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The real-life efficacy and safety of osimertinib in pretreated advanced

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dc.contributor.author Hizal, M
dc.contributor.author Bilgin, B
dc.contributor.author Paksoy, N
dc.contributor.author Acikgoz, O
dc.contributor.author Sezer, A
dc.contributor.author Gurbuz, M
dc.contributor.author Ak, N
dc.contributor.author Yucel, S
dc.contributor.author Ayhan, M
dc.contributor.author Erol, C
dc.contributor.author Demirkiran, A
dc.contributor.author Mandel, NM
dc.contributor.author Shbair, A
dc.contributor.author Gokmen, I
dc.contributor.author Basoglu, T
dc.contributor.author Paydas, S
dc.contributor.author Demiray, AG
dc.contributor.author Iriagac, Y
dc.contributor.author Sakalar, T
dc.contributor.author Zeynelgil, E
dc.contributor.author Tatli, AM
dc.contributor.author Bahceci, A
dc.contributor.author Guven, DC
dc.contributor.author Caner, B
dc.contributor.author Can, A
dc.contributor.author Gulmez, A
dc.contributor.author Karakas, Y
dc.contributor.author Yalcin, B
dc.contributor.author Demirkazik, A
dc.contributor.author Bilici, A
dc.contributor.author Aydiner, A
dc.contributor.author Yumuk, PF
dc.contributor.author Sendur, MAN
dc.date.accessioned 2022-10-11T12:55:24Z
dc.date.available 2022-10-11T12:55:24Z
dc.date.issued 2022
dc.identifier.uri http://hdl.handle.net/11616/74849
dc.description.abstract 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.
dc.source JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
dc.title The real-life efficacy and safety of osimertinib in pretreated advanced
dc.title non-small cell lung cancer patients with T790M mutation: a Turkish
dc.title Oncology Group Study


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