Efficacy and tolerance of infliximab in children and adolescents with Crohn's disease

被引:66
作者
Lamireau, T [1 ]
Cézard, JPC [1 ]
Dabadie, A [1 ]
Goulet, O [1 ]
Lachaux, A [1 ]
Turck, D [1 ]
Maurage, C [1 ]
Morali, A [1 ]
Sokal, E [1 ]
Belli, D [1 ]
Stoller, J [1 ]
Cadranel, S [1 ]
Ginies, JL [1 ]
Viola, S [1 ]
Huet, FD [1 ]
Languepin, J [1 ]
Lenaerts, C [1 ]
Bury, F [1 ]
Sarles, J [1 ]
机构
[1] Hop Enfants, Unite Gastroenterol Pediat, F-33077 Bordeaux, France
关键词
Crohn's disease; children; infliximab;
D O I
10.1097/00054725-200411000-00008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Infliximab, a monoclonal antibody against tumor necrosis factor-alpha, has been shown to be effective for the treatment of refractory Crohn's disease in adult patients, but experience in pediatrics is limited. This retrospective study included 88 children and adolescents, 39 girls and 49 boys, with a median age of 14 years (range 3.3-17.9). Infliximab was indicated for active disease (66%) and/or fistulas (42%) that were refractory to corticosteroids (70%), and/or other immunosuppressive (82%) agents, and/or parenteral nutrition (20%). Patients received 1 to 17 infusions (median 4) of 5 mg/kg (range 3.8-7.3) of infliximab during a median time period of 4 months (1-17 months). Infusion reaction was noted in 13 patients (15%), with a total of 16 reactions in 450 infusions (4%). At Day 90 after the first infusion of infliximab, symptoms improved in 49% of patients, whereas 29% of patients were in remission and 13% of patients relapsed. From Day 0 to Day 90, Harvey-Bradshaw score decreased from 7.5 to 2.8 (P < 0.001), C-reactive protein from 36 to 16 mg/L (P < 0.01), and 1-hour erythrocyte sedimentation rate from 35 to 17 mm (P < 0.01). Dosage of corticosteroids decreased from to 0.59 to 0.17 mg/kg/d (P < 0.001); 53% of patients could be weaned of corticosteroids and 92% of parenteral nutrition. Treatment with infliximab is well tolerated and effective in most children and adolescents with Crohn's disease that is refractory to conventional immuno suppressive therapy. Nevertheless, long-term efficacy remains to be shown, and further studies are urgently needed to precisely determine the best modality of continuing treatment.
引用
收藏
页码:745 / 750
页数:6
相关论文
共 36 条
[1]
Growth suppression by glucocorticoid therapy [J].
Allen, DB .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1996, 25 (03) :699-&
[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]
Infliximab (REMICADE) therapy in the treatment of pediatric Crohn's disease [J].
Baldassano, R ;
Braegger, CP ;
Escher, JC ;
DeWoody, K ;
Hendricks, DF ;
Keenan, GF ;
Winter, HS .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (04) :833-838
[4]
Response of fistulating Crohn's disease to infliximab treatment assessed by magnetic resonance imaging [J].
Bell, SJ ;
Halligan, S ;
Windsor, ACJ ;
Williams, AB ;
Wiesel, P ;
Kamm, MA .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (03) :387-393
[5]
TUMOR-NECROSIS-FACTOR-ALPHA IN STOOL AS A MARKER OF INTESTINAL INFLAMMATION [J].
BRAEGGER, CP ;
NICHOLLS, S ;
MURCH, SH ;
STEPHENS, S ;
MACDONALD, TT .
LANCET, 1992, 339 (8785) :89-91
[6]
TUMOR-NECROSIS-FACTOR ALPHA-PRODUCING CELLS IN THE INTESTINAL-MUCOSA OF CHILDREN WITH INFLAMMATORY BOWEL-DISEASE [J].
BREESE, EJ ;
MICHIE, CA ;
NICHOLLS, SW ;
MURCH, SH ;
WILLIAMS, CB ;
DOMIZIO, P ;
WALKERSMITH, JA ;
MACDONALD, TT .
GASTROENTEROLOGY, 1994, 106 (06) :1455-1466
[7]
A prospective study of the efficacy and tolerance of a chimeric antibody to tumor necrosis factors (Remicade) in severe pediatric Crohn disease [J].
Cezard, JP ;
Nouaili, N ;
Talbotec, C ;
Hugot, JP ;
Gobert, JG ;
Schmitz, J ;
Mougenot, JF ;
Alberti, C ;
Goulet, O .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2003, 36 (05) :632-636
[8]
The incidence and management of infusion reactions to infliximab: A large center experience [J].
Cheifetz, A ;
Smedley, M ;
Martin, S ;
Reiter, M ;
Leone, G ;
Mayer, L ;
Plevy, S .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (06) :1315-1324
[9]
de Ridder L, 2002, Ned Tijdschr Geneeskd, V146, P1879
[10]
Treatment of inflammatory bowel disease in childhood:: Best available evidence [J].
Escher, JC ;
Taminiau, JAJM ;
Nieuwenhuis, EES ;
Büller, HA ;
Grand, RJ .
INFLAMMATORY BOWEL DISEASES, 2003, 9 (01) :34-58