Role of pharmacogenetics on deferasirox AUC and efficacy

Pharmacogenomics. 2016 Apr;17(6):561-72. doi: 10.2217/pgs-2015-0001. Epub 2016 Apr 4.

Abstract

Aim: We evaluated deferasirox pharmacokinetic according to SNPs in genes involved in its metabolism and elimination. Moreover, we defined a plasma area under the curve cut-off value predicting therapy response.

Patients & methods: Allelic discrimination was performed by real-time PCR. Drug plasma concentrations were measured by a high performance liquid chromatography system coupled with an ultraviolet method.

Results: Pharmacokinetic parameters were significantly influenced by UGT1A1 rs887829C>T, UGT1A3 rs1983023C>T and rs3806596A>G SNPs. Area under the curve cut-off values of 360 μg/ml/h for efficacy were here defined and 250 μg/ml/h for nonresponse was reported. UGT1A3 rs3806596GG and ABCG2 rs13120400CC genotypes were factors able to predict efficacy, whereas UGT1A3 rs3806596GG was a nonresponse predictor.

Conclusion: These data show how screening patient's genetic profile may help clinicians to optimize iron chelation therapy with deferasirox.

Keywords: ABCG2; SNPs; UGT1A1; UGT1A3; iron overload; pharmacokinetics.

MeSH terms

  • Adult
  • Alleles
  • Area Under Curve
  • Benzoates / blood*
  • Benzoates / pharmacokinetics*
  • Cohort Studies
  • Deferasirox
  • Female
  • Genotype
  • Glucuronosyltransferase / genetics
  • Humans
  • Male
  • Pharmacogenetics / methods
  • Polymorphism, Single Nucleotide / genetics*
  • Triazoles / blood*
  • Triazoles / pharmacokinetics*

Substances

  • Benzoates
  • Triazoles
  • UDP-glucuronosyltransferase, UGT1A3
  • UGT1A1 enzyme
  • Glucuronosyltransferase
  • Deferasirox