Back to Search Start Over

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.

Authors :
Hizal M
Bilgin B
Paksoy N
Açıkgöz Ö
Sezer A
Gürbüz M
Ak N
Yücel Ş
Ayhan M
Erol C
Demirkıran A
Mandel NM
Shbair A
Gökmen İ
Başoğlu T
Paydaş S
Demiray AG
İriağaç Y
Şakalar T
Zeynelgil E
Tatlı AM
Bahçeci A
Güven DC
Caner B
Can A
Gülmez A
Karakaş Y
Yalçın B
Demirkazık A
Bilici A
Aydıner A
Yumuk PF
Şendur MAN
Source :
Journal of cancer research and clinical oncology [J Cancer Res Clin Oncol] 2022 Jun; Vol. 148 (6), pp. 1501-1508. Date of Electronic Publication: 2021 Jul 31.
Publication Year :
2022

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.<br />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.<br />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.<br />Conclusion: Osimertinib is a highly effective option in second- or third-line treatment of NSCLC patients with T790M mutation, with a favorable safety profile.<br /> (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Details

Language :
English
ISSN :
1432-1335
Volume :
148
Issue :
6
Database :
MEDLINE
Journal :
Journal of cancer research and clinical oncology
Publication Type :
Academic Journal
Accession number :
34331582
Full Text :
https://doi.org/10.1007/s00432-021-03748-7