Therapeutic Drug Monitoring of Biologics During Induction to Prevent Primary Non-Response

Author:

Sparrow Miles P1,Papamichael Konstantinos2,Ward Mark G1,Riviere Pauline3ORCID,Laharie David3,Paul Stephane4,Roblin Xavier5

Affiliation:

1. Department of Gastroenterology, Alfred Hospital and Monash University, Melbourne, Victoria, Australia

2. Division of Gastroenterology, Center for Inflammatory Bowel Disease, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA

3. Gastroenterology Unit, Pessac University Hospital, France

4. Department of Immunology, University Hospital of Saint Etienne, Saint-Etienne, France

5. Gastroenterology Unit, University Hospital of Saint Etienne, Saint-Etienne, France

Abstract

Abstract Biologic therapies have revolutionized the management of inflammatory bowel disease [IBD], but primary and secondary non-responses occur in a significant proportion of patients. Therapeutic drug monitoring [TDM] now has an established role in the treatment algorithm for managing secondary loss of response to anti-tumour necrosis factor [anti-TNF] agents during maintenance therapy. Data to support the use of TDM in the management of secondary loss of response to vedolizumab and ustekinumab are emerging. The potential to prevent primary non-response to biologic agents during induction is of equal, and potentially greater, clinical importance. Again, most data supporting the use of ‘proactive' TDM during induction pertains to the use of anti-TNF agents, but signals of efficacy for the use of TDM during induction with other biologic classes are now appearing. This review aims to summarize data on the use of TDM during induction to prevent pharmacokinetic primary non-response to all three classes of biologic therapy currently available for the treatment of IBD.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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