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Resistance profile of osimertinib in pre-treated patients with EGFR T790M-mutated non-small cell lung cancer

Title
Resistance profile of osimertinib in pre-treated patients with EGFR T790M-mutated non-small cell lung cancer
Type
Article in International Scientific Journal
Year
2021
Authors
Maria Gabriela O. Fernandes
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FMUP
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Catarina Sousa
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Maria Jacob
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Leonor Almeida
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Vanessa Santos
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David Araújo
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Hélder Novais Bastos
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FMUP
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Adriana Magalhães
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Luís Cirnes
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Conceição Souto Moura
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Henrique Queiroga
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FMUP
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Natália Cruz-Martins
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FMDUP
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Journal
Title: Frontiers in OncologyImported from Authenticus Search for Journal Publications
Vol. 11 No. Article 602924
ISSN: 2234-943X
Publisher: Frontiers Media
Other information
Authenticus ID: P-00T-Z8Z
Abstract (EN): Background: Osimertinib efficacy in pre-treated patients with epidermal growth factor receptor (EGFR) T790M-mutated non-small cell lung cancer (NSCLC) has been demonstrated in clinical trials, but real-world data, particularly regarding resistance profile, remains limited. This study aims to analyze the resistance mechanisms acquired after treatment with Osimertinib. Methods: Clinical outcomes and molecular results from re-biopsies at the time of osimertinib progression of EGFR T790M-mutated NSCLC patient were analyzed. Results: Twenty-one patients with stage IV adenocarcinoma were included [median 69 years; 57.1% female; 85.7% never-smokers; 23.8% ECOG performance status (PS) >= 2]. Median PFS and OS were 13.4 (95% CI: 8.0-18.9) and 26.4 (95% IC: 8.9-43.8) months, respectively. At the time of analysis, 10 patients had tumor progression (47.6%). T790M loss occurred in 50%, being associated with earlier progression (median PFS 8.1 vs. 21.4 months, p = 0.011). Diverse molecular alterations were identified, including C797S mutation (n = 1), PIK3CA mutation (n = 2), MET amplification (n = 1), CTNNB1 mutation (n = 1), and DCTN1-ALK fusion (n = 1). Histological transformation into small cell carcinoma occurred in one patient. Conclusions: This real-world life study highlights the relevance of re-biopsy at the time of disease progression, contributing to understand resistance mechanisms and to guide treatment strategies.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 7
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602924 396.13 KB
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