Reinforced interferon alpha-2b and ribavirin is more effective than standard combination therapy in the retreatment of chronic hepatitis C previously nonresponsive to interferon: a randomized trial

被引:13
作者
Poynard, T
Marcellin, P
Bissery, A
Myers, RP
Moussalli, J
Degos, F
Dhumeaux, D
Riachi, G
Bronowicki, JP
Brissot, P
Buffet, C
Serfaty, L
Naveau, S
Sogni, P
Beaugrand, M
Gayno, S
Larrey, D
Samuel, D
Eugene, C
Pol, S
Bedossa, P
Daurat, V
Chaumet-Riffaud, P
机构
[1] Univ Paris 06, Grp Hosp Pitie Salpetriere, Serv Hepatogastroenterol, CNRS,ESA 8067, F-75651 Paris 13, France
[2] Hop Beaujon, Clichy, France
[3] Hop Henri Mondor, Cretoil, France
[4] Hop Charles Nicolle, Rouen, France
[5] Hop Brabois, Nancy, France
[6] Hop Pontchaillou, Rennes, France
[7] Hop Bicetre, Le Kremlin Bicetre, France
[8] Hop St Antoine, F-75571 Paris, France
[9] Hop Antoine Beclere, Clamart, France
[10] Hop Cochin, F-75674 Paris, France
[11] Hop Jean Verdier, Bondy, France
[12] Hop Rene Dubos, Pontoise, France
[13] Hop St Eloi, Montpellier, France
[14] Hop Paul Brousse, Villejuif, France
[15] Hop St Louis, Delegat Rech Clin, Paris, France
关键词
adverse events; HCV; interferon; nonresponder; ribavirin;
D O I
10.1046/j.1365-2893.2003.00427.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Interferon-alpha (IFN) monotherapy results in sustained virological clearance in a minority of patients with chronic hepatitis C. The aim of this study was to assess the effect of a reinforced regimen combining ribavirin and high-dose IFN for 48 weeks compared with a nonreinforced regimen combining a standard IFN regimen and ribavirin for 24 weeks in nonresponders with chronic hepatitis C. A total of 231 patients with chronic hepatitis C and previous nonresponse to IFN monotherapy were randomized. The reinforced group (n = 114) received IFN-2b 6 million units (MU) thrice weekly (TIW) and ribavirin for 48 weeks, and the nonreinforced group (n = 117) received IFN-2b 3 MU TIW and ribavirin for 24 weeks. The main outcome measure was a sustained virological response, defined as negative serum hepatitis C virus (HCV)-RNA 24 weeks following the end of treatment. This endpoint was determined in 98 patients of the reinforced group and 105 patients of the nonreinforced group. At the end of follow-up, a sustained virological response was observed in 29 of the 98 patients (29.6%) in the reinforced group vs 16 of the 105 patients (15.2%) in the nonreinforced group (P = 0.014). In multivariate analysis, factors associated with a sustained virological response were treated with a reinforced regimen [odds ratio (OR) 2.9; P = 0.06] and genotype 2 or 3 (OR 8.8; P < 0.0002). A total of 160 patients had paired biopsies before and after treatment. Histological activity improvement was observed in 32 of 80 patients (40%) and fibrosis worsening in 26 of 80 patients (33%) in the reinforced group vs 13 of 80 (16%) and 19 of 80 (24%) in the nonreinforced group (P = 0.30 and 0.20, respectively). Hence in nonresponders, a high-dose 48-week regimen of IFN and ribavirin combination was more effective than a regimen with interferon at lower dose and ribavirin for 24 weeks only.
引用
收藏
页码:197 / 204
页数:8
相关论文
共 26 条
[1]  
ALBERTI A, 1997, HEPATOLOGY S1, V26, pA137
[2]  
[Anonymous], HEPATOLOGY 1
[3]   An algorithm for the grading of activity in chronic hepatitis C [J].
Bedossa, P ;
Poynard, T .
HEPATOLOGY, 1996, 24 (02) :289-293
[4]   High-dose interferon-alpha(2b) for re-treatment of nonresponders or relapsing patients with chronic hepatitis C - A controlled randomized trial [J].
Bonkovsky, HL ;
Clifford, BD ;
Smith, LJ ;
Allan, C ;
Banner, B .
DIGESTIVE DISEASES AND SCIENCES, 1996, 41 (01) :149-154
[5]   Interferon and ribavirin for patients with chronic hepatitis C who did not respond to previous interferon therapy: A meta-analysis of controlled and uncontrolled trials [J].
Cheng, SJ ;
Bonis, PAL ;
Lau, J ;
Pham, NQ ;
Wong, JB .
HEPATOLOGY, 2001, 33 (01) :231-240
[6]   Interferon and ribavirin vs interferon alone in the re-treatment of chronic hepatitis C previously nonresponsive to interferon - A meta-analysis of randomized trials [J].
Cummings, KJ ;
Lee, SM ;
West, ES ;
Cid-Ruzafa, J ;
Fein, SG ;
Aoki, Y ;
Sulkowski, MS ;
Goodman, SN .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (02) :193-199
[7]   High-dose prolonged combination therapy in non-responders to interferon monotherapy for chronic hepatitis C [J].
Di Marco, V ;
Vaccaro, A ;
Ferraro, D ;
Alaimo, G ;
Rodolico, V ;
Parisi, P ;
Peralta, S ;
Di Stefano, R ;
Almasio, PL ;
Craxì, A .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (07) :953-958
[8]   Pegylated (40 kDa) interferon alfa-2a (PEGASYS®) in combination with ribavirin:: Efficacy and safety results from a phase III, randomized, actively-controlled, multicenter study [J].
Fried, MW ;
Shiffman, ML ;
Reddy, RK ;
Smith, C ;
Marino, G ;
Goncales, F ;
Haeussinger, D ;
Diago, M ;
Carosi, G ;
Zarski, JP ;
Hoffman, J ;
Yu, J .
GASTROENTEROLOGY, 2001, 120 (05) :A55-A55
[9]   Human leucocyte interferon-alpha in chronic hepatitis C resistant to recombinant or lymphoblastoid interferon-alpha: A randomized controlled trial [J].
Gaeta, GB ;
DiVirgilio, D ;
Russo, G ;
Stornaiuolo, G ;
Nicolella, U ;
Colella, F ;
Grimaldi, M ;
Pasquale, G ;
Giusti, G .
JOURNAL OF VIRAL HEPATITIS, 1997, 4 (03) :209-214
[10]   SUICIDE ASSOCIATED WITH ALFA-INTERFERON THERAPY FOR CHRONIC VIRAL-HEPATITIS [J].
JANSSEN, HLA ;
BROUWER, JT ;
VANDERMAST, RC ;
SCHALM, SW .
JOURNAL OF HEPATOLOGY, 1994, 21 (02) :241-243