Evidence map›Paper›PMID 39749370›Full record

ArticleFundamental & clinical pharmacology2025

Body mass index affects imatinib exposure: Real-world evidence from TDM with adaptive dosing.

Paul Maroselli, Raphaelle Fanciullino, Julien Colle, Laure Farnault, Pauline Roche, Geoffroy Venton, Régis Costello, Joseph Ciccolini

Abstract read
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Article in Fundamental & clinical pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Paul MaroselliPRISM Biogénopôle La Timone University Hospital of Marseille, APHM, Marseille, France.
Raphaelle FanciullinoCOMPO Centre de Recherche en Cancérologie de Marseille Inserm U1068, Marseille, France.
Julien ColleHematology Dept, La Conception University Hospital of Marseille APHM, Marseille, France.
Laure FarnaultHematology Dept, La Conception University Hospital of Marseille APHM, Marseille, France.
Pauline RochePharmacy Unit, La Conception University Hospital of Marseille APHM, Marseille, France.
Geoffroy VentonHematology Dept, La Conception University Hospital of Marseille APHM, Marseille, France.
Régis CostelloHematology Dept, La Conception University Hospital of Marseille APHM, Marseille, France.
Joseph CiccoliniPRISM Biogénopôle La Timone University Hospital of Marseille, APHM, Marseille, France.ORCID https://orcid.org/0000-0003-1733-3410

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImatinib is the treatment of elderly or frail patients with chronic myeloid leukemia (CML). Trough levels of around 1000 ng/ml are considered as the target exposure.

objectivesWe searched for baseline parameters associated with imatinib pharmacokinetics, and studied the clinical impact of subsequent adaptive dosing.

methodsWe present data from 60 adult CML patients upon imatinib with therapeutic drug monitoring (TDM) and adaptive dosing.

resultsMean trough levels after treatment initiation were 994.2 ± 560.6 ng/ml with 56% inter-patient variability). Only 29% of patients were in the therapeutic range. Body weight, height, body surface area, body mass index (BMI), and age were associated with imatinib plasma levels on univariate analysis. Age and BMI remained the only parameters associated with imatinib trough levels on multivariate analysis. As severe toxicities have been previously reported in patients with low BMI treated with standard imatinib, we evaluated the extent to which low BMI may lead to plasma overexposure. We found a statistically significant difference in trough imatinib levels in patients with BMI < 18.5 kg/m

conclusionOur data suggest that low BMI has a significant impact on imatinib exposure but that pharmacokinetically-guided dosing limits its clinical impact in patients.

Indexed as

Antineoplastic AgentsBody Mass IndexDrug MonitoringImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAdultAgedAged, 80 and overAge FactorsDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedRetrospective StudiesAntineoplastic AgentsImatinib Mesylateadaptive dosingbody mass indexImatinibpharmacokineticstherapeutic drug monitoring

Identifiers

PMID39749370
PMCPMC11696203

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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.