Pharmacokinetics and pharmacodynamics of approved monoclonal antibody therapy for colorectal cancer.


Journal

Expert opinion on drug metabolism & toxicology
ISSN: 1744-7607
Titre abrégé: Expert Opin Drug Metab Toxicol
Pays: England
ID NLM: 101228422

Informations de publication

Date de publication:
Nov 2022
Historique:
pubmed: 31 12 2022
medline: 14 1 2023
entrez: 30 12 2022
Statut: ppublish

Résumé

The introduction of monoclonal antibodies to the chemotherapy backbone treatment has challenged the paradigm of metastatic colorectal cancer (mCRC) treatment. Their mechanism of action and pharmacokinetics are complex but important to understand in order to improve patient selection and treatment outcomes for mCRC population. This review examines the scientific data, pharmacodynamics, and pharmacokinetics of approved monoclonal antibodies used to treat mCRC patients, including agents targeting signaling via VEGFR (bevacizumab and ramucirumab), EGFR (cetuximab and panitumumab), HER2/3 target therapy, and immunotherapy agents such as pembrolizumab or nivolumab. Efficacy and mechanism of action of bispecific antibodies are also covered. mCRC is a heterogeneous disease and the optimal selection and sequence of treatments is challenging. Monoclonal antibodies have complex pharmacokinetics and pharmacodynamics, with important interactions between them. The arrival of bioequivalent molecules to the market increases the need for the characterization of pharmacokinetics and pharmacodynamics of classic monoclonal antibodies to reach bioequivalent novel molecules.

Identifiants

pubmed: 36582117
doi: 10.1080/17425255.2022.2160316
doi:

Substances chimiques

Antineoplastic Agents 0
ErbB Receptors EC 2.7.10.1
Antibodies, Monoclonal 0
Cetuximab PQX0D8J21J

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

755-767

Auteurs

Nadia Saoudi Gonzalez (N)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Medical Oncology Department, Vall d'Hebron Institute of Oncology, Vhio Barcelona, Spain.

Daniel López (D)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.

Diego Gómez (D)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.

Javier Ros (J)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Medical Oncology Department, Vall d'Hebron Institute of Oncology, Vhio Barcelona, Spain.

Iosune Baraibar (I)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Medical Oncology Department, Vall d'Hebron Institute of Oncology, Vhio Barcelona, Spain.

Francesc Salva (F)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Medical Oncology Department, Vall d'Hebron Institute of Oncology, Vhio Barcelona, Spain.

Josep Tabernero (J)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Medical Oncology Department, Vall d'Hebron Institute of Oncology, Vhio Barcelona, Spain.

Elena Élez (E)

Medical Oncology Department, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Medical Oncology Department, Vall d'Hebron Institute of Oncology, Vhio Barcelona, Spain.

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Classifications MeSH