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Review
. 2021 Oct 1;116(10):2014-2025.
doi: 10.14309/ajg.0000000000001396.

A Comprehensive Literature Review and Expert Consensus Statement on Therapeutic Drug Monitoring of Biologics in Inflammatory Bowel Disease

Affiliations
Review

A Comprehensive Literature Review and Expert Consensus Statement on Therapeutic Drug Monitoring of Biologics in Inflammatory Bowel Disease

Adam S Cheifetz et al. Am J Gastroenterol. .

Abstract

Therapeutic drug monitoring (TDM) of biologics is a rapidly evolving field. We aimed to provide a consensus statement regarding the clinical utility of TDM for biologics in inflammatory bowel disease (IBD). A modified Delphi method was applied to develop consensus statements. A comprehensive literature review was performed regarding TDM of biologic therapies in IBD, and 45 statements were subsequently formulated on the potential application of TDM in IBD. The statements, along with literature, were then presented to a panel of 10 gastroenterologists with expertise in IBD and TDM who anonymously rated them on a scale of 1-10 (1 = strongly disagree and 10 = strongly agree). An expert consensus development meeting was held virtually to review, discuss, refine, and reformulate statements that did not meet criteria for agreement or that were ambiguous. During the meeting, additional statements were proposed. Panelists then confidentially revoted, and statements rated ≥7 by 80% or more of the participants were accepted. During the virtual meeting, 8 statements were reworded, 7 new statements were proposed, and 19 statements were rerated. Consensus was finally reached in 48/49 statements. The panel agreed that reactive TDM should be used for all biologics for both primary nonresponse and secondary loss of response. It was recommended that treatment discontinuation should not be considered for infliximab or adalimumab until a drug concentration of at least 10-15 μg/mL was achieved. Consensus was also achieved regarding the utility of proactive TDM for anti-tumor necrosis factor therapy. It was recommended to perform proactive TDM after induction and at least once during maintenance. Consensus was achieved in most cases regarding the utility of TDM of biologics in IBD, specifically for reactive and proactive TDM of anti-tumor necrosis factors.

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Conflict of interest statement

Potential competing interests: K.P. received a lecture fee from Mitsubishi Tanabe Pharma. A.S.C: received consultancy fees from AbbVie, Janssen, Takeda, Bacainn, Arena pharmaceuticals, Grifols, Prometheus, Samsung, Bristol Myers Squibb, and Pfizer, and research support from Inform Diagnostics. A.J.Y. received consultancy fees from Takeda, Prometheus Bioscience and Arena Pharmaceuticals. R.K.C. received consultancy fees from Abbvie, LabCorp, Bristol Myers Squibb, Janssen, Pfizer, Prometheus, Samsung Bioepis, and Takeda. M.T.O. has received consultancy fees for AbbVie, Bristol Myers Squibb, Elan, Genentech/Roche, Janssen, Lycera, Merck, Pfizer, Takeda, and UCB and research grant support from UCB. M.C.D. received consulting fee: Abbvie, Arena, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Eli Lilly, Genentech, Janssen, Pfizer, Prometheus Biosciences, Target RWE, Takeda, UCB. W.A.: received consultancy fees from Abbvie, Amgen, Arena Pharmaceuticals, Dynacare, Janssen, Merck, Novartis, Pfizer, Sandoz, Takeda. C.A.S. has received consultancy fees from Abbvie, BMS, Lilly, Janssen, Pfizer, Prometheus, Takeda, speaker fees for CME activities from Abbvie, Janssen, Pfizer, Takeda, grant support from Abbvie, Pfizer, Takeda and has an equity interest as a co-founder of Mitest Health, LLC. G.Y.M.: received consultancy fees from Boehringer- Ingelheim, Bristol Meyers Squibb/Celgene, Entasis, Genentech, Janssen, Pfizer, Samsung Bioepis, Takeda, Techlab, and research support from Pfizer. MTA has received consultancy fees from Janssen, Prometheus Bioscience, Takeda, Focus Medical Communications, Pfizer, Boehringer Ingelheim Pharmaceuticals, Gilead, Imedex, Cornerstone Health, Inc, Landos Biophama, UCB Biopharma SRL, Eli Lilly, Cosmo Biopharma and grant support from Prometheus Bioscience, Takeda, and Pfizer; E.V.L. received consulting fees from AbbVie, Allergan, Amgen, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Celltrion, Eli Lilly, Genentech, Gilead, Iterative Scopes, Janssen, Pfizer, Takeda, Ono Pharma; research support from AbbVie, Bristol-Myers Squibb, Celgene, Genentech, Gilead, Janssen, Pfizer, Robarts Clinical Trials, Takeda, Theravance and he is a hareholder in Exact Sciences. He is also the Chief Medical Editor of Healio Gastroenterology and Liver Disease. The remaining authors have no conflict of interest.

Comment in

References

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