TDM of cancer therapy: An emerging field

Détails

ID Serval
serval:BIB_BCB55816F337
Type
Actes de conférence (partie): contribution originale à la littérature scientifique, publiée à l'occasion de conférences scientifiques, dans un ouvrage de compte-rendu (proceedings), ou dans l'édition spéciale d'un journal reconnu (conference proceedings).
Sous-type
Abstract (résumé de présentation): article court qui reprend les éléments essentiels présentés à l'occasion d'une conférence scientifique dans un poster ou lors d'une intervention orale.
Collection
Publications
Institution
Titre
TDM of cancer therapy: An emerging field
Titre de la conférence
Journal of Laboratory Medicine
Auteur⸱e⸱s
Widmer N.
Organisation
German Congress of Laboratory Medicine: 15th Annual Congress of the DGKL (German Society of Clinical Chemistry and Laboratory Medicine) and the 3rd Symposium on Biomedical Analysis
Adresse
Mannheim, Germany, September 26-29, 2018
Statut éditorial
Publié
Date de publication
2018
Volume
42
Numéro
4
Pages
eA11
Langue
anglais
Résumé
The therapeutic use of some drugs could be optimized by an individualization of their dosage regimen, based on blood or plasma circulating concentrations measurement in patients thanks to the therapeutic drug monitoring (TDM) feedback strategy. The modern oral targeted anti- cancer drugs are directed against cancer-specific molecules and signaling pathways and seems to be characterized by impressive efficacy and limited non-specific toxicities. Nevertheless, drug resistance, persistence of cancer stem cells, and adverse drug effects still limit their ability to stabilize or cure malignant diseases in the long term.
Oral anticancer drugs are generally licensed for use at fixed doses even though most of them would meet almost all criteria for successful TDM implementation in clinical practice: long-term and continuous therapy, availability of appropriate bioanalytical methods for quantification in clinical samples, high inter-individual pharmacokinetic variability (because of variations in metabolism, protein binding, etc.) but limited intra-individual pharmacokinetic variability, alongside consistent associations between concentration and response. They have also the poten- tial to be involved in multiple interactions (drug–drug; drug–food) and exhibit adherence issues with lifelong treatment. Imatinib was the first to benefit from prospective randomized controlled trial to assess the clinical benefit of a TDM approach, however with contrasting results. Progresses in TDM are still needed, especially for new targeted anticancer agents, both on a conceptual and a practical level. Advances toward modern TDM approaches are ongoing in the field of oncology and other therapeutic area: development of appropriate pharmacokinetic and pharmacokinetic/pharmacodynamic models and improvement of meta-analysis methods to aggregate them, validation of therapeutic target in randomized controlled trials, elaboration of conceptual and practical framework for practitioners and conduct of technological efforts toward miniaturization and development of computer software to assist them.
Open Access
Oui
Création de la notice
22/09/2022 14:42
Dernière modification de la notice
23/09/2022 6:38
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