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Author
Soh, Junichi Department of Thoracic Surgery, Okayama University Hospital
Yamamoto, Hiromasa Department of Thoracic Surgery, Okayama University Hospital ORCID Kaken ID publons researchmap
Okumura, Norihito Department of Thoracic Surgery, Kurashiki Central Hospital
Suzuki, Hiroyuki Department of Chest Surgery, Fukushima Medical University Hospital
Nakata, Masao Department of General Thoracic Surgery, Kawasaki Medical School Hospital
Fujiwara, Toshiya Department of Thoracic Surgery, Hiroshima City Hiroshima Citizens Hospital
Gemba, Kenicehi Department of Respiratory Medicine, Chugoku Central Hospital, Fukuyama, Hiroshima 720‑0001, Japan; 8Department of Respiratory Surgery, Japanese Red Cross Nagasaki Genbaku Hospital
Sano, Isao Department of Respiratory Surgery, Japanese Red Cross Nagasaki Genbaku Hospital
Fujinaga, Takuji Department of General Thoracic Surgery, National Hospital Organization Nagara Medical Center
Kataoka, Masafumi Department of Surgery and Respiratory Center, Okayama Saiseikai General Hospital
Terasaki, Yasuhiro Department of Respiratory Surgery, Saga Medical Center Koseikan
Fujimoto, Nobukazu Department of Medical Oncology and Respiratory Medicine, Okayama Rosai Hospital
Kataoka, Kazuhiko Department of Thoracic Surgery, National Hospital Organization Iwakuni Clinical Center
Kosaka, Shinji Department of Thoracic Surgery, Shimane Prefectural Central Hospital
Yamashita, Motohiro Department of Thoracic Surgery, National Hospital Organization Shikoku Cancer Center
Inokawa, Hidetoshi Department of Thoracic Surgery, National Hospital Organization Yamaguchi‑Ube Medical Center
Inoue, Masaaki Department of Thoracic Surgery, Shimonoseki City Hospital
Nakamura, Hiroshige Division of General Thoracic Surgery, Tottori University Hospital
Yamashita, Yoshinori Department of Thoracic Surgery, National Hospital Organization Kure Medical Center and Chugoku Cancer Center
Takahashi, Yuta Department of Thoracic Surgery, Okayama University Hospital
Torigoe, Hidejiro Department of Thoracic Surgery, Okayama University Hospital
Sato, Hiroki Department of Thoracic Surgery, Okayama University Hospital
Tomida, Shuta Center for Comprehensive Genomic Medicine, Okayama University Hospital Kaken ID researchmap
Hotta, Katsuyuki Center for Innovative Clinical Medicine, Okayama University Hospital Kaken ID publons researchmap
Yoshioka, Hiroshige Department of Thoracic Oncology, Kansai Medical University Hospital
Morita, Satoshi Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine
Matsuo, Keitaro Division of Cancer Epidemiology and Prevention, Aichi Cancer Center Research Institute
Sakamoto, Junichi Tokai Central Hospital
Date, Hiroshi Department of Thoracic Surgery, Kyoto University Hospital
Toyooka, Shinichi Department of Thoracic Surgery, Okayama University Hospital ORCID Kaken ID publons researchmap
Abstract
Managing elderly patients presents several challenges because of age‑related declines; however, age should not be the sole determinant for adjuvant treatment decisions in patients with non‑small cell lung cancer (NSCLC). Moreover, age may affect the expression of 5‑fluorouracil (5‑FU) biomarkers. The present study assessed: i) The effect of age on the expression levels of 5‑FU biomarkers by analyzing a public database; and ii) the ability of these biomarkers to predict clinical outcomes in elderly patients with NSCLC who underwent complete resection in the Setouchi Lung Cancer Group Study 1201 (SCLG1201) followed by S‑1 adjuvant chemotherapy. Changes in gene expression levels across age groups were assessed by analyzing The Cancer Genome Atlas (TCGA) database. The expression of 5‑FU biomarkers, including thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD), orotate phosphoribosyltransferase, epidermal growth factor receptor (EGFR) and excision repair cross‑complementation group 1 (ERCC1), were assessed via quantitative reverse‑transcription PCR assays in 89 elderly patients (≥75 years) with NSCLC who received adjuvant chemotherapy with oral fluoropyrimidine prodrug S‑1 in the SLCG1201 trial. TCGA database analysis (n=955) showed that TS expression decreased significantly with aging, especially in the age group ≥75. In the SCLG1201 trial, univariate analysis revealed that EGFR upregulation and TS downregulation were correlated with favorable recurrence‑free survival (RFS) and overall survival (OS), respectively. Multivariate analysis demonstrated that pathological stage was an independent prognostic factor for both RFS and OS. EGFR mutations were associated with upregulation of DPD and EGFR, and downregulation of TS and ERCC1. In conclusion, although pathological stage is an independent prognostic factor for survival, EGFR upregulation and TS downregulation may be a greater predictor of clinical outcomes in elderly patients with NSCLC treated with S‑1 adjuvant chemotherapy. The age‑related decrease in TS expression supports the potential benefit of 5‑FU therapies in elderly patients. Nonetheless, further research is warranted to validate these results.
Keywords
non‑small cell lung cancer
elderly patients
adjuvant chemotherapy
S‑1
EGFR
TP
TS
OPRT
ERCC1
DPD
Published Date
2025-07-03
Publication Title
Molecular and Clinical Oncology
Volume
volume23
Issue
issue3
Publisher
Spandidos Publications
Start Page
79
ISSN
2049-9450
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© Soh et al.
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publisher
PubMed ID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.3892/mco.2025.2874
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Citation
Soh J, Yamamoto H, Okumura N, Suzuki H, Nakata M, Fujiwara T, Gemba K, Sano I, Fujinaga T, Kataoka M, Kataoka M, et al: Association of the expression of 5‑FU biomarkers with aging and prognosis in elderly patients with lung cancer treated with S‑1 adjuvant chemotherapy: Follow‑up results of the Setouchi Lung Cancer Group Study 1201. Mol Clin Oncol 23: 79, 2025.