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ID 70822
フルテキストURL
著者
Shimizu, Junichi Department of Thoracic Oncology, Aichi Cancer Center Hospital
Nishio, Makoto Department of Thoracic Medical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Ohashi, Kadoaki Department of Respiratory Medicine, Okayama University Hospital ORCID Kaken ID researchmap
Osoegawa, Atsushi Department of Thoracic and Breast Surgery, Oita University Faculty of Medicine
Kikuchi, Eiki Department of Respiratory Medicine, Faculty of Medicine, Hokkaido University
Kimura, Hideharu Department of Respiratory Medicine, Kanazawa University Hospital
Goto, Yasushi Department of Thoracic Oncology, National Cancer Center Hospital
Miyauchi, Eisaku Department of Respiratory Medicine, Tohoku University Hospital
Yoshioka, Hiroshige Department of Thoracic Oncology, Kansai Medical University
Yoshino, Ichiro International University of Health and Welfare Narita Hospital
Misumi, Toshihiro Department of Data Science, National Cancer Center Hospital East
Yoshimori, Kozo Department of Clinical Oncology, Japan Anti‐Tuberculosis Association, Fukujuji Hospital
Shibata, Kazuhiko Department of Medical Oncology, Kouseiren Takaoka Hospital
Tsuda, Takeshi Division of Respiratory Medicine, Toyama Prefectural Central Hospital
Seike, Masahiro Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School
Ota, Takahiro Department of Respiratory Medicine, Kyoto City Hospital
Samata, Koichi Chugai Pharmaceutical Co., Ltd.
Kobayashi, Yuki Chugai Pharmaceutical Co., Ltd.
Tanaka, Misa Chugai Pharmaceutical Co., Ltd.
Gemma, Akihiko Nippon Medical School
抄録
Pivotal phase 3 trials leading to the approvals of atezolizumab─chemotherapy combinations for non-small cell and extensive-stage small cell lung cancer (NSCLC and ES-SCLC) had strict eligibility criteria. J-TAIL-2 was a prospective, observational study in Japan that evaluated atezolizumab regimens for advanced NSCLC/ES-SCLC, including patients ineligible for global trials. The primary endpoint was 12-month overall survival (OS); safety and efficacy in subgroups defined by age, ECOG PS and/or G8 score, and creatinine clearance were key secondary endpoints. As of February 3, 2023, 1217 patients were treated in clinical practice based on Japanese labeling/treatment guidelines. Patients received atezolizumab with either carboplatin and nab-paclitaxel (atezo + CnP), carboplatin/cisplatin and pemetrexed (atezo + PP), or bevacizumab and carboplatin and paclitaxel (atezo + bev + CP) in the NSCLC cohort (n = 814) or with carboplatin and etoposide (atezo + CE) in the ES-SCLC cohort (n = 403). Overall, 53.5% were ≥ 70 years old, and 11.8% had ECOG PS ≥ 2; median G8 scores were 13 (NSCLC cohort) and 12 (ES-SCLC). Patients < 70 and ≥ 70 years had similar median (m)OS and progression-free survival (mPFS) across treatment regimens. Patients with ECOG PS < 2 and G8 score ≥ median had the highest mOS/PFS vs. patients with ECOG PS ≥ 2 and G8 score
キーワード
atezolizumab
chemotherapy
non-small cell lung cancer
older
small cell lung cancer
発行日
2026-05-14
出版物タイトル
Cancer Science
出版者
Wiley
開始ページ
1
終了ページ
13
ISSN
1347-9032
NCID
AA11808050
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
© 2026 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1111/cas.70411
ライセンス
http://creativecommons.org/licenses/by-nc-nd/4.0/
Citation
J. Shimizu, M. Nishio, K. Ohashi, et al., “Atezolizumab + Chemotherapy in Older Patients With Lung Cancer in Japan,” Cancer Science (2026): 1–13, https://doi.org/10.1111/cas.70411.
助成情報
( 中外製薬株式会社 / Chugai Pharmaceutical Co. Ltd. )