Utilize este identificador para referenciar este registo: https://hdl.handle.net/10216/144336
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Campo DCValorIdioma
dc.creatorMaria Gabriela O. Fernandes
dc.creatorCatarina Sousa
dc.creatorMaria Jacob
dc.creatorLeonor Almeida
dc.creatorVanessa Santos
dc.creatorDavid Araújo
dc.creatorHélder Novais Bastos
dc.creatorAdriana Magalhães
dc.creatorLuís Cirnes
dc.creatorConceição Souto Moura
dc.creatorHenrique Queiroga
dc.creatorNatália Cruz-Martins
dc.creatorVenceslau Hespanhol
dc.date.accessioned2022-10-18T23:08:49Z-
dc.date.available2022-10-18T23:08:49Z-
dc.date.issued2021
dc.identifier.issn2234-943X
dc.identifier.othersigarra:491615
dc.identifier.urihttps://hdl.handle.net/10216/144336-
dc.description.abstractBackground: 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.
dc.language.isoeng
dc.rightsopenAccess
dc.titleResistance profile of osimertinib in pre-treated patients with EGFR T790M-mutated non-small cell lung cancer
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoFaculdade de Medicina Dentária
dc.contributor.uportoFaculdade de Medicina
dc.identifier.doi10.3389/fonc.2021.602924
dc.identifier.authenticusP-00T-Z8Z
Aparece nas coleções:FMDUP - Artigo em Revista Científica Internacional
FMUP - Artigo em Revista Científica Internacional
I3S - Artigo em Revista Científica Internacional

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