The real-life efficacy and safety of osimertinib in pretreated advanced non-small cell lung cancer patients with T790M mutation: A Turkish Oncology Group Study

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2022Author
Hızal, MutluBilgin, Burak
Paksoy, Nail
Açıkgöz, Özgür
Sezer, Ahmet
Gürbüz, Mustafa
Ak, Naziye
Yücel, Şebnem
Ayhan, Murat
Erol, Cihan
Demirkıran, Aykut
Mandel, Nil Molinas
Shbair, Abdallah
Gökmen, İvo
Başoğlu, Tuğba
Paydaş, Semra
Demiray, Atike Gökçen
İriağaç, Yakup
Şakalar, Teoman
Zeynelgil, Esra
Tatlı, Ali Murat
Bahçeci, Aykut
Güven, Deniz Can
Caner, Burcu
Can, Alper
Gülmez, Ahmet
Karakaş, Yusuf
Yalçın, Bülent
Demirkazık, Ahmet
Bilici, Ahmet
Aydıner, Adnan
Yumuk, Perran Fulden
Şendur, Mehmet Ali Nahit
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Hızal, M., Bilgin, B., Paksoy, N., Açıkgöz, Ö., Sezer, A., Gürbüz, M. ... Şendur, M. A. N. (2022). The real-life efficacy and safety of osimertinib in pretreated advanced non-small cell lung cancer patients with T790M mutation: A Turkish Oncology Group Study. Journal of Cancer Research and Clinical Oncology, 148(6), 1501-1508. https://dx.doi.org/10.1007/s00432-021-03748-7Abstract
Introduction Osimertinib, an irreversible third-generation EGFR-TKI, is the standard of care for second-line treatment of T790M-mutant advanced NSCLC patients whose disease progressed after first-line EGFR-TKI therapy. In this multicenter study, we aimed to determine the real-life efficacy and safety of Osimertinib in pretreated advanced NSCLC patients with T790M mutation. Materials and methods This retrospective trial included advanced T790M-mutant pretreated NSCLC patients who received Osimertinib from 24 different centers in Turkey. Primary endpoint was time-to-treatment discontinuation (TTD). Secondary endpoints were objective response rate (ORR), overall survival (OS), and safety. Results Of 163 patients, 68.7% had EGFR exon 19 deletion and 22.7% had exon 21 L858R mutation. Osimertinib was given as second-line treatment in 96 patients (58.9%) and third-line in 48 patients (29.4%). After median of 13-month follow-up, median TTD was 21.6 months with an 82.2% ORR. Estimated median OS was 32.1 months. Grade 3-4 adverse events were seen in 11.7% of the patients. Conclusion Osimertinib is a highly effective option in second- or third-line treatment of NSCLC patients with T790M mutation, with a favorable safety profile.
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Journal of Cancer Research and Clinical OncologyVolume
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