Cost-effectiveness of screening for DPYD polymorphisms to prevent neutropenia in cancer patients treated with fluoropyrimidines

Pharmacogenomics. 2016 Jun;17(9):979-84. doi: 10.2217/pgs-2016-0006. Epub 2016 Jun 1.

Abstract

Aim: To compare the cost of screening for three mutations in the dihydropyrimidine dehydrogenase gene and the costs of treating severe fluoropyrimidine-induced neutropenia.

Materials & methods: The polymorphisms rs3918290 (DPYD*2A), rs67376798 (DPYD 2846A>T) and rs55886062 (1679T>G, DPYD*13) were genotyped using real-time PCR, TaqMan probes and a rapid cell lysis to provide PCR-ready DNA.

Results: We found that genotyping 1000 patients in our center cost €6400 and that the mean cost of treating severe neutropenia was €3044. Therefore, if severe fluoropyrimidine-induced neutropenia is reduced by genotyping the three DPYD variations in at least 2.21 cases per 1000 treated patients, then DPYD genotyping will prove cost effective.

Conclusion: We demonstrated that real-time DPYD genotyping using TaqMan probes is cost effective in all fluoropyrimidine-based treatments.

Keywords: 5-fluorouracil; capecitabine; drug adverse reactions.

MeSH terms

  • Antimetabolites, Antineoplastic / adverse effects*
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Colorectal Neoplasms / genetics
  • Cost-Benefit Analysis
  • Dihydrouracil Dehydrogenase (NADP) / genetics*
  • Female
  • Fluorouracil / adverse effects*
  • Genetic Testing / economics*
  • Genotype
  • Humans
  • Male
  • Neoplasms / drug therapy*
  • Neoplasms / genetics*
  • Neutropenia / economics
  • Neutropenia / genetics*
  • Neutropenia / prevention & control*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics*

Substances

  • Antimetabolites, Antineoplastic
  • Dihydrouracil Dehydrogenase (NADP)
  • Fluorouracil