| Literature DB >> 27381050 |
Juan Eduardo Megías-Vericat1,2, Pau Montesinos3, María José Herrero1,4, Virginia Bosó1,2, David Martínez-Cuadrón3, José Luis Poveda2, Miguel Ángel Sanz3, Salvador F Aliño1,4,5.
Abstract
Acute myeloid leukemia (AML) is a clinically and biologically heterogeneous malignancy that is primarily treated with combinations of cytarabine and anthracyclines. Although this scheme remains effective in most of the patients, variability of outcomes in patients has been partly related with their genetic variability. Several pharmacogenetic studies have analyzed the impact of polymorphisms in genes encoding transporters, metabolizers or molecular targets of chemotherapy agents. A systematic review on all eligible studies was carried out in order to estimate the effect of polymorphisms of anthracyclines and cytarabine pathways on efficacy and toxicity of AML treatment. Other emerging genes recently studied in AML, such as DNA repair genes, genes potentially related to chemotherapy response or AML prognosis, have also been included.Entities:
Keywords: SNP; acute myeloid leukemia; anthracyclines; cytarabine; effectiveness; polymorphism; toxicity
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Year: 2016 PMID: 27381050 DOI: 10.2217/pgs-2016-0055
Source DB: PubMed Journal: Pharmacogenomics ISSN: 1462-2416 Impact factor: 2.533