Systematic review: does concurrent therapy with 5-ASA and immunomodulators in inflammatory bowel disease improve outcomes?

被引:49
作者
Andrews, J. M. [1 ]
Travis, S. P. L. [2 ]
Gibson, P. R. [3 ]
Gasche, C. [4 ,5 ]
机构
[1] Univ Adelaide, Adelaide, SA, Australia
[2] John Radcliffe Hosp, Gastroenterol Unit, Oxford OX3 9DU, England
[3] Monash Univ, Dept Med, Box Hill Hosp, Melbourne, Vic 3004, Australia
[4] Med Univ Vienna, Dept Med 3, Div Gastroenterol & Hepatol, Vienna, Austria
[5] Med Univ Vienna, Christian Doppler Lab Mol Canc Chemoprevent, Vienna, Austria
基金
奥地利科学基金会;
关键词
COLORECTAL-CANCER RISK; COLITIS PRACTICE GUIDELINES; EVIDENCE-BASED CONSENSUS; ULCERATIVE-COLITIS; CROHNS-DISEASE; 5-AMINOSALICYLIC ACID; MAINTENANCE TREATMENT; CONTROLLED-TRIAL; MMX MESALAMINE; OLMSTED COUNTY;
D O I
10.1111/j.1365-2036.2008.03915.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
With greater use of immunomodulators in inflammatory bowel disease (IBD), it is uncertain whether concurrent therapy with both 5-aminosalicylic acid [5-ASA, mesalazine (mesalamine)] and an immunomodulator is necessary. To determine whether concurrent therapy with both 5-ASA and immunomodulator(s) improves outcomes in IBD. Systematic review with search terms 'azathioprine, 6-mercaptopurine, thiopurine(s), 5 aminosalicylic acid, mesalazine, inflammatory bowel disease, ulcerative colitis, Crohn's disease, immunosuppressant(s), immunomodulator and methotrexate' in November 2007 to identify clinical trials on concurrent 5-ASA and immunomodulator therapy. Two small controlled studies were found. Neither showed a benefit on disease control beyond immunomodulator monotherapy. Potential pharmacological interactions exist between 5-ASA and thiopurines. Whilst circumstantial, epidemiological and laboratory evidence suggests that 5-ASA may assist colorectal cancer (CRC) chemoprevention, it may simply be via anti-inflammatory effects. With changes in practice, ethical issues and the long lead-time needed to demonstrate or disprove an effect, no clinical studies can/will directly answer this. The costs of avoiding one CRC in IBD may be as low as 153 times the annual cost of 5-ASA therapy. It is unclear whether concurrent 5-ASA and immunomodulator therapy improves outcomes of disease control, drug toxicity or compliance. Concurrent therapy of 5-ASA and immunomodulators may decrease CRC risk at 'acceptable' cost.
引用
收藏
页码:459 / 469
页数:11
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