Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial

被引:3348
作者
Hanauer, SB
Feagan, BG
Lichtenstein, GR
Mayer, LF
Schreiber, S
Colombel, JF
Rachmilewitz, D
Wolf, DC
Olson, A
Bao, WH
Rutgeerts, P
机构
[1] Univ Chicago, Med Ctr, Dept Gastroenterol & Nutr, Chicago, IL 60637 USA
[2] Univ Western Ontario, London Hlth Sci Ctr, London, ON, Canada
[3] Hosp Univ Penn, Dept Gastroenterol, Philadelphia, PA 19104 USA
[4] Mt Sinai Med Ctr, Dept Clin Immunol, New York, NY 10029 USA
[5] Christian Albrechts Univ Kiel Klinikum, Kiel, Germany
[6] CHU Lille, Hop Claude Huriez, F-59037 Lille, France
[7] Tel Aviv Sourasky Med Ctr, Div Med, Tel Aviv, Israel
[8] Atlanta Gastroenterol Associates, Atlanta, GA USA
[9] Centocor Inc, Malvern, PA 19355 USA
[10] Univ Ziekenhuis Gasthuisberg, Afdeling Gastroenterol, Louvain, Belgium
关键词
D O I
10.1016/S0140-6736(02)08512-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background We did a randomised controlled trial to assess the benefit of maintenance infliximab therapy in patients with active Crohn's disease who respond to a single infusion of infliximab. Methods 573 patients with a score of at least 220 on the Crohn's disease activity index (CDAI) received a 5 mg/kg intravenous infusion of infliximab at week 0. After assessment of response at week 2, patients were randomly assigned repeat infusions of placebo at weeks 2 and 6 and then every 8 weeks thereafter until week 46 (group 1), repeat infusions of 5 mg/kg infliximab at the same timepoints (group 11), or 5 mg/kg infliximab at weeks 2 and 6 followed by 10 mg/kg (group 111). The prespecified co-primary endpoints were the proportion of patients who responded at week 2 and were in remission (CDAI <150) at week 30 and the time to loss of response up to week 54 in patients who responded. Analyses of the co-primary endpoints were by intention to treat. Findings 335 (58%) patients responded to a single infusion of infliximab within 2 weeks. At week 30, 23 of 110 (21%) group I patients were in remission, compared with 44 of 113 (39%) group 11 (p=0.003) and 50 of 112 (45%) group III (p=0.0002) patients. Thus, patients in groups 11 and III combined were more likely to sustain clinical remission than patients in group I (odds ratio 2.7, 95% Cl 1.6-4-6). Throughout the 54-week trial, the median time to loss of response was 38 weeks (IQR 15 to >54) and more than 54 weeks (21 to >54) for groups 11 and 111, respectively, compared with 19 weeks (10-45) for group I (p=0.002 and p=0.0002, respectively). Infliximab safety was consistent with that seen in other trials of infliximab in Crohn's disease and rheumatoid arthritis. In particular, the incidence of serious infections was similar across treatment groups. Interpretation Patients with Crohn's disease who respond to an initial dose of infliximab are more likely to be in remission at weeks 30 and 54, to discontinue corticosteroids, and to maintain their response for a longer period of time, if infliximab treatment is maintained every 8 weeks.
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收藏
页码:1541 / 1549
页数:9
相关论文
共 30 条
[1]  
[Anonymous], COCHRANE DATABASE SY, DOI 10.1002/14651858.CD000545
[2]  
Baker DG, 2001, ARTHRITIS RHEUM, V44, pS105
[3]  
Bernstein CN, 2001, CANCER-AM CANCER SOC, V91, P854, DOI 10.1002/1097-0142(20010215)91:4<854::AID-CNCR1073>3.0.CO
[4]  
2-Z
[5]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[6]   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
[7]   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
[8]  
Cohen RD, 2000, AM J GASTROENTEROL, V95, P3469
[9]  
EKBOM A, 1991, CANCER-AM CANCER SOC, V67, P2015, DOI 10.1002/1097-0142(19910401)67:7<2015::AID-CNCR2820670731>3.0.CO
[10]  
2-R