Simultaneous determination of folate and methotrexate metabolites in serum by LC-MS/MS during high-dose methotrexate therapy.
Antineoplastic Agents
/ administration & dosage
Chromatography, Liquid
/ methods
Dose-Response Relationship, Drug
Folic Acid
/ administration & dosage
Humans
Methotrexate
/ administration & dosage
Pilot Projects
Precursor Cell Lymphoblastic Leukemia-Lymphoma
/ blood
Tandem Mass Spectrometry
/ methods
Acute lymphoblastic leukemia
Folate cycle metabolites
Folinic acid
High-dose methotrexate
MRM
Tandem mass spectrometry
Journal
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
ISSN: 1873-376X
Titre abrégé: J Chromatogr B Analyt Technol Biomed Life Sci
Pays: Netherlands
ID NLM: 101139554
Informations de publication
Date de publication:
01 Dec 2021
01 Dec 2021
Historique:
received:
20
06
2021
revised:
12
10
2021
accepted:
17
10
2021
pubmed:
16
11
2021
medline:
27
1
2022
entrez:
15
11
2021
Statut:
ppublish
Résumé
High-dose methotrexate (HDMTX) is a central component in the treatment of acute lymphoblastic leukemia, osteosarcoma, and some lymphomas and brain tumors. MTX is given at lethal doses and then is followed by rescue treatment with folinic acid (FA). Despite FA rescue, many patients suffer severe toxicity. The pharmacokinetics of FA rescue have not been sufficiently studied. However, optimization of FA rescue could potentially increase anti-tumor effects, whilst decreasing organ toxicity. Here, we describe our efforts to establish and optimize a liquid chromatography tandem mass spectrometric (LC-MS/MS) method for the simultaneous determination of five essential components of the folate cycle, as well as MTX and its two metabolites. The method was applied to 6 individual patients receiving HDMTX, with 3 or 4 measurements for each patient. The method allows analysis of samples that were initially frozen. This notion, together with the test results in the 6 pilot patients, shows the feasibility of this method to study MTX and FA pharmacokinetics during HDMTX treatment. The method has the potential to optimize HDMTX and FA rescue treatment in individual patients.
Identifiants
pubmed: 34781107
pii: S1570-0232(21)00488-8
doi: 10.1016/j.jchromb.2021.123007
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Folic Acid
935E97BOY8
Methotrexate
YL5FZ2Y5U1
Types de publication
Evaluation Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
123007Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.