The London Position Statement of the World Congress of Gastroenterology on Biological Therapy for IBD With the European Crohn's and Colitis Organization: When to Start, When to Stop, Which Drug to Choose, and How to Predict Response

被引:329
作者
D'Haens, Geert R. [1 ]
Panaccione, Remo [2 ]
Higgins, Peter D. R. [3 ]
Vermeire, Severine [4 ]
Gassull, Miquel [5 ]
Chowers, Yehuda [6 ]
Hanauer, Stephen B. [7 ]
Herfarth, Hans [8 ]
Hommes, Daan W. [9 ]
Kamm, Michael [10 ,11 ]
Lofberg, Robert [12 ]
Quary, A. [13 ]
Sands, Bruce [14 ]
Sood, A. [15 ]
Watermayer, G. [16 ,17 ]
Lashner, Bret [18 ]
Lemann, Marc [19 ]
Plevy, Scott [20 ]
Reinisch, Walter [21 ]
Schreiber, Stefan [22 ]
Siegel, Corey [23 ]
Targan, Stephen [24 ]
Watanabe, M. [25 ]
Feagan, Brian [26 ]
Sandborn, William J. [27 ]
Colombel, Jean Frederic [28 ]
Travis, Simon [29 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Gastroenterol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Calgary, Inflammatory Bowel Dis Clin, Calgary, AB, Canada
[3] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[4] Univ Hosp Gasthuisberg, Dept Gastroenterol, B-3000 Louvain, Belgium
[5] Germans Trias & Pujol Fdn, Hlth Sci Res Inst, Badalona, Spain
[6] Rambam Hlth Care Campus, Dept Gastroenterol, Haifa, Israel
[7] Univ Chicago, Med Ctr, Sect Gastroenter Hepatol & Nutr, Chicago, IL 60637 USA
[8] Univ N Carolina, Div Gastroenterol & Hepatol, Chapel Hill, NC USA
[9] Leiden Univ, Med Ctr, Dept Gastroenterol, Leiden, Netherlands
[10] St Vincents Hosp, Dept Med, Melbourne, Vic, Australia
[11] Univ London Imperial Coll Sci Technol & Med, London, England
[12] IBD Unit, Stockholm, Sweden
[13] King Abdulaziz Univ Hosp, Jeddah, Saudi Arabia
[14] Massachusetts Gen Hosp, MGH Crohns & Colitis Ctr, Boston, MA 02114 USA
[15] Dayanand Med Coll & Hosp, Dept Gastroenterol, Ludhiana, Punjab, India
[16] Groote Schuur Hosp, Div Gastroenterol, ZA-7925 Cape Town, South Africa
[17] Groote Schuur Hosp, Dept Med, ZA-7925 Cape Town, South Africa
[18] Cleveland Clin, Dept Gastroenterol, Cleveland, OH 44106 USA
[19] Hosp St Louis, Dept Gastroenterol, Paris, France
[20] UNC Sch Med, Chapel Hill, NC USA
[21] Med Univ Vienna, Div Gastroenterol & Hepatol, Dept Internal Med 3, Vienna, Austria
[22] Univ Hosp Schleswig Holstein UKSH, Dept Gen Internal Med, Kiel, Germany
[23] Dartmouth Hitchcock Med Ctr, Sect Gastroenterol & Hepatol, Lebanon, NH 03766 USA
[24] Cedars Sinai Med Ctr, Ctr Inflammatory Bowel Dis, Los Angeles, CA 90048 USA
[25] Tokyo Med & Dent Univ, Dept Gastroenterol & Hepatol, Tokyo, Japan
[26] Univ Western Ontario, London, ON, Canada
[27] Mayo Clin, Rochester, MN USA
[28] Hosp Huriez, Dept Hepatogastroenterol, Lille, France
[29] John Radcliffe Hosp, Gastroenterol Unit, Oxford OX3 9DU, England
关键词
INFLAMMATORY-BOWEL-DISEASE; TUMOR-NECROSIS-FACTOR; SCHEDULED MAINTENANCE TREATMENT; MONOCLONAL-ANTIBODY ADALIMUMAB; EVIDENCE-BASED CONSENSUS; POPULATION-BASED COHORT; QUALITY-OF-LIFE; TERM-FOLLOW-UP; LONG-TERM; CERTOLIZUMAB PEGOL;
D O I
10.1038/ajg.2010.392
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
The advent of biological therapy has revolutionized inflammatory bowel disease (IBD) care. Nonetheless, not all patients require biological therapy. Selection of patients depends on clinical characteristics, previous response to other medical therapy, and comorbid conditions. Availability, reimbursement guidelines, and patient preferences guide the choice of first-line biological therapy for luminal Crohn's disease (CD). Infliximab (IFX) has the most extensive clinical trial data, but other biological agents (adalimumab (ADA), certolizumab pegol (CZP), and natalizumab (NAT)) appear to have similar benefits in CD. Steroid-refractory, steroid-dependent, or complex fistulizing CD are indications for starting biological therapy, after surgical drainage of any sepsis. For fistulizing CD, the efficacy of IFX for inducing fistula closure is best documented. Unique risks of NAT account for its labeling as a second-line biological agent in some countries. Patients who respond to induction therapy benefit from systematic re-treatment. The combination of IFX with azathioprine is better than monotherapy for induction of remission and mucosal healing up to 1 year in patients who are naive to both agents. Whether this applies to other agents remains unknown. IFX is also effective for treatment-refractory, moderate, or severely active ulcerative colitis. Patients who have a diminished or loss of response to anti-tumor necrosis factor (TNF) therapy may respond to dose adjustment of the same agent or switching to another agent. Careful consideration should be given to the reasons for loss of response. There are insufficient data to make recommendations on when to stop anti-TNF therapy. Preliminary evidence suggests that a substantial proportion of patients in clinical remission for > 1 year, without signs of active inflammation can remain in remission after stopping treatment.
