Use of methotrexate in refractory Crohn's disease: The Edinburgh experience

被引:26
作者
Din, Shahida [1 ]
Dahele, Anna [1 ]
Fennel, Janice [1 ]
Aitken, Sue [1 ]
Shand, Alan G. [1 ]
Arnott, Ian D. R. [1 ]
Satsangi, Jack [1 ]
机构
[1] Univ Edinburgh, Mol Med Ctr, Gastrointestinal Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
Crohn's disease; refractory; methotrexate;
D O I
10.1002/ibd.20405
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: In the two benchmark controlled trials in Crohn's disease (CD) supporting its use, methotrexate (MTX) was used as the immunosuppressant of choice in immunomodulatory-naive patients. However, in daily clinical practice MTX is used generally after thiopurine analogs have failed. Methods: The data are reported using intramuscular (IM) MTX (25 mg/week) in the induction of remission and oral MTX (15 mg/week) in 39 CD patients with a median age of 32 years, assessed retrospectively. In all, 97% patients had failed azathioprine and/or mercaptopurine therapy due to lack of efficacy in 14 (36%) and side effects in 24 (61%) patients; 21 patients (53%) were steroid-dependent with a median dose of 27.5 mg prednisolone/clay for over a year. Results: In all, 72% of patients tolerated an induction regimen of 25 mg/week of IM MTX; 10% managed a reduced dose and 18% were intolerant. Remission was achieved in 71% of patients at 16 weeks. In the patients taking corticosteroids, withdrawal was achieved in 26% of patients and reduction in 47% at 16 weeks. Oral MTX therapy was continued in 22 patients after induction. In this group the probability of relapse was 78% at 50 weeks of oral therapy. Conclusions: Parenteral MTX therapy is efficacious in inducing remission in steroid-dependent CD patients, although its use is limited by side effects in approximate to 30% of patients. Low-dose oral therapy does not maintain long-term remission and is not a suitable alternative.
引用
收藏
页码:756 / 762
页数:7
相关论文
共 29 条
[1]
Alfaro J, 2000, REV MED CHILE, V128, P315
[2]
Arora S, 1999, HEPATO-GASTROENTEROL, V46, P1724
[3]
Methotrexate-induced optic neuropathy [J].
Balachandran, C ;
McCluskey, PJ ;
Champion, GD ;
Halmagyi, GM .
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2002, 30 (06) :440-441
[4]
LOW-DOSE ORAL METHOTREXATE IN REFRACTORY INFLAMMATORY BOWEL-DISEASE [J].
BARON, TH ;
TRUSS, CD ;
ELSON, CO .
DIGESTIVE DISEASES AND SCIENCES, 1993, 38 (10) :1851-1856
[5]
PHARMACOKINETICS OF METHOTREXATE ADMINISTERED BY INTRAMUSCULAR AND SUBCUTANEOUS INJECTIONS IN PATIENTS WITH RHEUMATOID-ARTHRITIS [J].
BROOKS, PJ ;
SPRUILL, WJ ;
PARISH, RC ;
BIRCHMORE, DA .
ARTHRITIS AND RHEUMATISM, 1990, 33 (01) :91-94
[6]
CHAMIOTPRIEUR C, 1993, GASTROENTEROLOGY, V104, pA680
[7]
A survey of Canadian gastroenterologists about the use of methotrexate in patients with Crohn's disease [J].
Chande, N ;
Ponich, T ;
Gregor, J .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2005, 19 (09) :553-558
[8]
Efficacy of parenteral methotrexate in refractory Crohn's disease [J].
Chong, RY ;
Hanauer, SB ;
Cohen, RD .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (01) :35-44
[9]
Methotrexate for inflammatory bowel disease: Pharmacology and preliminary results [J].
Egan, LJ ;
Sandborn, WJ .
MAYO CLINIC PROCEEDINGS, 1996, 71 (01) :69-80
[10]
Intravenous hydrocortisone premedication reduces antibodies to infliximab in Crohn's disease: A randomized controlled trial [J].
Farrell, RJ ;
Alsahli, M ;
Jeen, YT ;
Falchuk, KR ;
Peppercorn, MA ;
Michetti, P .
GASTROENTEROLOGY, 2003, 124 (04) :917-924