Predictors of response to infliximab in luminal Crohn's disease

被引:33
作者
Laharie, D [1 ]
Salzmann, M
Boubekeur, H
Richy, F
Amouretti, M
Quinton, A
Couzigou, P
Lamouliatte, H
Zerbib, F
机构
[1] Hop Haut Leveque, Serv Hepatogastroenterol, F-33600 Pessac, France
[2] Hop St Andre, Serv Hepatogastroenterol, F-33075 Bordeaux, France
[3] Univ Victor Segalen Bordeaux 2, Bacteriol Lab, F-33076 Bordeaux, France
来源
GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE | 2005年 / 29卷 / 02期
关键词
D O I
10.1016/S0399-8320(05)80718-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aims - To identify predictive factors of response to infliximab in luminal Crohn's disease (CD). Patients and Methods - All consecutive patients with luminal CID treated with infliximab between October 1999 and March 2003 in Bordeaux's referral centers were included. All had at least 3 months follow-up post infliximab infusion and no prior treatment with infliximab. Response rates were determined 2 and 8 weeks after infusion according to Crohn's Disease Activity Index (CDAI) (remission = CDAI < 150 and response = CDAI decrease more than 100). Results - Among 44 patients (33 female; mean age 35 14 yr.), 39 (88 %) had a clinical response 2 weeks after infusion (79 % in remission). At week 8, the rate of response was 61.4 % and exclusive colonic involvement predicted sustained response to treatment (P = 0.03). The probability of remission at 56 weeks was 21.4 %. Multivariate analysis demonstrated that the only factor associated with response duration was initiating immunosuppressive (IS) therapy in women (RR = 3.61 95 %Cl[ 1.25-10.41], P = 0.017). Conclusion - Exclusive colonic involvement is the only predictive factor of sustained response to infliximab in luminal CID. At the time of infliximab infusion, initiation or modification of IS therapy may favor sustained response, at least in women.
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页码:145 / 149
页数:5
相关论文
共 21 条
[1]   The molecular classification of the clinical manifestations of Crohn's disease [J].
Ahmad, T ;
Armuzzi, A ;
Bunce, M ;
Mulcahy-Hawes, K ;
Marshall, SE ;
Orchard, TR ;
Crawshaw, J ;
Large, O ;
De Silva, A ;
Cook, JT ;
Barnardo, M ;
Cullen, S ;
Welsh, KI ;
Jewell, DP .
GASTROENTEROLOGY, 2002, 122 (04) :854-866
[2]   Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease [J].
Baert, F ;
Noman, M ;
Vermeire, S ;
Van Assche, G ;
D'Haens, G ;
Carbonez, A ;
Rutgeerts, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :601-608
[3]  
BERNADES P, 1978, GASTROEN CLIN BIOL, V2, P1047
[4]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[5]   The safety profile of infliximab in patients with Crohn's disease: The Mayo Clinic experience in 500 patients [J].
Colombel, JF ;
Loftus, EV ;
Tremaine, WJ ;
Egan, LJ ;
Harmsen, WS ;
Schleck, CD ;
Zinsmeister, AR ;
Sandborn, WJ .
GASTROENTEROLOGY, 2004, 126 (01) :19-31
[6]   Long-term evolution of disease behavior of Crohn's disease [J].
Cosnes, J ;
Cattan, S ;
Blain, A ;
Beaugerie, L ;
Carbonnel, F ;
Parc, R ;
Gendre, JP .
INFLAMMATORY BOWEL DISEASES, 2002, 8 (04) :244-250
[7]  
Doubremelle M, 2002, GASTROEN CLIN BIOL, V26, P973
[8]   A simple classification of Crohn's disease: Report of the Working Party for the world congresses of gastroenterology, Vienna 1998 [J].
Gasche, C ;
Scholmerich, J ;
Brynskov, J ;
D'Haens, G ;
Hanauer, SB ;
Irvine, EJ ;
Jewell, DP ;
Rachmilewitz, D ;
Sachar, DB ;
Sandborn, WJ ;
Sutherland, LR .
INFLAMMATORY BOWEL DISEASES, 2000, 6 (01) :8-15
[9]   Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial [J].
Hanauer, SB ;
Feagan, BG ;
Lichtenstein, GR ;
Mayer, LF ;
Schreiber, S ;
Colombel, JF ;
Rachmilewitz, D ;
Wolf, DC ;
Olson, A ;
Bao, WH ;
Rutgeerts, P .
LANCET, 2002, 359 (9317) :1541-1549
[10]   Response to infliximab is related to disease duration in paediatric Crohn's disease [J].
Lionetti, P ;
Bronzini, F ;
Salvestrini, C ;
Bascietto, C ;
Canani, RB ;
Dé Angelis, GL ;
Guariso, G ;
Martelossi, S ;
Papadatou, B ;
Barabino, A .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 18 (04) :425-431