dc.contributor.author | Hizal, Mutlu | |
dc.contributor.author | Bilgin, Burak | |
dc.contributor.author | Paksoy, Nail | |
dc.contributor.author | Acikgoz, Ozgur | |
dc.contributor.author | Sezer, Ahmet | |
dc.contributor.author | Gurbuz, Mustafa | |
dc.contributor.author | Ak, Naziye | |
dc.contributor.author | Yucel, Sebnem | |
dc.contributor.author | Ayhan, Murat | |
dc.contributor.author | Erol, Cihan | |
dc.contributor.author | Demirkiran, Aykut | |
dc.contributor.author | Mandel, Nil Molinas | |
dc.contributor.author | Shbair, Abdallah | |
dc.contributor.author | Gokmen, Ivo | |
dc.contributor.author | Basoglu, Tugba | |
dc.contributor.author | Paydas, Semra | |
dc.contributor.author | Demiray, Atike Gokcen | |
dc.contributor.author | Iriagac, Yakup | |
dc.contributor.author | Sakalar, Teoman | |
dc.contributor.author | Zeynelgil, Esra | |
dc.contributor.author | Tatli, Ali Murat | |
dc.contributor.author | Bahceci, Aykut | |
dc.contributor.author | Guven, Deniz Can | |
dc.contributor.author | Caner, Burcu | |
dc.contributor.author | Can, Alper | |
dc.contributor.author | Gulmez, Ahmet | |
dc.contributor.author | Karakas, Yusuf | |
dc.contributor.author | Yalcin, Bulent | |
dc.contributor.author | Demirkazik, Ahmet | |
dc.contributor.author | Bilici, Ahmet | |
dc.contributor.author | Aydiner, Adnan | |
dc.contributor.author | Yumuk, Perran Fulden | |
dc.contributor.author | Sendur, Mehmet Ali Nahit | |
dc.date.accessioned | 2022-08-26T08:07:33Z | |
dc.date.available | 2022-08-26T08:07:33Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 0171-5216 | en_US |
dc.identifier.uri | https://link.springer.com/article/10.1007/s00432-021-03748-7 | |
dc.identifier.uri | http://hdl.handle.net/11727/7457 | |
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. | en_US |
dc.language.iso | eng | en_US |
dc.relation.isversionof | 10.1007/s00432-021-03748-7 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Osimertinib | en_US |
dc.subject | Non-small cell lung cancer | en_US |
dc.subject | EGFR | en_US |
dc.subject | T790M | en_US |
dc.subject | Second line | en_US |
dc.title | 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 | en_US |
dc.type | article | en_US |
dc.relation.journal | JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY | en_US |
dc.identifier.volume | 148 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | 1501 | en_US |
dc.identifier.endpage | 1508 | en_US |
dc.identifier.wos | 000679766900001 | en_US |
dc.identifier.scopus | 2-s2.0-85111543488 | en_US |
dc.contributor.pubmedID | 34331582 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | en_US |