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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 | Authors: | Hizal M. Bilgin B. Paksoy N. Açıkgöz Ö. Sezer A. Gürbüz M. Ak N. Yücel, Şebnem Ayhan, Murat Erol, Cihan Demirkıran, Aykut Mandel, Nil Molinas Shbair, Abdallah Gökmen, İvo Başoğlu, Tuğba Demiray, Atike Gökçen İriağaç, Yakup Şakalar, Teoman Zeynelgil, Esra Tatlı, Ali Murat Bahçeci, Aykut Güven, Deniz Can Caner, Burcu Can, Alper Gülmez, Ahmet Karakaş, Yusuf Yalçın, Bülent Demirkazık, Ahmet Bilici, Ahmet Aydıner, Adnan Yumuk, Perran Fulden Şendur, Mehmet Ali Nahit Paydaş, Semra |
Keywords: | EGFR Non-small cell lung cancer Osimertinib Second line T790M afatinib circulating tumor DNA epidermal growth factor receptor erlotinib gefitinib osimertinib protein t790m protein unclassified drug acrylamide derivative aniline derivative epidermal growth factor receptor osimertinib protein kinase inhibitor adult advanced cancer adverse drug reaction Article brain metastasis cancer patient cancer survival clinical feature controlled study decreased appetite diarrhea drug efficacy drug safety exon fatigue female follow up gene mutation human major clinical study male multicenter study non small cell lung cancer overall survival pneumonia retrospective study skin toxicity time to treatment treatment response treatment withdrawal clinical trial genetics lung tumor mutation turkey (bird) Acrylamides Aniline Compounds Carcinoma, Non-Small-Cell Lung ErbB Receptors Humans Lung Neoplasms Mutation Protein Kinase Inhibitors Retrospective Studies Turkey |
Publisher: | Springer Science and Business Media Deutschland GmbH | 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. © 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. | URI: | https://doi.org/10.1007/s00432-021-03748-7 https://hdl.handle.net/11499/47357 |
ISSN: | 0171-5216 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu |
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