Role of Pharmacogenetics in the Treatment of Acute Myeloid Leukemia: Systematic Review and Future Perspectives.

BCL2 inhibitors CD33 inhibitors FLT3 inhibitors IDH inhibitors acute myeloid leukemia anthracyclines cytarabine hypomethylating agents pharmacogenetics

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
03 Mar 2022
Historique:
received: 21 01 2022
revised: 16 02 2022
accepted: 28 02 2022
entrez: 26 3 2022
pubmed: 27 3 2022
medline: 27 3 2022
Statut: epublish

Résumé

Acute myeloid leukemia (AML) is a heterogeneous disease characterized by remarkable toxicity and great variability in response to treatment. Plenteous pharmacogenetic studies have already been published for classical therapies, such as cytarabine or anthracyclines, but such studies remain scarce for newer drugs. There is evidence of the relevance of polymorphisms in response to treatment, although most studies have limitations in terms of cohort size or standardization of results. The different responses associated with genetic variability include both increased drug efficacy and toxicity and decreased response or resistance to treatment. A broad pharmacogenetic understanding may be useful in the design of dosing strategies and treatment guidelines. The aim of this study is to perform a review of the available publications and evidence related to the pharmacogenetics of AML, compiling those studies that may be useful in optimizing drug administration.

Identifiants

pubmed: 35335935
pii: pharmaceutics14030559
doi: 10.3390/pharmaceutics14030559
pmc: PMC8954545
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Instituto de Salud Carlos III
ID : CD21/00022
Organisme : Instituto de Salud Carlos III
ID : IMPaCT, IMP/00009

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Auteurs

Álvaro Pinto-Merino (Á)

Department of Health Sciences, University of Burgos, 09001 Burgos, Spain.

Jorge Labrador (J)

Research Unit, Fundación Burgos por la Investigación de la Salud (FBIS), Hospital Universitario de Burgos, 09006 Burgos, Spain.
Haematology Department, Hospital Universitario de Burgos, 09006 Burgos, Spain.
Facultad de Ciencias de la Salud, Universidad Isabel I, 09003 Burgos, Spain.

Pablo Zubiaur (P)

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), 28029 Madrid, Spain.
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.

Raquel Alcaraz (R)

Research Unit, Fundación Burgos por la Investigación de la Salud (FBIS), Hospital Universitario de Burgos, 09006 Burgos, Spain.

María José Herrero (MJ)

Pharmacogenetics Department, Hospital Universitari i Politècnic La Fe, 46026 Valencia, Spain.

Pau Montesinos (P)

Haematology Department, Hospital Universitari i Politècnic La Fe, 46026 Valencia, Spain.

Francisco Abad-Santos (F)

Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), 28029 Madrid, Spain.
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.

Miriam Saiz-Rodríguez (M)

Department of Health Sciences, University of Burgos, 09001 Burgos, Spain.
Research Unit, Fundación Burgos por la Investigación de la Salud (FBIS), Hospital Universitario de Burgos, 09006 Burgos, Spain.

Classifications MeSH