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World J Gastroenterol. May 28, 2013; 19(20): 2979-2984
Published online May 28, 2013. doi: 10.3748/wjg.v19.i20.2979
Expert opinion: Experience with 6-mercaptopurine in the treatment of inflammatory bowel disease
Burton I Korelitz
Burton I Korelitz, Clinical Research in Gastroenterology, Division of Gastroenterology, Department of Medicine, Lenox Hill Hospital, New York, NY 10075, United States
Author contributions: Korelitz BI solely contributed to this paper.
Correspondence to: Burton I Korelitz, MD, Chief Emeritus, Director of Clinical Research in Gastroenterology, Division of Gastroenterology, Department of Medicine, Lenox Hill Hospital, New York, NY 10075, United States. bkorelitz@nshs.edu
Telephone: +1-212-4342063 Fax: +1-212-4342446
Received: December 26, 2012
Revised: April 9, 2013
Accepted: April 17, 2013
Published online: May 28, 2013
Abstract

Arbitrarily, modern day treatment of inflammatory bowel disease begins with the introduction of immunosuppressives for ulcerative colitis. Clinical improvement with sulfasalazine had been meaningful but modest. Treatment with adrenocorticotropic hormone and corticosteroids led to clinical responses never before realized but it took much too long to recognize that they were not capable of maintaining remission, that adverse reactions were subtle but potentially devastating and that some other agent would be necessary to capitalize on their transient advantage. This of course was true in the treatment of Crohn’s disease as well. Not much was ever made of the role of sulfasalazine for Crohn’s disease, but with the severing of the diazobond and the elimination of the sulphur component, the 5-aminosalacylic acid (5-ASA) products clearly led to clinical improvement, especially in cases of Crohn’s colitis and those with ileitis where the 5-ASA product was released in the terminal ileum and more proximal in the small bowel as well as in ulcerative colitis. The induction of remission was first demonstrated by 6-mercaptopurine (6-MP) with case reports and uncontrolled trials in patients with ulcerative colitis, but its placebo controlled trial for Crohn’s disease firmly established its role in inducing remission. No subsequent trial has confirmed its similar role for ulcerative colitis, but nevertheless clinicians know well that 6-MP works at least as well and probably more effectively for ulcerative colitis than for Crohn’s disease. What changes have taken place utilizing 6-MP in the management of inflammatory bowel disease since its introduction in the 1960’s and 1970’s and its trial for Crohn’s disease published in the New England Journal of Medicine in 1980?

Keywords: 6-Mercaptopurine, Crohn’s disease, Ulcerative colitis

Core tip: Calculation of dose, utilization of serological tests, maintenance therapy, desensitization to 6-mercaptopurine (6-MP), toxicity to 6-MP, post-operative prevention, extraintestinal manifestations, perirectal fistulas and other fistulas, pregnancy, role of biologicals in management, brand name vs generic 6-MP and azathioprine.