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ID 69176
フルテキストURL
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著者
Dingemans, Anne-Marie C. Erasmus MC Cancer Institute, University Medical Center
Syrigos, Konstantinos Sotiria General Hospital
Livi, Lorenzo Department of Biomedical, Experimental and Clinical Sciences “Mario Serio”, University of Florence
Paulus, Astrid Centre Hospitalier Universitaire de Liège
Kim, Sang-We Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine
Chen, Yuanbin The Cancer & Hematology Centers of Western Michigan
Felip, Enriqueta Medical Oncology Department, Vall d’Hebron University Hospital
Griesinger, Frank Pius-Hospital Oldenburg
Ohashi, Kadoaki Okayama University Hospital ORCID Kaken ID researchmap
Zalcman, Gerard Hospital Bichat-Claude Bernard
Hughes, Brett G.M. The Prince Charles Hospital, University of Queensland
Sørensen, Jens Benn Rigshospitalet
Blais, Normand Department of Medicine, Centre Hospitalier de l’Université de Montréal
Ferreira, Carlos G.M. Oncoclinicas
Lindsay, Colin R. Division of Cancer Sciences, University of Manchester and The Christie NHS Foundation Trust
Dziadziuszko, Rafal University Clinical Centre, Medical University of Gdansk
Ward, Patrick J. SCRI at OHC
Obiozor, Cynthia Chinedu Amgen Inc.
Wang, Yang Amgen Inc.
Peters, Solange Lausanne University Hospital
抄録
Objectives: To assess the efficacy and safety of sotorasib in patients with brain metastases using data from the phase 3 CodeBreaK 200 study, which evaluated sotorasib in adults with pretreated advanced or metastatic KRAS G12C-mutated non-small cell lung cancer (NSCLC).
Materials and methods: Patients with KRAS G12C-mutated NSCLC who progressed after platinum-based chemotherapy and checkpoint inhibitor therapy were randomized 1:1 to sotorasib or docetaxel. An exploratory post-hoc analysis evaluated central nervous system (CNS) progression-free survival (PFS) and time to CNS progression in patients with treated and stable brain metastases at baseline. Measures were assessed by blinded independent central review per study-modified Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM) criteria.
Results: Of the patients randomly assigned to receive sotorasib (n=171) or docetaxel (n=174), baseline CNS metastases were present in 40 (23%) and 29 (17%) patients, respectively. With a median follow-up of 20.0 months for this patient subgroup, median CNS PFS was longer with sotorasib compared with docetaxel (9.6 vs 4.5 months; hazard ratio, 0.43 [95% CI, 0.20–0.92]; P=0.02). Among patients with baseline treated CNS lesions of ≥10 mm, the percentage of patients who achieved CNS tumor shrinkage of ≥30% was two-fold higher with sotorasib than docetaxel (33.3% vs 15.4%). Treatment-related adverse events among patients with CNS lesions at baseline were consistent with those of the overall study population.
Conclusions: These results suggest intracranial activity with sotorasib complements the overall PFS benefit observed with sotorasib vs docetaxel, with safety outcomes similar to those in the general CodeBreaK 200 population.
Clinical trials registration number: NCT04303780.
キーワード
Brain metastases
KRAS G12C-mutated
Non-small cell lung cancer
NSCLC
Randomized controlled trial
Sotorasib
Survival
発行日
2025-09
出版物タイトル
Lung Cancer
207巻
出版者
Elsevier BV
開始ページ
108683
ISSN
0169-5002
NCID
AA10785743
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
© 2025 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
関連URL
isVersionOf https://doi.org/10.1016/j.lungcan.2025.108683
ライセンス
http://creativecommons.org/licenses/by/4.0/
助成情報
( Amgen )