Real-World Infliximab Pharmacokinetic Study Informs an Electronic Health Record-Embedded Dashboard to Guide Precision Dosing in Children with Crohn's Disease.
Antibodies
/ analysis
Area Under Curve
Biomarkers
/ blood
Blood Sedimentation
Child
Crohn Disease
/ drug therapy
Electronic Health Records
Gastrointestinal Agents
/ administration & dosage
Humans
Infliximab
/ administration & dosage
Neutrophils
/ chemistry
Receptors, IgG
/ blood
Serum Albumin
/ analysis
Journal
Clinical pharmacology and therapeutics
ISSN: 1532-6535
Titre abrégé: Clin Pharmacol Ther
Pays: United States
ID NLM: 0372741
Informations de publication
Date de publication:
06 2021
06 2021
Historique:
received:
10
11
2020
accepted:
27
11
2020
pubmed:
24
12
2020
medline:
11
9
2021
entrez:
23
12
2020
Statut:
ppublish
Résumé
Standard-of-care infliximab dosing regimens were developed prior to the routine use of therapeutic drug monitoring and identification of target concentrations. Not surprisingly, subtherapeutic infliximab concentrations in pediatric Crohn's disease (CD) are common. The primary aim was to conduct a real-world pharmacokinetic (PK) evaluation to discover blood biomarkers of rapid clearance, identify exposure targets, and a secondary aim to translate PK modeling to the clinic. In a multicenter observational study, 671 peak and trough infliximab concentrations from 78 patients with CD were analyzed with a drug-tolerant assay (Esoterix; LabCorp, Calabasas, CA). Individual area under the curve (AUC) estimates were generated as a measure of drug exposure over time. Population PK modeling (nonlinear mixed-effect modeling) identified serum albumin, antibody to infliximab, erythrocyte sedimentation rate (ESR), and neutrophil CD64 as biomarkers for drug clearance. Week 14 and week 52 biochemical remitters (fecal calprotectin < 250 µg/g) had higher infliximab exposure (AUC) throughout induction. The optimal infliximab AUC target during induction for week 14 biochemical remission was 79,348 µg*h/mL (area under the receiver operating characteristic curve (AUROC) 0.77, [0.63-0.90], 85.7% sensitive, and 64.3% specific) with those exceeding the AUC target more likely to achieve a surgery-free week 52 biochemical remission (OR 4.3, [1.2-14.6]). Pretreatment predictors for subtherapeutic week 14 AUC included neutrophil CD64 > 6 (OR 4.5, [1.4-17.8]), ESR > 30 mm/h (OR 3.8, [1.4-11]), age < 10 years old (OR 4.2, [1.2-20]), and weight < 30 kg (OR 6.6, [2.1-25]). We created a decision-support PK dashboard with an iterative process and embedded the modeling program within the electronic health record. Model-informed precision dosing guided by real-world PKs is now available at the bedside in real-time.
Identifiants
pubmed: 33354765
doi: 10.1002/cpt.2148
pmc: PMC8159860
mid: NIHMS1680055
doi:
Substances chimiques
Antibodies
0
Biomarkers
0
Gastrointestinal Agents
0
Receptors, IgG
0
Serum Albumin
0
Infliximab
B72HH48FLU
Types de publication
Journal Article
Multicenter Study
Observational Study
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1639-1647Subventions
Organisme : NICHD NIH HHS
ID : T32 HD069054
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007727
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK078392
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK105229
Pays : United States
Organisme : NIDDK NIH HHS
ID : R03 DK118314
Pays : United States
Informations de copyright
© 2020 The Authors. Clinical Pharmacology & Therapeutics © 2020 American Society for Clinical Pharmacology and Therapeutics.
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