5-Fluorouracil metabolic pathway genes predict recurrence risk following adjuvant S-1 therapy: Results of an ancillary analysis from a phase III trial of resected biliary tract cancer (JCOG1202A1)

J Hepatobiliary Pancreat Sci. 2024 Dec;31(12):886-896. doi: 10.1002/jhbp.12071. Epub 2024 Sep 25.

Abstract

Background: S-1, an oral fluoropyrimidine derivative, is standard adjuvant therapy for resected biliary tract cancer (BTC), based on the results of the JCOG1202, a phase III trial evaluating the survival benefit with adjuvant S-1 following curative resection for BTC compared to surgery alone. This multicenter ancillary study of the JCOG1202 aimed to evaluate the prognostic impact of the 5-fluorouracil (5-FU) metabolic pathway genes including thymidine phosphorylase (TP) and dihydropyrimidine dehydrogenase (DPD).

Methods: The 5-FU metabolic pathway genes were measured in tumor cells from formalin-fixed paraffin-embedded resected specimens from 183 patients (surgery alone: n = 94; adjuvant S-1: n = 89). We randomly divided them into training (n = 96) and validation sets (n = 87) for evaluating the interaction between gene levels and RFS benefits in the treatment arm.

Results: RFS benefits of adjuvant S-1 were observed in the low DPD (HR = 0.440 and 0.748, respectively in the training and validation sets) and the low TP groups (HR = 0.709 and 0.602, respectively). Clinicopathological characteristics were well balanced between low and high DPD populations. More advanced stage tumors were observed in high TP populations as compared to those in low TP populations (p = .0332).

Conclusion: The results suggest the RFS benefit of adjuvant S-1 in resected BTC patients with low DPD and low TP gene expressions.

Keywords: 5‐FU metabolic pathway; DPD; S‐1; adjuvant; biliary tract cancer.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Antimetabolites, Antineoplastic* / therapeutic use
  • Biliary Tract Neoplasms* / drug therapy
  • Biliary Tract Neoplasms* / genetics
  • Biliary Tract Neoplasms* / metabolism
  • Biliary Tract Neoplasms* / pathology
  • Biliary Tract Neoplasms* / surgery
  • Chemotherapy, Adjuvant
  • Dihydrouracil Dehydrogenase (NADP) / genetics
  • Dihydrouracil Dehydrogenase (NADP) / metabolism
  • Drug Combinations*
  • Female
  • Fluorouracil* / therapeutic use
  • Humans
  • Male
  • Metabolic Networks and Pathways / genetics
  • Middle Aged
  • Neoplasm Recurrence, Local* / genetics
  • Oxonic Acid* / therapeutic use
  • Prognosis
  • Risk Assessment
  • Tegafur* / therapeutic use
  • Thymidine Phosphorylase / genetics
  • Thymidine Phosphorylase / metabolism

Substances

  • Tegafur
  • Oxonic Acid
  • S 1 (combination)
  • Fluorouracil
  • Antimetabolites, Antineoplastic
  • Drug Combinations
  • Dihydrouracil Dehydrogenase (NADP)
  • Thymidine Phosphorylase