Development of a sensitive plasma lenvatinib quantification method and validation in thyroid cancer patients.

Authors

Carla Colombo, Roberta Ottria, Matteo Trevisan, Erika Carbone, Claudia Moneta, Marina Lugaresi, Sara Casati, Sofia Vanerio, Daniele Ceruti, Massimiliano Succi, Valentina Cirello, Simone De Leo, Luca Persani, Pierangela Ciuffreda, Laura Fugazzola

Published in

Journal of the Endocrine Society. Volume 10. Issue 8. Pages bvag154. Epub Jul 06, 2026.

Abstract

Lenvatinib (LEN) is effective in the treatment of radioactive iodine refractory differentiated thyroid cancer (DTC), though it is associated with frequent and potentially severe adverse events (AEs). The dose dependency of LEN-related toxicity remains unclear, since no data are available on this topic.
This study aimed to investigate the relationship between LEN dose and plasma concentrations in real-life patients by a novel and validated method for quantifying LEN in plasma samples.
A sensitive high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS) assay for LEN quantification in plasma was set up, with a wide analytical range (0.7-500 ng/mL). Consecutive plasma samples from 19 patients with radioactive iodine-refractory, metastatic DTC were analyzed.
A positive correlation between the administered LEN dose and plasma concentrations was found, particularly in patients on low doses (<18 mg daily). Linear mixed-effects models (LMMs) demonstrated significant interindividual variability in plasma LEN concentrations, contributing to 17% to 28% of the total variance. This variability was more pronounced at higher doses (≥18 mg), being more likely the consequence of LEN-related AEs than of a dose-dependent effect.
This is the first real-life evaluation of interindividual LEN pharmacokinetics variability in advanced DTC patients, obtained by means of the newly developed HPLC-MS/MS method. Our results suggest that the dose-response relationship of LEN in radioactive iodine-refractory DTC may be more complex than previously understood, with substantial interpatient variability and dose-dependent effects. Further studies are needed to determine the implications of our findings in the clinical management of these patients.

PMID:
42459869
Bibliographic data and abstract were imported from PubMed on 16 Jul 2026.

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