CDK4/6 Inhibitors in Breast Cancer Treatment: Potential Interactions with Drug, Gene, and Pathophysiological Conditions.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
01 Sep 2020
Historique:
received: 16 07 2020
revised: 11 08 2020
accepted: 26 08 2020
entrez: 5 9 2020
pubmed: 5 9 2020
medline: 30 3 2021
Statut: epublish

Résumé

Palbociclib, ribociclib, and abemaciclib belong to the third generation of cyclin-dependent kinases inhibitors (CDKis), an established therapeutic class for advanced and metastatic breast cancer. Interindividual variability in the therapeutic response of CDKis has been reported and some individuals may experience increased and unexpected toxicity. This narrative review aims at identifying the factors potentially concurring at this variability for driving the most appropriate and tailored use of CDKis in the clinic. Specifically, concomitant medications, pharmacogenetic profile, and pathophysiological conditions could influence absorption, distribution, metabolism, and elimination pharmacokinetics. A personalized therapeutic approach taking into consideration all factors potentially contributing to an altered pharmacokinetic/pharmacodynamic profile could better drive safe and effective clinical use.

Identifiants

pubmed: 32883002
pii: ijms21176350
doi: 10.3390/ijms21176350
pmc: PMC7504705
pii:
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Cyclin-Dependent Kinase 4 EC 2.7.11.22
Cyclin-Dependent Kinase 6 EC 2.7.11.22

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ministero della Salute
ID : [no grant number provided]

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Auteurs

Rossana Roncato (R)

Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.

Jacopo Angelini (J)

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.

Arianna Pani (A)

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Clinical Pharmacology Unit, ASST Grande Ospedale Metropolitano Niguarda, Piazza dell'Ospedale Maggiore 3, 20162 Milan, Italy.

Erika Cecchin (E)

Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.

Andrea Sartore-Bianchi (A)

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Department of Hematology and Oncology, Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, 20162 Milan, Italy.

Salvatore Siena (S)

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Department of Hematology and Oncology, Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, 20162 Milan, Italy.

Elena De Mattia (E)

Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.

Francesco Scaglione (F)

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Clinical Pharmacology Unit, ASST Grande Ospedale Metropolitano Niguarda, Piazza dell'Ospedale Maggiore 3, 20162 Milan, Italy.

Giuseppe Toffoli (G)

Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.

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