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Prognostic Significance of 18F-FDG PET/CT and Tumor Metabolic Changes in Patients With Pancreatic Ductal Adenocarcinoma

  • Ayaka Shimomura
  • , Minoru Oshima
  • , Hironobu Suto
  • , Hiroyuki Matsukawa
  • , Akihiro Kondo
  • , Yasuhisa Ando
  • , Takayoshi Kishino
  • , Kensuke Kumamoto
  • , Kiyotoshi Sato
  • , Masahiro Sugimoto
  • , Mina Nagao
  • , Nobuyuki Miyatake
  • , Takashi Norikane
  • , Tomoyoshi Soga
  • , Keiichi Okano

Research output: Contribution to journalArticlepeer-review

Abstract

Background/Aim: 18F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) is reportedly associated with the malignant potential of cancer. This study aimed to evaluate the association between FDG accumulation and tumor metabolism in pancreatic ductal adenocarcinoma (PDAC). Patients and Methods: A prognostic analysis of data from 131 patients with PDAC who underwent FDG-PET/CT before curative-intent pancreatic surgery was performed. Capillary electrophoresis-mass spectrometry (CE-MS) was used to analyze the metabolome of tumor and non-neoplastic pancreas from 80 patients. These patients were divided into two groups: low SUVmax group (SUVmax <6.09) and high SUVmax group (SUVmax ≥6.09). Results: Carbohydrate antigen 19-9 (CA19-9), maximum standardized uptake value (SUVmax) of PET, N stage, and postoperative chemotherapy were identified as significant prognostic factors by univariate analysis. SUVmax emerged as an independent prognostic factor for overall survival [hazard ratio (HR)=1.88, p<0.05] and disease-free survival (HR=2.01, p<0.05) in multivariate analysis. Metabolic analyses confirmed that 43 metabolites significantly differed depending on the accumulation of SUV in tumors. Metabolites involved in the removal of reactive oxygen species (e.g., hypotaurine, glutathione, Met), treatment resistance (UDP-N-acetylglucosamine), and proliferation (e.g., choline, leucine, isoleucine) were increased in the high SUVmax group. Conclusion: FDG accumulation is an important independent prognostic factor reflecting tumor activity associated with metabolic changes in cancer cells.

Original languageEnglish
Pages (from-to)3321-3330
Number of pages10
JournalAnticancer research
Volume44
Issue number8
DOIs
Publication statusPublished - 2024 Aug

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CE-MS
  • FDG-PET
  • Metabolomics
  • PDAC
  • SUVmax

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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