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dc.contributor.authorHizal, Mutlu
dc.contributor.authorBilgin, Burak
dc.contributor.authorPaksoy, Nail
dc.contributor.authorAcikgoz, Ozgur
dc.contributor.authorSezer, Ahmet
dc.contributor.authorGurbuz, Mustafa
dc.contributor.authorAk, Naziye
dc.contributor.authorYucel, Sebnem
dc.contributor.authorAyhan, Murat
dc.contributor.authorErol, Cihan
dc.contributor.authorDemirkiran, Aykut
dc.contributor.authorMandel, Nil Molinas
dc.contributor.authorShbair, Abdallah
dc.contributor.authorGokmen, Ivo
dc.contributor.authorBasoglu, Tugba
dc.contributor.authorPaydas, Semra
dc.contributor.authorDemiray, Atike Gokcen
dc.contributor.authorIriagac, Yakup
dc.contributor.authorSakalar, Teoman
dc.contributor.authorZeynelgil, Esra
dc.contributor.authorTatli, Ali Murat
dc.contributor.authorBahceci, Aykut
dc.contributor.authorGuven, Deniz Can
dc.contributor.authorCaner, Burcu
dc.contributor.authorCan, Alper
dc.contributor.authorGulmez, Ahmet
dc.contributor.authorKarakas, Yusuf
dc.contributor.authorYalcin, Bulent
dc.contributor.authorDemirkazik, Ahmet
dc.contributor.authorBilici, Ahmet
dc.contributor.authorAydiner, Adnan
dc.contributor.authorYumuk, Perran Fulden
dc.contributor.authorSendur, Mehmet Ali Nahit
dc.date.accessioned2022-08-26T08:07:33Z
dc.date.available2022-08-26T08:07:33Z
dc.date.issued2021
dc.identifier.issn0171-5216en_US
dc.identifier.urihttps://link.springer.com/article/10.1007/s00432-021-03748-7
dc.identifier.urihttp://hdl.handle.net/11727/7457
dc.description.abstractIntroduction 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.isoengen_US
dc.relation.isversionof10.1007/s00432-021-03748-7en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectOsimertiniben_US
dc.subjectNon-small cell lung canceren_US
dc.subjectEGFRen_US
dc.subjectT790Men_US
dc.subjectSecond lineen_US
dc.titleThe real-life efficacy and safety of osimertinib in pretreated advanced non-small cell lung cancer patients with T790M mutation: a Turkish Oncology Group Studyen_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGYen_US
dc.identifier.volume148en_US
dc.identifier.issue6en_US
dc.identifier.startpage1501en_US
dc.identifier.endpage1508en_US
dc.identifier.wos000679766900001en_US
dc.identifier.scopus2-s2.0-85111543488en_US
dc.contributor.pubmedID34331582en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US


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