ID | 68724 |
JaLCDOI | |
フルテキストURL | |
著者 |
Kanaji, Nobuhiro
Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine, Faculty of Medicine, Kagawa University
Nishii, Kazuya
Department of Respiratory Medicine, National Hospital Organization Iwakuni Clinical Center
Tsubata, Yukari
Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine
Nakao, Mika
Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine
Okuno, Takae
Department of Internal Medicine, Division of Medical Oncology and Respiratory Medicine, Shimane University Faculty of Medicine
Okawa, Sachi
Department of Allergy and Respiratory Medicine, Okayama University Hospital
Takata, Kenji
Department of Allergy and Respiratory Medicine, Okayama University Hospital
Kodani, Masahiro
Division of Medical Oncology and Molecular Respirology, Faculty of Medicine, Tottori University
Yamasaki, Masahiro
Department of Respiratory Disease, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital
Fujitaka, Kazunori
Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University
Kubota, Tetsuya
Department of Respiratory Medicine and Allergology, Kochi University
Inoue, Masaaki
Department of Chest Surgery, Shimonoseki City Hospital
Watanabe, Naoki
Department of Internal Medicine, Division of Hematology, Rheumatology and Respiratory Medicine, Faculty of Medicine, Kagawa University
Hotta, Katsuyuki
Center for Innovative Clinical Medicine, Okayama University Hospital
CS-Lung-003 Investigator
|
抄録 | This prospective observational study investigated the clinical status of patients with advanced non-small cell lung cancer (NSCLC) treated with cytotoxic chemotherapy+an immune checkpoint inhibitor (chemo + IO) as first-line treatment in a real-world setting. The cases of 98 patients treated with chemo + IO were prospectively collected and analyzed for effectiveness and safety. The response rate to chemo + IO was 46.9%, and the disease control rate was 76.5%. The median progression-free survival and overall survival (OS) in the total population were 5.2 and 22.3 months, respectively. The patients positive for PD-L1 (≥ 1%) showed significantly longer OS than the negative group (<1%) (median 26.7 vs. 18.7 months, p=0.04). Pre-existing interstitial lung disease (ILD) was associated with shorter OS than the absence of ILD (median 9.0 vs. 22.6 months, p<0.01). Immunerelated adverse events (irAEs) were observed in 28 patients (28.6%). The most frequent irAE was ILD (n=11); Grade 1 (n=1 patient), G2 (n=5), G3 (n=4), and only a single patient with a G5 irAE. In this CS-Lung-003 study, first-line chemo + IO in a real-world setting showed good effectiveness, comparable to that observed in international clinical trials. In real-world practice, chemo + IO is a promising and steadfast strategy.
|
キーワード | non-small cell lung cancer
real-world
first-line
immune checkpoint inhibitor
combined immunotherapy
|
Amo Type | Original Article
|
出版物タイトル |
Acta Medica Okayama
|
発行日 | 2025-06
|
巻 | 79巻
|
号 | 3号
|
出版者 | Okayama University Medical School
|
開始ページ | 167
|
終了ページ | 176
|
ISSN | 0386-300X
|
NCID | AA00508441
|
資料タイプ |
学術雑誌論文
|
言語 |
英語
|
著作権者 | Copyright Ⓒ 2025 by Okayama University Medical School
|
論文のバージョン | publisher
|
査読 |
有り
|