; natural (lymphoblastoid) interferon-alpha; (IFN alpha-n1) therapeutic use; high-dose induction;
D O I
10.1002/jmv.1072
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
One hundred fifty-five chronic hepatitis C patients were assigned at random to receive natural lymphoblastoid interferon (IFN)alpha -n1, s.c., for 13 months in one of three treatment regimens: initial daily induction with 10 million units (MU) followed (group 1, n = 50) or not (group 2, n = 52) by 1 month of rest and then three times weekly 10 MU (2 months), 5 MU (2 months), and 3 MU (8 months); group 3 (n = 53) received tiw 5 MU (2 months) followed by 3 MU (11 months). By intention-to-treat analysis, ALT normalization at completion of treatment was greater in patients who received continuous IFN alpha -n1 therapy with initial daily induction (group 2: 24/52, 46%) compared with those given intermittent therapy with initial daily induction (group 1: 17/50, 34%) and those who received standard IFN alpha -n1 therapy (group 3, 18/53, 34%; P not significant). The sustained ALT response was 26%, 27% and 21% and the sustained virological response was 20%, 27%, and 19%, in groups 1, 2, and 3, respectively. A trend was observed towards a high er biochemical and virological end-of-treatment response in patients given induction therapy (17%) compared with standard therapy (6%, P = 0.053). Sustained biochemical and virological responses were 20%, 27%, and 17% in groups 1, 2, and 3, respectively. Platelet and leukocyte counts decreased following daily high-dose treatment a nd remained low until therapy cessation (P < 0.001). The data suggest that daily s.c. induction with 10 MU IFN<alpha>-n1 followed by intermittent or continuous maintenance therapy for 1 year does not improve the results achieved with the standard 1-year IFN alpha course in the treatment of chronic hepatitis C patients. J. Med. Virol. 64:460-465, 2001. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:460 / 465
页数:6
相关论文
共 25 条
[1]   Natural history of hepatitis C [J].
Alberti, A ;
Chemello, L ;
Benvegnù, L .
JOURNAL OF HEPATOLOGY, 1999, 31 :17-24
[2]  
[Anonymous], 1999, J Hepatol, V30, P956
[3]  
BENHAMOU JP, 1995, J HEPATOL, V21, pA173
[4]  
Cammà C, 1999, AM J GASTROENTEROL, V94, P581, DOI 10.1111/j.1572-0241.1999.00919.x
[5]   TREATMENT OF CHRONIC HEPATITIS-C BY CONTINUOUS SUBCUTANEOUS INFUSION OF INTERFERON-ALPHA [J].
CARRENO, V ;
TAPIA, L ;
RYFF, JC ;
QUIROGA, JA ;
CASTILLO, I .
JOURNAL OF MEDICAL VIROLOGY, 1992, 37 (03) :215-219
[6]  
Colombatto P, 1997, ITAL J GASTROENTEROL, V29, P441
[7]   Reinforced regimen of interferon alfa-2a reduces the incidence of cirrhosis in patients with chronic hepatitis C: a multicentre randomised trial [J].
Degos, F ;
Daurat, V ;
Chevret, S ;
Gayno, S ;
Bastie, A ;
Riachi, G ;
Batolomei-Portal, I ;
Barange, K ;
Moussalli, J ;
Naveau, S ;
Bailly, F ;
Chaumet-Riffaud, P ;
Chastang, C .
JOURNAL OF HEPATOLOGY, 1998, 29 (02) :224-232
[8]  
DESMET VJ, 1994, HEPATOLOGY, V19, P1513, DOI 10.1002/hep.1840190629
[9]   Therapy of hepatitis C: Interferon alfa-n1 trials [J].
Farrell, GC .
HEPATOLOGY, 1997, 26 (03) :S96-S100
[10]   Virological, biochemical and histological effects of human lymphoblastoid interferon in Swedish patients with chronic hepatitis C [J].
Garson, JA ;
Uhnoo, I ;
Whitby, K ;
Braconier, JH ;
Deaville, R ;
Duberg, A ;
Wallmark, E ;
Wistrom, J ;
Goldin, RD ;
Spacey, B .
JOURNAL OF VIRAL HEPATITIS, 1997, 4 (05) :325-331