PLoS ONE (Jan 2014)

Thymidylate synthase genotype-directed chemotherapy for patients with gastric and gastroesophageal junction cancers.

  • Laura W Goff,
  • Nilay Thakkar,
  • Liping Du,
  • Emily Chan,
  • Benjamin R Tan,
  • Dana B Cardin,
  • Howard L McLeod,
  • Jordan D Berlin,
  • Barbara Zehnbauer,
  • Chloe Fournier,
  • Joel Picus,
  • Andrea Wang-Gillam,
  • Wooin Lee,
  • A Craig Lockhart

DOI
https://doi.org/10.1371/journal.pone.0107424
Journal volume & issue
Vol. 9, no. 9
p. e107424

Abstract

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Retrospective studies indicate associations between TSER (thymidylate synthase enhancer region) genotypes and clinical outcomes in patients receiving 5-FU based chemotherapy, but well-controlled prospective validation has been lacking.In this phase II study (NCT00515216 registered through ClinicalTrials.gov, http://clinicaltrials.gov/show/NCT00515216), patients with "good risk" TSER genotypes (at least one TSER*2 allele) were treated with FOLFOX chemotherapy to determine whether prospective patient selection can improve overall response rates (ORR) in patients with gastric and gastroesophageal junction (GEJ) cancers, compared with historical outcomes in unselected patients (estimated 43%).The ORR in genotype-selected patients was 39.1% (9 partial responses out of 23 evaluable patients, 95% CI, 22.2 to 59.2), not achieving the primary objective of improving ORR. An encouraging disease control rate (DCR, consisting of partial responses and stable diseases) of 95.7% was noted and patients with homozygous TSER*2 genotype showed better tumor response.In this first prospective, multi-institutional study in patients with gastric or GEJ cancers, selecting patients with at least one TSER*2 allele did not improve the ORR but led to an encouraging DCR. Further studies are needed to investigate the utility of selecting patients homozygous for the TSER*2 allele and additional genomic markers in improving clinical outcomes for patients with gastric and GEJ cancers.ClinicalTrials.gov NCT00515216.