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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
Abstract
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.
Keywords
non-small cell lung cancer
real-world
first-line
immune checkpoint inhibitor
combined immunotherapy
Amo Type
Original Article
Publication Title
Acta Medica Okayama
Published Date
2025-06
Volume
volume79
Issue
issue3
Publisher
Okayama University Medical School
Start Page
167
End Page
176
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
Copyright Ⓒ 2025 by Okayama University Medical School
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publisher
Refereed
True