The efficacy and safety of a third anti-TNF monoclonal antibody in Crohn's disease after failure of two other anti-TNF antibodies

被引:96
|
作者
Allez, M. [1 ]
Vermeire, S. [2 ]
Mozziconacci, N. [3 ]
Michetti, P. [4 ,5 ]
Laharie, D. [6 ]
Louis, E. [7 ]
Bigard, M. -A. [8 ]
Hebuterne, X. [9 ]
Treton, X. [10 ]
Kohn, A. [11 ]
Marteau, P. [12 ]
Cortot, A. [3 ]
Nichita, C. [4 ,5 ]
van Assche, G. [2 ]
Rutgeerts, P. [2 ]
Lemann, M.
Colombel, J. -F. [3 ]
机构
[1] Univ Paris 07, Hop St Louis, Serv Gastroenterol, APHP, F-75010 Paris, France
[2] Univ Hosp Leuven, Louvain, Belgium
[3] CH & U, Hop Huriez, Lille, France
[4] CHU Vaudois, CH-1011 Lausanne, Switzerland
[5] Univ Lausanne, Lausanne, Switzerland
[6] Hop Haut Leveque, Pessac, France
[7] CHU Sart Tilman, B-4000 Liege, Belgium
[8] Hop Brabois, Vandoeuvre Les Nancy, France
[9] CHU Nice, Hop Archet, Nice, France
[10] Hop Beaujon, Clichy, France
[11] Polo Osped USL RMA, Rome, Italy
[12] Univ Paris 07, Hop Lariboisiere, Paris, France
关键词
ANTITUMOR NECROSIS FACTOR; INFLAMMATORY-BOWEL-DISEASE; CERTOLIZUMAB PEGOL CDP870; FACTOR-ALPHA; MAINTENANCE THERAPY; OPEN-LABEL; CLINICAL-RESPONSE; RANDOMIZED-TRIAL; STURE REGISTRY; LOST RESPONSE;
D O I
10.1111/j.1365-2036.2009.04130.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
P>Background Adalimumab (ADA) and certolizumab pegol (CZP) have demonstrated efficacy in Crohn's disease (CD) patients previously treated with infliximab (IFX). Aim To assess the efficacy and tolerability of a third anti-TNF in CD after failure of and/or intolerance to two different anti-TNF antibodies. Methods Crohn's disease patients who received ADA or CZP after loss of response and/or intolerance to two anti-TNF agent were included in this retrospective study. Data were collected using a standardized questionnaire. Clinical response, duration, safety and reasons for discontinuation were assessed. Results Sixty-seven patients treated with CZP (n = 40) or ADA (n = 27) were included. A clinical response was observed in 41 (61%) at week 6 and 34 patients (51%) at week 20. The probability of remaining under treatment at 3 months, 6 months and 9 months was 68%, 60% and 45%, respectively. At the end of follow-up, the third anti-TNF had been stopped in 36 patients for intolerance (n = 13), or failure (n = 23). Two deaths were observed. Conclusions The treatment with a third anti-TNF (CZP or ADA) agent of CD patients, who have experienced loss of response and/or intolerance to two anti-TNF antibodies, has favourable short-term and long-term efficacy. It is an option to be considered in patients with no other therapeutic options.
引用
收藏
页码:92 / 101
页数:10
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