Tumour necrosis factor inhibitors in inflammatory bowel disease: the story continues

Author:

Peyrin-Biroulet Laurent1,Sandborn William J.2,Panaccione Remo34,Domènech Eugeni567,Pouillon Lieven8,Siegmund Britta9,Danese Silvio1011,Ghosh Subrata1213ORCID

Affiliation:

1. Department of Gastroenterology and Inserm NGERE U1256, University Hospital of Nancy, University of Lorraine, Vandoeuvre-lès-Nancy, France

2. University of California, San Diego, La Jolla, CA, USA

3. Cumming School of Medicine, University of Calgary, Calgary, AB, Canada

4. Inflammatory Bowel Disease Unit, University of Calgary, Calgary, AB, Canada

5. Hospital Universitari Germans Trias i Pujol, Badalona, Spain

6. Departament de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain

7. Centro de Investigación Biomédica en Red sobre enfermedades Hepáticas y Digestivas CIBEREHD, Spain

8. Imelda GI Clinical Research Centre, Imeldaziekenhuis Bonheiden, Bonheiden, Belgium

9. Medizinische Klinik für Gastroenterologie, Infektiologie und Rheumatologie, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany

10. Gastroenterology and Endoscopy, IRCCS Ospedale San Raffaele, Milan, Italy

11. University Vita-Salute San Raffaele, Milan, Italy

12. Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, B15 2TT, UK

13. NIHR Biomedical Research Centre, University of Birmingham and Queen Elizabeth Hospital Birmingham, Birmingham, B15 2TH, UK

Abstract

In the 1990s, tumour necrosis factor-α inhibitor therapy ushered in the biologic therapy era for inflammatory bowel disease, leading to marked improvements in treatment options and patient outcomes. There are currently four tumour necrosis factor-α inhibitors approved as treatments for ulcerative colitis and/or Crohn’s disease: infliximab, adalimumab, golimumab and certolizumab pegol. Despite the clear benefits of tumour necrosis factor-α inhibitors, a subset of patients with inflammatory bowel disease either do not respond, experience a loss of response after initial clinical improvement or report intolerance to anti-tumour necrosis factor-α therapy. Optimizing outcomes of these agents may be achieved through earlier intervention, the use of therapeutic drug monitoring and thoughtful switching within class. To complement these approaches, evolving predictive biomarkers may help inform and optimize clinical decision making by identifying patients who might potentially benefit from an alternative treatment strategy. This review will focus on the current use of tumour necrosis factor-α inhibitors in inflammatory bowel disease and the application of personalized medicine to improve future outcomes for all patients.

Publisher

SAGE Publications

Subject

Gastroenterology

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