Challenges to the Design, Execution, and Analysis of Randomized Controlled Trials for Inflammatory Bowel Disease

被引:43
作者
D'Haens, Geert [1 ]
Feagan, Brian [2 ,3 ]
Colombel, Jean-Frederic [4 ]
Sandborn, William J. [5 ]
Reinisch, Walter [6 ]
Rutgeerts, Paul [7 ]
Carbonnel, Frank [8 ]
Mary, Jean-Yves [9 ]
Danese, Silvio [10 ]
Fedorak, Richard N. [11 ]
Hanauer, Steven [12 ]
Lemann, Marc [13 ]
机构
[1] Acad Med Ctr, Dept Gastroenterol, NL-1100 DE Amsterdam, Netherlands
[2] Univ Western Ontario, London, ON, Canada
[3] Robarts Clin Trials, London, ON, Canada
[4] CHRU Lille, Lille, France
[5] Univ Calif San Diego, San Diego, CA 92103 USA
[6] Univ Vienna, Vienna, Austria
[7] Catholic Univ Louvain, B-3000 Louvain, Belgium
[8] Hop Univ Paris S, Paris, France
[9] Univ Paris Diderot, INSERM, U717, Paris, France
[10] IRCCS, Ist Clin Humanitas, Milan, Italy
[11] Univ Alberta, Edmonton, AB, Canada
[12] Univ Chicago, Chicago, IL 60637 USA
[13] Hop St Louis, Paris, France
关键词
Inflammatory Bowel Disease; Crohn's Disease; Ulcerative Colitis; Trial Design; Clinical Trials; EFFICACY END-POINTS; CROHNS-DISEASE; ULCERATIVE-COLITIS; CLINICAL-TRIALS; ACTIVITY INDEX; MAINTENANCE THERAPY; CERTOLIZUMAB PEGOL; ENDOSCOPIC INDEX; MEDICAL THERAPY; INFLIXIMAB;
D O I
10.1053/j.gastro.2012.09.031
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Treatment of inflammatory bowel disease has greatly improved with the development of targeted, monoclonal antibody-based therapies. Tumor necrosis factor antagonists are frequently used to treat patients with Crohn's disease or ulcerative colitis, but they have side effects and their efficacy often decreases with use. New, more effective drugs are therefore needed and in development. However, many agents that appeared to be promising in preclinical studies have failed to show efficacy in clinical trials. We discuss possible reasons for the failures of these reagents in trials, which include the high rate of response to placebo, an inadequate range of doses, inappropriate timing of end point measurements, the changing therapeutic environment, and the competitive trial system. We also review regulatory guidelines for end points and trial design and recommend ways to improve trials.
引用
收藏
页码:1461 / 1469
页数:9
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