본문으로 건너뛰기
← 뒤로

The efficacy of targeted therapies in metastatic squamous cell carcinoma of the lung: a Turkish Oncology Group multicentre study.

Journal of chemotherapy (Florence, Italy) 2025 p. 1-13

Kılıçtaş B, Araz M, Oruç A, Çağlayan D, Emin G, Yıldırım A, Aydın Tİ, Hacıoğlu MB, Dişli AK, İnanç M, Uyar GC, Çakmak Öksüzoğlu ÖB, Uysal M, Koçanoğlu A, Akın Telli T, Akdağ G, Kınıkoğlu O, Işık D, Arcagök M, Urakçı Z, Şahin E, Akdoğan O, Danacı Y, Şakalar T, Avcı N, Serin Özel G, Doğu GG, Şahin Hafızoğlu E, Erdoğan AP, Alkan A, Erkan Özmarasalı B, Deligönül A, Büyükşimşek M, Karakurt Eryılmaz M, Artaç M

📝 환자 설명용 한 줄

This multicentre real-world study evaluated the efficacy of targeted therapies in Turkish patients with metastatic squamous cell lung carcinoma harbouring driver mutations.

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Kılıçtaş B, Araz M, et al. (2025). The efficacy of targeted therapies in metastatic squamous cell carcinoma of the lung: a Turkish Oncology Group multicentre study.. Journal of chemotherapy (Florence, Italy), 1-13. https://doi.org/10.1080/1120009X.2025.2601938
MLA Kılıçtaş B, et al.. "The efficacy of targeted therapies in metastatic squamous cell carcinoma of the lung: a Turkish Oncology Group multicentre study.." Journal of chemotherapy (Florence, Italy), 2025, pp. 1-13.
PMID 41414901

Abstract

This multicentre real-world study evaluated the efficacy of targeted therapies in Turkish patients with metastatic squamous cell lung carcinoma harbouring driver mutations. Sixty-four patients with alterations such as EGFR, ALK, and ROS1 who received targeted agents were retrospectively analysed. EGFR mutations were most common (67.2%). Among EGFR-TKI-treated patients, median progression-free survival (PFS) and overall survival (OS) were 12.4 and 14.3 months, respectively. Alectinib yielded a median PFS of 18.6 months and OS of 29.8 months in ALK-positive patients, while crizotinib produced a median PFS and OS of 7 months in ROS1-positive patients. The overall response rate was 50% and the disease control rate 84.4%. Although targeted therapies prolonged PFS compared with chemotherapy, this improvement did not translate into a significant OS advantage, likely influenced by retrospective design and treatment crossover. Findings represent real-world outcomes in a molecularly defined subgroup.