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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Main Authors: Maria Gabriela O. Fernandes, Catarina Sousa, Maria Jacob, Leonor Almeida, Vanessa Santos, David Araújo, Hélder Novais Bastos, Adriana Magalhães, Luís Cirnes, Conceição Souto Moura, Henrique Queiroga, Natália Cruz-Martins, Venceslau Hespanhol
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.602924/full
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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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spelling 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