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PERSONALIZATION OF 6-MERCAPTOPURINE THERAPY FOR CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA
  1. Goran Milošević1,
  2. Lidija Dokmanović1,
  3. Nada Krstovski1,
  4. Jelena Lazić1,
  5. Predrag Rodić1,
  6. Sonja Pavlović2,
  7. Branka Zukić2,
  8. Nikola Kotur2,
  9. Dragana Janić1
  1. 1University Children's Hospital, Belgrade
  2. 2Institute of molecular genetics and genetic engineering, University of Belgrade

Abstract

Introduction Treatment of acute lymphoblastic leukemia (ALL) in children has been significantly improved over past few decades. Optimal use of known antileukemic drugs has lead to four-fold increase of overall survival. Nevertheless, therapy failure occurs in 15–20% of patients. Individualized use of cytostatic drugs can help us reducing toxicity-related deaths and improve therapy outcome.

Materials and methods We studied multidrug resistance protein 4 gene (ABCC4) and inosin triphosphate pyrophosphatase (ITPA) gene polymorphisms to assess their influence on occurrence and intensity of 6-MP toxicity during maintenance phase of ALL treatment in children as well as on treatment outcome.

Results Thiopurine S-methyltransferase (TPMT) genotype was known for all patients before start of therapy and doses were adjusted accordingly. Five patients (7%) were carriers of ITPAc.94C>A genotype. Heterozygote and homozygote carriers of variant alleles for ABCC4 rs9516519 T>G, genotype were represented in 35% and 4% of our patients, respectively. We did not show correlation of variant alleles with increased number of off-therapy weeks neither with number of episodes of leukopenia. Cross-validated AUC for each of genetic markers individually showed low predictive power (cross-validated AUC around 0.5) for predicting toxicity. However, combination of two genetic markers and known TPMT gentotype improved the predictability (cross-validated AUC was 0.65).

Conclusions Our results did not show correlation with toxicity using individual genetic markers. However, in the settings of known TPMT genotype, we showed the potential of using all three genetic markers (including TPMT) in predicting who might be in danger of having increased toxicity.

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