Regional distribution of genetic mutation in lung cancer in Turkey (REDIGMA)

The results of standard chemotherapy in lung cancer are not very satisfactory, so it is important to identify genetic mutations that provide targeted therapies. Recent reports have suggested influences of racial difference on the frequency of mutation in lung cancer. We aimed to determine the freque...

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Veröffentlicht in:Tüberküloz ve toraks 2019-09, Vol.67 (3), p.197-204
Hauptverfasser: Özçelik, Neslihan, Aksel, Nimet, Bülbül, Yılmaz, Erdoğan, Yurdanur, Güldaval, Filiz, Karabulut Gül, Şule, Bircan, Ahmet, Can, Atilla, Öz, Necdet, Şentürk, Ayşegül, Arınç, Sibel, Kılıç, Talat, Kurt, Emine Bahar, Günay, Ersin, Çağlayan, Benan, Çelebi Aydın, Derya, Başyiğit, İlknur, Savaş, İsmail, Tatar, Dursun, Arslan, Sulhattin, Kömürcüoğlu, Berna, Bayram, Mehmet, Gülmez, İnci, Doğan, Ömer Tamer, Özgün Niksarlıoğlu, Elif Yelda, Kaba, Erkan, Karaoğlanoğlu, Selen, Aydın Özgür, Esra, Özçelik, Ali Erdem, Özlü, Tevfik
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Sprache:eng
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Zusammenfassung:The results of standard chemotherapy in lung cancer are not very satisfactory, so it is important to identify genetic mutations that provide targeted therapies. Recent reports have suggested influences of racial difference on the frequency of mutation in lung cancer. We aimed to determine the frequency and regional distribution of genetic mutations of non-small cell lung cancer (NSCLC) in Turkey. Regional distribution of genetic mutations in lung cancer in Turkey (REDIGMA) study was carried out as a prospective, cross-sectional, observational study in a large number of centers in which lung cancer patients were followed and could perform genetic mutation analysis on patients' biopsy materials. The 703 patients (77.7% male, mean age 63.3 ± 12.5 years) who were diagnosed as NSCLC from 25 different centers were included in the study. Tumor samples from patients were reported as 87.1% adenocarcinoma, 6.4% squamous cell carcinoma and 6.5% other. Mutation tests were found to be positive in 18.9% of these patients. The mutations were 69.9% EGFR, 26.3% ALK, 1.6% ROS and 2.2% PDL. Mutations were higher in women and non-smokers (p
ISSN:0494-1373
DOI:10.5578/tt.68707