Population Pharmacokinetics of Ibrutinib in Healthy Adults
Autor: | Isam I. Salem, Mohammad Saleh, Mutasim Al-Ghazawi, Omaima Najib, Naji M. Najib |
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Rok vydání: | 2021 |
Předmět: |
Pharmacology
Oncology education.field_of_study medicine.medical_specialty Clinical chemistry business.industry Population Population pharmacokinetics 030226 pharmacology & pharmacy Clinical trial 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Pharmacokinetics chemistry Oral administration 030220 oncology & carcinogenesis Internal medicine Ibrutinib medicine Pharmacology (medical) Dosing education business |
Zdroj: | European Journal of Drug Metabolism and Pharmacokinetics. 46:405-413 |
ISSN: | 2107-0180 0378-7966 |
DOI: | 10.1007/s13318-021-00679-z |
Popis: | Ibrutinib is an antineoplastic agent that reduces B-cell proliferation by inhibiting Bruton's tyrosine kinase. We describes population pharmacokinetics of ibrutinib in healthy adults, and explores potential patient characteristics associated with ibrutinib pharmacokinetics. A population pharmacokinetic modeling approach was applied to 39 healthy subjects. Modeling was performed using Monolix (v.2019R2). Serial blood samples to measure the plasma ibrutinib concentration were collected following the oral administration of 140 mg ibrutinib on two different occasions under fasting conditions. Demographic and clinical information were evaluated as possible predictors of ibrutinib pharmacokinetics during model development. Simulations (using mlxR: R package v.4.0.2) following the administration of therapeutic doses were performed to explore the clinical implications of identified covariates on ibrutinib steady-state concentrations. A two-compartment model with zero order absorption best fit the data. Inter-individual and inter-occasion variability were quantified by the proposed model. We identified smoking status as a significant covariate associated with ibrutinib clearance. Smoking was found to increase ibrutinib clearance by approximately 60%, which resulted in a reduction in simulated steady-state concentrations by around 40%. The model can be used to simulate clinical trials or various dosing scenarios. The proposed model can be used to optimize ibrutinib dosing based on the smoking status. |
Databáze: | OpenAIRE |
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