ID | 65896 |
フルテキストURL | |
著者 |
Yamamoto, Hiromasa
Department of Thoracic Surgery, Okayama University Hospital
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Soh, Junichi
Department of Surgery, Division of Thoracic Surgery, Kindai University Faculty of Medicine
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, Kenichi
Department of Respiratory Medicine, Chugoku Central 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
Terazaki, Yasuhiro
Department of Respiratory S0urgery, Saga-Ken Medical Centre 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 Chest 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
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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抄録 | Background
It is shown that the postoperative adjuvant chemotherapy for non-small cell lung cancer (NSCLC) was associated with survival benefit in an elderly population. We aimed to analyze the feasibility and efficacy of alternate-day S-1, an oral fluoropyrimidine, for adjuvant chemotherapy in elderly patients with completely resected pathological stage IA (tumor diameter > 2 cm) to IIIA (UICC TNM Classification of Malignant Tumours, 7th edition) NSCLC. Methods Elderly patients were randomly assigned to receive adjuvant chemotherapy for one year consisting of either alternate-day oral administration of S-1 (80 mg/m2/day) for 4 days a week (Arm A) or a daily oral administration of S-1 (80 mg/m2/day) for 14 consecutive days followed by 7-day rest (Arm B). The primary endpoint was feasibility (treatment completion rate), which was defined as the proportion of patients who completed the allocated intervention for 6 months with a relative dose intensity (RDI) of 70% or more. Results We enrolled 101 patients in which 97 patients received S-1 treatment. The treatment completion rate at 6 months was 69.4% in Arm A and 64.6% in Arm B (p = 0.67). Treatment completion rate in Arm B tended to be lower compared to Arm A, as the treatment period becomes longer (at 9 and 12 months). RDI of S-1 at 12 months and completion of S-1 administration without dose reduction or postponement at 12 months was significantly better in Arm A than in Arm B (p = 0.026 and p < 0.001, respectively). Among adverse events, anorexia, skin symptoms and lacrimation of any grade were significantly more frequent in Arm B compared with Arm A (p = 0.0036, 0.023 and 0.031, respectively). The 5-year recurrence-free survival rates were 56.9% and 65.7% for Arm A and B, respectively (p = 0.22). The 5-year overall survival rates were 68.6% and 82.0% for Arm A and B, respectively (p = 0.11). Conclusion Although several adverse effects were less frequent in Arm A, both alternate-day and daily oral administrations of S-1 were demonstrated to be feasible in elderly patients with completely resected NSCLC. |
発行日 | 2023-05-19
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出版物タイトル |
PLoS ONE
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巻 | 18巻
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号 | 5号
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出版者 | Public Library of Science
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開始ページ | e0285273
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ISSN | 1932-6203
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資料タイプ |
学術雑誌論文
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言語 |
英語
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OAI-PMH Set |
岡山大学
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著作権者 | © 2023 Yamamoto et al.
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論文のバージョン | publisher
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PubMed ID | |
DOI | |
Web of Science KeyUT | |
関連URL | isVersionOf https://doi.org/10.1371/journal.pone.0285273
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ライセンス | https://creativecommons.org/licenses/by/4.0/
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Citation | Yamamoto H, Soh J, Okumura N, Suzuki H, Nakata M, Fujiwara T, et al. (2023) Randomized phase II study of daily versus alternate-day administrations of S-1 for the elderly patients with completely resected pathological stage IA (tumor diameter > 2 cm)—IIIA of non-small cell lung cancer: Setouchi Lung Cancer Group Study 1201. PLoS ONE 18(5): e0285273. https://doi.org/ 10.1371/journal.pone.0285273
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