Evidence map›Paper›PMID 38006575›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2024

Pharmacokinetics of Imatinib Mesylate and Development of Limited Sampling Strategies for Estimating the Area under the Concentration-Time Curve of Imatinib Mesylate in Palestinian Patients with Chronic Myeloid Leukemia.

Deema Hilmi Adawi, Nadia Ben Fredj, Ahmad Al-Barghouthi, Ichrack Dridi, Mustafa Lubada, Mohammad Manasra, Karim Aouam

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Article in European journal of drug metabolism and pharmacokinetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Deema Hilmi AdawiDepartment of Pharmacology, Faculty of Pharmacy, University of Monastir, Monastir, Tunisia. Deema.hilmi.adawi@gmail.com.ORCID http://orcid.org/0009-0008-2281-2655
Nadia Ben FredjDepartment of Pharmacology, Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
Ahmad Al-BarghouthiDepartment of Pharmacology, Palestinian Ministry of Health, Ramallah, Palestine.
Ichrack DridiDepartment of Pharmacology, Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.
Mustafa LubadaDepartment of Pharmacology, Palestinian Ministry of Health, Ramallah, Palestine.
Mohammad ManasraDepartment of Pharmacology, Palestinian Ministry of Health, Ramallah, Palestine.
Karim AouamDepartment of Pharmacology, Faculty of Pharmacy, University of Monastir, Monastir, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveImatinib is a tyrosine kinase inhibitor used in the treatment of chronic myeloid leukemia (CML). The area under the concentration-time curve (AUC) is a pharmacokinetic parameter that symbolizes overall exposure to a drug, which is correlated with complete cytogenetic and treatment responses to imatinib, as well as its side effects in patients with CML. The limited sampling strategy (LSS) is considered a sufficiently precise and practical method that can be used to estimate pharmacokinetic parameters such as AUC, without the need for frequent, costly, and inconvenient blood sampling. This study aims to investigate the pharmacokinetic parameters of imatinib, develop and validate a reliable and practical LSS for estimating imatinib AUC

methodPharmacokinetic profiles, involving six blood samples collected during a 24-h dosing interval, were obtained from 25 Palestinian patients diagnosed with CML who had been receiving imatinib for at least 7 days and had reached a steady-state level. Imatinib AUC

resultsAmong the one-timepoint estimations, predicted AUC

conclusionThe LSS using one timepoint, especially C

Indexed as

ArabsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveArea Under CurveDrug MonitoringHumansImatinib MesylateImmunosuppressive AgentsReproducibility of ResultsImatinib MesylateImmunosuppressive Agents

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.