Genotype-based chemotherapy for patients with gastrointestinal tumors: focus on oxaliplatin, irinotecan, and fluoropyrimidines

Drug Metab Pers Ther. 2021 Nov 30;37(3):223-228. doi: 10.1515/dmpt-2021-0162. eCollection 2022 Sep 1.

Abstract

This review aimed to summarize the pharmacogenetic studies of the most commonly used drugs in the chemotherapy of gastrointestinal (GI) tumors: oxaliplatin, irinotecan, and fluoropyrimidines. So far, it has not been possible to develop an effective genotype-based approach for oxaliplatin. More and more evidence is emerging in favor of the fact that the choice of a dose of fluorouracil based on pharmacogenetic testing according to DPYD*2A, can be not only effective but also cost-effective. Additional, well-planned trials of the UGT1A1 genotype-based approach to irinotecan therapy are predicted to reduce adverse drug events in people with the UGT1A1*28/*28 genotypes and improve treatment efficacy in the rest of the patients, which might be cost-effective.

Keywords: GSTM1; GSTT1; UGT1A1; dihydropyrimidine dehydrogenase (DPYD); excision repair and cross-complementation (ERCC); fluoropyrimidines; irinotecan; oxaliplatin.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fluorouracil / adverse effects
  • Gastrointestinal Neoplasms* / chemically induced
  • Gastrointestinal Neoplasms* / drug therapy
  • Gastrointestinal Neoplasms* / genetics
  • Genotype
  • Humans
  • Irinotecan / therapeutic use
  • Oxaliplatin / therapeutic use

Substances

  • Oxaliplatin
  • Irinotecan
  • Fluorouracil