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DNA variants in DHFR gene and response to treatment in children with childhood B ALL: Revisited in AIEOP-BFM protocol

Authors :
Maja Krajinovic
Laurance Douyon
Vincent Gagné
Barbara Buldini
Camille J Quintin
Giovanni Cazzaniga
Giuseppe Basso
Francesco Ceppi
Rosanna Parasole
Antonella Colombini
Valentino Conter
Ceppi, F
Gagné, V
Douyon, L
Quintin, C
Colombini, A
Parasole, R
Buldini, B
Basso, G
Conter, V
Cazzaniga, G
Krajinovic, M
Publication Year :
2018
Publisher :
Future Medicine Ltd., 2018.

Abstract

Aim: We have previously reported an association of dihydrofolate reductase promoter polymorphisms with reduced event-free survival in childhood acute lymphoblastic leukemia (ALL) patients treated with Dana Farber Cancer Institute protocol. Here, we assessed whether these associations are applicable to other protocol, based on different methotrexate doses. Methods: Genotypes for six tag polymorphisms and resulting haplotypes were analyzed for an association with ALL outcome. Results: The association was found with the polymorphisms A-680C, A-317G and C-35T in high-risk group patients. Carriers of haplotype *1 had a remarkably higher risk of events compared with noncarriers and a lower probability of event-free survival (21.4 vs 81.3%). Conclusion: The role of DHFR variants in predicting the outcome of childhood ALL extends beyond single-treatment protocol and can be useful biomarker in personalizing treatment.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....752449b810e2134f650df07bba094b14