4.2 Article

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

Journal

PHARMACOGENOMICS
Volume 19, Issue 2, Pages 105-112

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/pgs-2017-0153

Keywords

childhood ALL; dihydrofolate reductase polymorphisms; treatment outcome

Funding

  1. Leukemia Lymphoma Society of Canada
  2. Charles Bruneau Foundation
  3. Associazione Italiana per la Ricerca sul Cancro

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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.

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