Real-world implementation of sequential targeted therapies for EGFR-mutated lung cancer

Background: Epidermal growth factor receptor-mutated (EGFR+) non-small-cell lung cancer (NSCLC) patients failing tyrosine kinase inhibitors (TKI) can benefit from next-line targeted therapies, but implementation is challenging. Methods: EGFR+ NSCLC patients treated with first/second-generation (1G/2...

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Veröffentlicht in:Therapeutic advances in medical oncology 2021, Vol.13, p.1758835921996509-1758835921996509, Article 1758835921996509
Hauptverfasser: Magios, Nikolaus, Bozorgmehr, Farastuk, Volckmar, Anna-Lena, Kazdal, Daniel, Kirchner, Martina, Herth, Felix J., Heussel, Claus-Peter, Eichhorn, Florian, Meister, Michael, Muley, Thomas, Elshafie, Rami A., Fischer, Jürgen R., Faehling, Martin, Kriegsmann, Mark, Schirmacher, Peter, Bischoff, Helge, Stenzinger, Albrecht, Thomas, Michael, Christopoulos, Petros
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Sprache:eng
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Zusammenfassung:Background: Epidermal growth factor receptor-mutated (EGFR+) non-small-cell lung cancer (NSCLC) patients failing tyrosine kinase inhibitors (TKI) can benefit from next-line targeted therapies, but implementation is challenging. Methods: EGFR+ NSCLC patients treated with first/second-generation (1G/2G) TKI at our institution with a last follow-up after osimertinib approval (February 2016), were analyzed retrospectively, and the results compared with published data under osimertinib. Results: A total of 207 patients received erlotinib (37%), gefitinib (16%) or afatinib (47%). The median age was 66 years, with a predominance of female (70%), never/light-smokers (69%). T790M testing was performed in 174/202 progressive cases (86%), positive in 93/174 (53%), and followed by osimertinib in 87/93 (94%). Among the 135 deceased patients, 94 (70%) received subsequent systemic treatment (43% chemotherapy, 39% osimertinib), while 30% died without, either before (4%) or after progression, due to rapid clinical deterioration (22%), patient refusal of further therapy (2%), or severe competing illness (2%). Lack of subsequent treatment was significantly (4.5x, p 
ISSN:1758-8359
1758-8340
1758-8359
DOI:10.1177/1758835921996509