引用
收藏
页码:199 / 212
页数:14
相关论文
共 132 条
[1]
Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease [J].
Abreu, MT ;
Taylor, KD ;
Lin, YC ;
Hang, T ;
Gaiennie, J ;
Landers, CJ ;
Vasiliauskas, EA ;
Kam, LY ;
Rojany, M ;
Papadakis, KA ;
Rotter, JI ;
Targan, SR ;
Yang, HY .
GASTROENTEROLOGY, 2002, 123 (03) :679-688
[2]
Clinical Utility of Measuring Infliximab and Human Anti-Chimeric Antibody Concentrations in Patients With Inflammatory Bowel Disease [J].
Afif, Waqqas ;
Loftus, Edward V., Jr. ;
Faubion, William A. ;
Kane, Sunanda V. ;
Bruining, David H. ;
Hanson, Karen A. ;
Sandborn, William J. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2010, 105 (05) :1133-1139
[3]
The efficacy and safety of a third anti-TNF monoclonal antibody in Crohn's disease after failure of two other anti-TNF antibodies [J].
Allez, M. ;
Vermeire, S. ;
Mozziconacci, N. ;
Michetti, P. ;
Laharie, D. ;
Louis, E. ;
Bigard, M. -A. ;
Hebuterne, X. ;
Treton, X. ;
Kohn, A. ;
Marteau, P. ;
Cortot, A. ;
Nichita, C. ;
van Assche, G. ;
Rutgeerts, P. ;
Lemann, M. ;
Colombel, J. -F. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2009, 31 (01) :92-101
[4]
Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence [J].
Alvarez-Lobos, M ;
Arostegui, JI ;
Sans, M ;
Tassies, D ;
Plaza, S ;
Delgado, S ;
Lacy, AM ;
Pique, JM ;
Yagüe, J ;
Panés, J .
ANNALS OF SURGERY, 2005, 242 (05) :693-700
[5]
[Anonymous], COCHRANE DATABASE SY
[6]
Mucosal gene signatures to predict response to infliximab in patients with ulcerative colitis [J].
Arijs, I. ;
Li, K. ;
Toedter, G. ;
Quintens, R. ;
Van Lommel, L. ;
Van Steen, K. ;
Leemans, P. ;
De Hertogh, G. ;
Lemaire, K. ;
Ferrante, M. ;
Schnitzler, F. ;
Thorrez, L. ;
Ma, K. ;
Song, X. -Y R. ;
Marano, C. ;
Van Assche, G. ;
Vermeire, S. ;
Geboes, K. ;
Schuit, F. ;
Baribaud, F. ;
Rutgeerts, P. .
GUT, 2009, 58 (12) :1612-1619
[7]
An analysis of factors influencing short-term and sustained response to infliximab treatment for Crohn's disease [J].
Arnott, IDR ;
McNeill, G ;
Satsangi, J .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (12) :1451-1457
[8]
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
[9]
Predictors of Crohn's disease [J].
Beaugerie, L ;
Seksik, P ;
Nion-Larmurier, I ;
Gendre, JP ;
Cosnes, J .
GASTROENTEROLOGY, 2006, 130 (03) :650-656
[10]
Bokemeyer BKA, 2009, Journal of Crohn's and Colitis, V3, pS82