Tyrosine Kinase Inhibitors in Cancers: Treatment optimization - Part II.

efficacy pharmacokinetics therapy management variability

Journal

Critical reviews in oncology/hematology
ISSN: 1879-0461
Titre abrégé: Crit Rev Oncol Hematol
Pays: Netherlands
ID NLM: 8916049

Informations de publication

Date de publication:
27 May 2024
Historique:
received: 24 01 2024
revised: 02 05 2024
accepted: 03 05 2024
medline: 30 5 2024
pubmed: 30 5 2024
entrez: 29 5 2024
Statut: aheadofprint

Résumé

Real-life populations are more heterogeneous than those included in prospective clinical studies. In cancer patients, comorbidities and co-medications favor the appearance of severe adverse effects which can significantly impact quality of life and treatment effectiveness. Most of tyrosine kinase inhibitors (TKI) have been developed with flat oral dosing exposing patients to the risk of poor adherence due to side effects. Additionally, genetic or physiological factors, differences in diet, and drug-drug interactions can lead to inter-individual variability affecting treatment outcomes and increasing the risk of adverse events. Knowledge of the different factors of variability allows individualized patient management. This review examines the effects of adherence, food intake, and pharmaceutical form on the pharmacokinetics of oral TKI, as well as evaluating pharmacokinetics considerations improving TKI management. Concentration-effectiveness and concentration-toxicity data are presented for the selected TKI, and a simple therapeutic drug monitoring schema is outlined to help individualize dosing of oral TKI.

Identifiants

pubmed: 38810843
pii: S1040-8428(24)00128-8
doi: 10.1016/j.critrevonc.2024.104385
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

104385

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: CL has benefitted from assistance from BMS, MSD, Novartis, Amgen, Roche, Avantis Medical Systems, Pierre Fabre, Pfizer and Incyte. NM declare has benefited from assistance from BMS, MSD, Novartis, Pierre Fabre, Sanofi, Merck and Sun Pharma. Conflict of interest CL has benefitted from assistance from BMS, MSD, Novartis, Amgen, Roche, Avantis Medical Systems, Pierre Fabre, Pfizer and Incyte. NM declare has benefited from assistance from BMS, MSD, Novartis, Pierre Fabre, Sanofi, Merck and Sun Pharma. FF declare the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Florent Ferrer (F)

Department of Pharmacology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France; SMARTc Unit, CRCM Inserm U1068, Aix Marseille Univ and APHM, Marseille, France; Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France.

Pauline Tetu (P)

Department of Dermatology, APHP Dermatology, Paris 7 Diderot University, INSERM U976, Hôpital Saint-Louis, Paris, France; Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France.

Léa Dousset (L)

Dermatology Department, Bordeaux University Hospital, Bordeaux, France; Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France.

Céleste Lebbe (C)

Department of Dermatology, APHP Dermatology, Paris 7 Diderot University, INSERM U976, Hôpital Saint-Louis, Paris, France; Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France.

Joseph Ciccolini (J)

SMARTc Unit, CRCM Inserm U1068, Aix Marseille Univ and APHM, Marseille, France; Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France.

David Combarel (D)

Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France; Service de Pharmacocinétique, Faculté de Pharmacie, Université Paris-Saclay, Châtenay-Malabry, 92 296, France.

Nicolas Meyer (N)

Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France; Université Paul Sabatier-Toulouse III, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche 1037-CRCT, Toulouse, France.

Angelo Paci (A)

Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France; Service de Pharmacocinétique, Faculté de Pharmacie, Université Paris-Saclay, Châtenay-Malabry, 92 296, France.

Stéphane Bouchet (S)

Service de Pharmacologie, Département de Biologie et Pathologie médicales, Gustave Roussy, Villejuif, 94805, France; Département de Pharmacologie, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France. Electronic address: stephane.bouchet@chu-bordeaux.fr.

Classifications MeSH