Multi-model averaging improves the performance of model-guided infliximab dosing in patients with inflammatory bowel diseases.


Journal

CPT: pharmacometrics & systems pharmacology
ISSN: 2163-8306
Titre abrégé: CPT Pharmacometrics Syst Pharmacol
Pays: United States
ID NLM: 101580011

Informations de publication

Date de publication:
08 2022
Historique:
revised: 08 04 2022
received: 08 04 2022
accepted: 05 05 2022
pubmed: 17 6 2022
medline: 19 8 2022
entrez: 16 6 2022
Statut: ppublish

Résumé

Infliximab dosage de-escalation without prior knowledge of drug concentrations may put patients at risk for underexposure and trigger the loss of response. A single-model approach for model-informed precision dosing during infliximab maintenance therapy has proven its clinical benefit in patients with inflammatory bowel diseases. We evaluated the predictive performances of two multi-model approaches, a model selection algorithm and a model averaging algorithm, using 18 published population pharmacokinetic models of infliximab for guiding dosage de-escalation. Data of 54 patients with Crohn's disease and ulcerative colitis who underwent infliximab dosage de-escalation after an earlier escalation were used. A priori prediction (based solely on covariate data) and maximum a posteriori prediction (based on covariate data and trough concentrations) were compared using accuracy and precision metrics and the classification accuracy at the trough concentration target of 5.0 mg/L. A priori prediction was inaccurate and imprecise, with the lowest classification accuracies irrespective of the approach (median 59%, interquartile range 59%-63%). Using the maximum a posteriori prediction, the model averaging algorithm had systematically better predictive performance than the model selection algorithm or the single-model approach with any model, regardless of the number of concentration data. Only a single trough concentration (preferably at the point of care) sufficed for accurate and precise prediction. Predictive performance of both single- and multi-model approaches was robust to the lack of covariate data. Model averaging using four models demonstrated similar predictive performance with a five-fold shorter computation time. This model averaging algorithm was implemented in the TDMx software tool to guide infliximab dosage de-escalation in the forthcoming prospective MODIFI study (NCT04982172).

Identifiants

pubmed: 35706358
doi: 10.1002/psp4.12813
pmc: PMC9381887
doi:

Substances chimiques

Gastrointestinal Agents 0
Infliximab B72HH48FLU

Banques de données

ClinicalTrials.gov
['NCT04982172']

Types de publication

Clinical Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1045-1059

Informations de copyright

© 2022 The Authors. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Wannee Kantasiripitak (W)

Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, Leuven, Belgium.

An Outtier (A)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases and Metabolism, University of Leuven, Leuven, Belgium.

Sebastian G Wicha (SG)

Department of Clinical Pharmacy, Institute of Pharmacy, University of Hamburg, Hamburg, Germany.

Alexander Kensert (A)

Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, Leuven, Belgium.
Department of Chemical Engineering, Vrije Universiteit Brussels, Brussels, Belgium.

Zhigang Wang (Z)

Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, Leuven, Belgium.

João Sabino (J)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases and Metabolism, University of Leuven, Leuven, Belgium.

Séverine Vermeire (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases and Metabolism, University of Leuven, Leuven, Belgium.

Debby Thomas (D)

Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, Leuven, Belgium.

Marc Ferrante (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases and Metabolism, University of Leuven, Leuven, Belgium.

Erwin Dreesen (E)

Department of Pharmaceutical and Pharmacological Sciences, University of Leuven, Leuven, Belgium.

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