Determination of 5-azacitidine in human plasma by LC–MS/MS: application to pharmacokinetics pilot study in MDS/AML patients - Archive ouverte HAL
Article Dans Une Revue Cancer Chemotherapy and Pharmacology Année : 2023

Determination of 5-azacitidine in human plasma by LC–MS/MS: application to pharmacokinetics pilot study in MDS/AML patients

Résumé

Azacitidine (Vidaza®, AZA) is a mainstay for treating acute myeloid leukemia (AML) in patients unfit for standard induction and other myelodysplastic syndromes (MDS). However, only half of the patients usually respond to this drug and almost all patients will eventually relapse. Predictive markers for response to AZA are yet to be identified. AZA is metabolized in the liver by a single enzyme, cytidine deaminase (CDA). CDA is a ubiquitous enzyme coded by a highly polymorphic gene, with subsequent great variability in resulting activities in the liver. The quantitative determination of AZA in plasma is challenging due the required sensitivity and because of the instability in the biological matrix upon sampling, possibly resulting in erratic values.
Fichier non déposé

Dates et versions

hal-04352302 , version 1 (19-12-2023)

Identifiants

Citer

Melanie Donnette, Loic Osanno, Madeleine Giocanti, Geoffroy Venton, Laure Farnault, et al.. Determination of 5-azacitidine in human plasma by LC–MS/MS: application to pharmacokinetics pilot study in MDS/AML patients. Cancer Chemotherapy and Pharmacology, 2023, 91 (3), pp.231-238. ⟨10.1007/s00280-023-04505-y⟩. ⟨hal-04352302⟩
49 Consultations
0 Téléchargements

Altmetric

Partager

More