Therapeutic drug monitoring in oncology: International Association of Therapeutic Drug Monitoring and Clinical Toxicology consensus guidelines for imatinib therapy.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
11 2021
Historique:
received: 25 06 2021
revised: 17 08 2021
accepted: 19 08 2021
pubmed: 2 10 2021
medline: 15 12 2021
entrez: 1 10 2021
Statut: ppublish

Résumé

Although therapeutic drug monitoring (TDM) is an important tool in guiding drug dosing for other areas of medicine including infectious diseases, cardiology, psychiatry and transplant medicine, it has not gained wide acceptance in oncology. For imatinib and other tyrosine kinase inhibitors, a flat dosing approach is utilised for management of oral chemotherapy. There are many published studies examining the correlation of blood concentrations with clinical effects of imatinib. The International Association of Therapeutic Drug Monitoring and Clinical Toxicology (IATDMCT) determined that there was a need to examine the published literature regarding utility of TDM in imatinib therapy and to develop consensus guidelines for TDM based on the available data. This article summarises the scientific evidence regarding TDM of imatinib, as well as the consensus guidelines developed by the IATDMCT.

Identifiants

pubmed: 34597977
pii: S0959-8049(21)00560-8
doi: 10.1016/j.ejca.2021.08.033
pii:
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Imatinib Mesylate 8A1O1M485B

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

428-440

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Conflict of interest statement W.A.C., E.C., A.K.F. and J.H.M. have no declared conflicts of interest in relation to this work. RJHM has no conflicts of interest in relation to this work. However, his institution has received research funding for investigator-initiated research from Astellas, Bayer, Boehringer Ingelheim, Cristal Therapeutics, Novartis, PamGene, Pfizer, Roche, Sanofi and Servier. R.A.L. has acted as a consultant or advisor to Amgen, Ariad/Takeda, Astellas, Celgene/Bristol Myers Squibb, CVS/Caremark, Epizyme, MorphoSys and Novartis and has received clinical research support to his institution from Astellas, Celgene, Cellectis, Daiichi Sankyo, Forty Seven/Gilead, Novartis and Rafael Pharmaceuticals and royalties from UpToDate. S.J.S. is the founder and CEO of Saladax Biomedical, Inc.

Auteurs

William A Clarke (WA)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: wclarke@jhmi.edu.

Etienne Chatelut (E)

Université de Toulouse, Inserm, Institut Claudius-Regaud, Toulouse, France.

Alan K Fotoohi (AK)

Division of Clinical Pharmacology, Department of Laboratory Medicine, Karolinska Institute, Karolinska University Hospital, Huddinge, Stockholm, 141 86, Sweden.

Richard A Larson (RA)

Department of Medicine and Comprehensive Cancer Center, University of Chicago, Chicago, IL, USA.

Jennifer H Martin (JH)

Centre for Drug Repurposing and Medicines Research, University of Newcastle. Level 3, Hunter Medical Research Institute, New Lambton Heights, 2305, New South Wales, Australia. Electronic address: https://twitter.com/jenhelenmar.

Ron H J Mathijssen (RHJ)

Department of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, the Netherlands.

Salvatore J Salamone (SJ)

Saladax Biomedical Inc., Bethlehem, PA, USA.

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Classifications MeSH