Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer
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...
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Frontiers Media S.A.
2021-05-01
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Series: | Frontiers in Oncology |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fonc.2021.602924/full |
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language |
English |
format |
Article |
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DOAJ |
author |
Maria Gabriela O. Fernandes Maria Gabriela O. Fernandes Maria Gabriela O. Fernandes Catarina Sousa Maria Jacob Leonor Almeida Vanessa Santos David Araújo Hélder Novais Bastos Hélder Novais Bastos Hélder Novais Bastos Adriana Magalhães Luís Cirnes Luís Cirnes Conceição Souto Moura Henrique Queiroga Henrique Queiroga Natália Cruz-Martins Natália Cruz-Martins Natália Cruz-Martins Venceslau Hespanhol Venceslau Hespanhol Venceslau Hespanhol |
spellingShingle |
Maria Gabriela O. Fernandes Maria Gabriela O. Fernandes Maria Gabriela O. Fernandes Catarina Sousa Maria Jacob Leonor Almeida Vanessa Santos David Araújo Hélder Novais Bastos Hélder Novais Bastos Hélder Novais Bastos Adriana Magalhães Luís Cirnes Luís Cirnes Conceição Souto Moura Henrique Queiroga Henrique Queiroga Natália Cruz-Martins Natália Cruz-Martins Natália Cruz-Martins Venceslau Hespanhol Venceslau Hespanhol Venceslau Hespanhol Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer Frontiers in Oncology non-small cell lung cancer EGFR T790M mutation osimertinib resistance real-world data next generation sequencing |
author_facet |
Maria Gabriela O. Fernandes Maria Gabriela O. Fernandes Maria Gabriela O. Fernandes Catarina Sousa Maria Jacob Leonor Almeida Vanessa Santos David Araújo Hélder Novais Bastos Hélder Novais Bastos Hélder Novais Bastos Adriana Magalhães Luís Cirnes Luís Cirnes Conceição Souto Moura Henrique Queiroga Henrique Queiroga Natália Cruz-Martins Natália Cruz-Martins Natália Cruz-Martins Venceslau Hespanhol Venceslau Hespanhol Venceslau Hespanhol |
author_sort |
Maria Gabriela O. Fernandes |
title |
Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer |
title_short |
Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer |
title_full |
Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer |
title_fullStr |
Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer |
title_full_unstemmed |
Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung Cancer |
title_sort |
resistance profile of osimertinib in pre-treated patients with egfr t790m-mutated non-small cell lung cancer |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2021-05-01 |
description |
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. |
topic |
non-small cell lung cancer EGFR T790M mutation osimertinib resistance real-world data next generation sequencing |
url |
https://www.frontiersin.org/articles/10.3389/fonc.2021.602924/full |
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doaj-68360ec8c5bc4884853c9fcddfe5effc2021-05-06T04:59:19ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-05-011110.3389/fonc.2021.602924602924Resistance Profile of Osimertinib in Pre-treated Patients With EGFR T790M-Mutated Non-small Cell Lung CancerMaria Gabriela O. Fernandes0Maria Gabriela O. Fernandes1Maria Gabriela O. Fernandes2Catarina Sousa3Maria Jacob4Leonor Almeida5Vanessa Santos6David Araújo7Hélder Novais Bastos8Hélder Novais Bastos9Hélder Novais Bastos10Adriana Magalhães11Luís Cirnes12Luís Cirnes13Conceição Souto Moura14Henrique Queiroga15Henrique Queiroga16Natália Cruz-Martins17Natália Cruz-Martins18Natália Cruz-Martins19Venceslau Hespanhol20Venceslau Hespanhol21Venceslau Hespanhol22Pulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalFaculty of Medicine, University of Porto, Porto, PortugalInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalFaculty of Medicine, University of Porto, Porto, PortugalInstitute for Research and Innovation in Health (i3S), University of Porto, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, PortugalEscola Superior de Saúde (ESS), Instituo Politécnico do Porto (IPP), Porto, PortugalPathology Department, Centro Hospitalar Universitário de São João, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalFaculty of Medicine, University of Porto, Porto, PortugalFaculty of Medicine, University of Porto, Porto, PortugalInstitute for Research and Innovation in Health (i3S), University of Porto, Porto, PortugalLaboratory of Neuropsychophysiology, Faculty of Psychology and Education Sciences, University of Porto, Porto, PortugalPulmonology Department, Centro Hospitalar e Universitário de São João, Porto, PortugalFaculty of Medicine, University of Porto, Porto, PortugalInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, PortugalBackground: 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.https://www.frontiersin.org/articles/10.3389/fonc.2021.602924/fullnon-small cell lung cancerEGFR T790M mutationosimertinibresistancereal-world datanext generation sequencing |