| ID | 70822 |
| FullText URL | |
| Author |
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
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| Abstract | 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 |
| Keywords | atezolizumab
chemotherapy
non-small cell lung cancer
older
small cell lung cancer
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| Published Date | 2026-05-14
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| Publication Title |
Cancer Science
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| Publisher | Wiley
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| Start Page | 1
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| End Page | 13
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| ISSN | 1347-9032
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| NCID | AA11808050
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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 | © 2026 The Author(s).
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| File Version | publisher
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| PubMed ID | |
| DOI | |
| Web of Science KeyUT | |
| Related Url | isVersionOf https://doi.org/10.1111/cas.70411
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| License | http://creativecommons.org/licenses/by-nc-nd/4.0/
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| 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.
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| 助成情報 |
( 中外製薬株式会社 / Chugai Pharmaceutical Co. Ltd. )
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