Utilize este identificador para referenciar este registo:
https://hdl.handle.net/10216/144336Registo completo
| Campo DC | Valor | Idioma |
|---|---|---|
| dc.creator | Maria Gabriela O. Fernandes | |
| dc.creator | Catarina Sousa | |
| dc.creator | Maria Jacob | |
| dc.creator | Leonor Almeida | |
| dc.creator | Vanessa Santos | |
| dc.creator | David Araújo | |
| dc.creator | Hélder Novais Bastos | |
| dc.creator | Adriana Magalhães | |
| dc.creator | Luís Cirnes | |
| dc.creator | Conceição Souto Moura | |
| dc.creator | Henrique Queiroga | |
| dc.creator | Natália Cruz-Martins | |
| dc.creator | Venceslau Hespanhol | |
| dc.date.accessioned | 2022-10-18T23:08:49Z | - |
| dc.date.available | 2022-10-18T23:08:49Z | - |
| dc.date.issued | 2021 | |
| dc.identifier.issn | 2234-943X | |
| dc.identifier.other | sigarra:491615 | |
| dc.identifier.uri | https://hdl.handle.net/10216/144336 | - |
| dc.description.abstract | 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. | |
| dc.language.iso | eng | |
| dc.rights | openAccess | |
| dc.title | Resistance profile of osimertinib in pre-treated patients with EGFR T790M-mutated non-small cell lung cancer | |
| dc.type | Artigo em Revista Científica Internacional | |
| dc.contributor.uporto | Faculdade de Medicina Dentária | |
| dc.contributor.uporto | Faculdade de Medicina | |
| dc.identifier.doi | 10.3389/fonc.2021.602924 | |
| dc.identifier.authenticus | P-00T-Z8Z | |
| Aparece nas coleções: | FMDUP - Artigo em Revista Científica Internacional FMUP - Artigo em Revista Científica Internacional I3S - Artigo em Revista Científica Internacional | |
Ficheiros deste registo:
| Ficheiro | Descrição | Tamanho | Formato | |
|---|---|---|---|---|
| 491615.pdf | 396.13 kB | Adobe PDF | ![]() Ver/Abrir |
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