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Updated: Apr 22, 2026

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Tumor necrosis factor-alpha antagonists twenty years later: what do Cochrane reviews tell us?
Anthony A Akobeng1, William J Sandborn, Stephen J Bickston
1*Royal Manchester Children's Hospital, University of Manchester, Manchester, United Kingdom; †Robarts Clinical Trials, Inc., San Diego, California; ‡Division of Gastroenterology, University of California San Diego, La Jolla, California; §Center for Inflammatory Bowel Diseases, Virginia Commonwealth University Health System, Richmond, Virginia; ‖Division of Gastroenterology, Department of Medicine, The University of Western Ontario, London, ON, Canada; ¶Robarts Clinical Trials Inc., Robarts Research Institute, The University of Western Ontario, London, ON, Canada and **Departments of Medicine and Epidemiology and Biostatistics, The University of Western Ontario, London, ON, Canada.
Abstract:
In 1998, the U.S. Food and Drug Administration granted regulatory approval to the first tumor necrosis factor-α antagonist, infliximab, for the treatment of moderately to severely active Crohn's disease. As of 2013, there were 3 additional tumor necrosis factor-α antagonists commercially available for the treatment of inflammatory bowel disease in the United States: adalimumab, certolizumab pegol, and golimumab. Despite a vast literature describing both clinical trial and clinical practice experience with these agents, there remain important questions regarding the efficacy and safety of tumor necrosis factor-α antagonists for the treatment of inflammatory bowel disease. These questions and the best available evidence to answer them were discussed during a Cochrane Collaboration session held at the 2013 Digestive Diseases Week annual meeting. This article reviews the data from that session.
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