Proactive versus Reactive Therapeutic Drug Monitoring: Why, When, and How?

dc.contributor.authorShmais, Manar
dc.contributor.authorRegueiro, Miguel D.
dc.contributor.authorHashash, Jana G.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Gastroenterology and Hepatology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:44:40Z
dc.date.available2025-01-24T11:44:40Z
dc.date.issued2022
dc.description.abstractBackground: Up to a third of inflammatory bowel disease) patients show primary nonresponse to antitumor necrosis factor (anti-TNF) biological therapy, and of those who respond, up to 40% develop secondary loss of response (LOR). Therapeutic drug monitoring (TDM) plays a crucial role in assessing patients with LOR to guide therapy by giving more of the drug or switching to a different biological agent. Although reactive TDM is suggested or recommended by the majority of gastroenterology associations, proactive TDM seems to be more controversial. Summary: In this article, we discuss the updated guidelines on TDM and will also discuss the available data supporting proactive and reactive TDM in patients with Crohn's disease and those with ulcerative colitis using the different available biological agents. Key Messages: Therapeutic drug monitoring (TDM) is a valuable tool to aid in inflammatory bowel disease (IBD) therapy optimization. Reactive TDM is widely accepted in IBD patients with suspected loss of response, especially in those receiving antitumor necrosis factor (anti-TNF) agents. Proactive TDM is emerging as a reasonable approach to patients initiated on anti-TNF therapy, specifically infliximab and, to some extent, adalimumab, particularly for patients with severe ulcerative colitis and fistulizing Crohn's disease. Similarly, TDM may play a role in patients considering de-escalation from combination therapy. To date, proactive TDM is not widely applied to ustekinumab and vedolizumab and more data are required before this becomes part of clinical practice. © 2021 The Author(s) Published by S. Karger AG, Basel.
dc.identifier.doihttps://doi.org/10.1159/000518755
dc.identifier.eid2-s2.0-85123947929
dc.identifier.urihttp://hdl.handle.net/10938/30477
dc.language.isoen
dc.publisherS. Karger AG
dc.relation.ispartofInflammatory Intestinal Diseases
dc.sourceScopus
dc.subjectAnti-drugantibody
dc.subjectBiological
dc.subjectInflammatory bowel disease
dc.subjectTherapeutic drug monitoring
dc.subjectTrough level
dc.subjectAdalimumab
dc.subjectInfliximab
dc.subjectUstekinumab
dc.subjectVedolizumab
dc.subjectBiological therapy
dc.subjectCrohn disease
dc.subjectDrug concentration
dc.subjectDrug monitoring
dc.subjectEnzyme linked immunosorbent assay
dc.subjectGastroenterologist
dc.subjectGel mobility shift assay
dc.subjectHuman
dc.subjectLoss of response
dc.subjectPractice guideline
dc.subjectRadioimmunoassay
dc.subjectReview
dc.subjectTreatment response
dc.subjectTrough concentration
dc.subjectUlcerative colitis
dc.titleProactive versus Reactive Therapeutic Drug Monitoring: Why, When, and How?
dc.typeReview

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