ID | 69117 |
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Soh, Junichi
Department of Thoracic Surgery, Okayama University Hospital
Yamamoto, Hiromasa
Department of Thoracic Surgery, Okayama University Hospital
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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
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Hotta, Katsuyuki
Center for Innovative Clinical Medicine, Okayama University Hospital
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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
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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.
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Keywords | non‑small cell lung cancer
elderly patients
adjuvant chemotherapy
S‑1
EGFR
TP
TS
OPRT
ERCC1
DPD
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Published Date | 2025-07-03
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Publication Title |
Molecular and Clinical Oncology
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Volume | volume23
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Issue | issue3
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Publisher | Spandidos Publications
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Start Page | 79
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ISSN | 2049-9450
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Content Type |
Journal Article
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language |
English
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OAI-PMH Set |
岡山大学
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Copyright Holders | © Soh et al.
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File Version | publisher
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PubMed ID | |
DOI | |
Web of Science KeyUT | |
Related Url | isVersionOf https://doi.org/10.3892/mco.2025.2874
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License | https://creativecommons.org/licenses/by-nc-nd/4.0/
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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.
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