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ID 65896
フルテキストURL
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著者
Yamamoto, Hiromasa Department of Thoracic Surgery, Okayama University Hospital ORCID Kaken ID publons researchmap
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 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
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
出版物タイトル
PLoS ONE
18巻
5号
出版者
Public Library of Science
開始ページ
e0285273
ISSN
1932-6203
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2023 Yamamoto et al.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1371/journal.pone.0285273
ライセンス
https://creativecommons.org/licenses/by/4.0/
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