Publication: 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
dc.contributor.author | YUMUK, PERRAN FULDEN | |
dc.contributor.authors | Hizal, Mutlu; Bilgin, Burak; Paksoy, Nail; Acikgoz, Ozgur; Sezer, Ahmet; Gurbuz, Mustafa; Ak, Naziye; Yucel, Sebnem; Ayhan, Murat; Erol, Cihan; Demirkiran, Aykut; Mandel, Nil Molinas; Shbair, Abdallah; Gokmen, Ivo; Basoglu, Tugba; Paydas, Semra; Demiray, Atike Gokcen; Iriagac, Yakup; Sakalar, Teoman; Zeynelgil, Esra; Tatli, Ali Murat; Bahceci, Aykut; Guven, Deniz Can; Caner, Burcu; Can, Alper; Gulmez, Ahmet; Karakas, Yusuf; Yalcin, Bulent; Demirkazik, Ahmet; Bilici, Ahmet; Aydiner, Adnan; Yumuk, Perran Fulden; Sendur, Mehmet Ali Nahit | |
dc.date.accessioned | 2022-03-12T22:59:22Z | |
dc.date.available | 2022-03-12T22:59:22Z | |
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.identifier.doi | 10.1007/s00432-021-03748-7 | |
dc.identifier.eissn | 1432-1335 | |
dc.identifier.issn | 0171-5216 | |
dc.identifier.pubmed | 34331582 | |
dc.identifier.uri | https://hdl.handle.net/11424/237304 | |
dc.identifier.wos | WOS:000679766900001 | |
dc.language.iso | eng | |
dc.publisher | SPRINGER | |
dc.relation.ispartof | JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Osimertinib | |
dc.subject | Non-small cell lung cancer | |
dc.subject | EGFR | |
dc.subject | T790M | |
dc.subject | Second line | |
dc.subject | CHEMOTHERAPY | |
dc.subject | THERAPY | |
dc.subject | PROGRAM | |
dc.subject | TIME | |
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 | |
dc.type | article | |
dspace.entity.type | Publication | |
local.avesis.id | ffd69354-68f8-4566-8d23-aeea4c28d53f | |
local.import.package | SS17 | |
local.indexed.at | WOS | |
local.indexed.at | SCOPUS | |
local.indexed.at | PUBMED | |
local.journal.numberofpages | 8 | |
oaire.citation.title | JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY | |
relation.isAuthorOfPublication | 4e7b3d69-6d73-4c60-89e4-d6fddfddd2aa | |
relation.isAuthorOfPublication.latestForDiscovery | 4e7b3d69-6d73-4c60-89e4-d6fddfddd2aa |