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De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer

BACKGROUND: Metastatic epidermal growth factor receptor-mutated (EGFR(+)) non-small-cell lung cancer (NSCLC) can present de novo or following previous nonmetastatic disease (secondary). Potential differences between these two patient subsets are unclear at present. METHODS: We retrospectively analyz...

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Autores principales: Bozorgmehr, Farastuk, Kazdal, Daniel, Chung, Inn, Kirchner, Martina, Magios, Nikolaus, Kriegsmann, Mark, Allgäuer, Michael, Klotz, Laura V., Muley, Thomas, El Shafie, Rami A., Fischer, Jürgen R., Faehling, Martin, Stenzinger, Albrecht, Thomas, Michael, Christopoulos, Petros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063726/
https://www.ncbi.nlm.nih.gov/pubmed/33898315
http://dx.doi.org/10.3389/fonc.2021.640048
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author Bozorgmehr, Farastuk
Kazdal, Daniel
Chung, Inn
Kirchner, Martina
Magios, Nikolaus
Kriegsmann, Mark
Allgäuer, Michael
Klotz, Laura V.
Muley, Thomas
El Shafie, Rami A.
Fischer, Jürgen R.
Faehling, Martin
Stenzinger, Albrecht
Thomas, Michael
Christopoulos, Petros
author_facet Bozorgmehr, Farastuk
Kazdal, Daniel
Chung, Inn
Kirchner, Martina
Magios, Nikolaus
Kriegsmann, Mark
Allgäuer, Michael
Klotz, Laura V.
Muley, Thomas
El Shafie, Rami A.
Fischer, Jürgen R.
Faehling, Martin
Stenzinger, Albrecht
Thomas, Michael
Christopoulos, Petros
author_sort Bozorgmehr, Farastuk
collection PubMed
description BACKGROUND: Metastatic epidermal growth factor receptor-mutated (EGFR(+)) non-small-cell lung cancer (NSCLC) can present de novo or following previous nonmetastatic disease (secondary). Potential differences between these two patient subsets are unclear at present. METHODS: We retrospectively analyzed characteristics of tyrosine kinase inhibitor (TKI)-treated patients with de novo vs. secondary metastatic EGFR(+) NSCLC until December 2019 (n = 401). RESULTS: De novo metastatic disease was 4× more frequent than secondary (n = 83/401), but no significant differences were noted regarding age (median 66 vs. 70 years), sex (65% vs. 65% females), smoking history (67% vs. 62% never/light-smokers), and histology (both >95% adenocarcinoma). Patients with secondary metastatic disease showed a better ECOG performance status (PS 0–1 67%–32% vs. 46%–52%, p = 0.003), fewer metastatic sites (mean 1.3 vs. 2.0, p < 0.001), and less frequent brain involvement (16% vs. 28%, p = 0.022) at the time of stage IV diagnosis. Progression-free survival (PFS) under TKI (median 17 for secondary vs. 12 months for de novo, p = 0.26) and overall survival (OS, 29 vs. 25 months, respectively, p = 0.47) were comparable. EGFR alterations (55% vs. 60% exon 19 deletions), TP53 mutation rate at baseline (47% vs. 43%, n = 262), and T790M positivity at the time of TKI failure (51% vs. 56%, n = 193) were also similar. OS according to differing characteristics, e.g., presence or absence of brain metastases (19–20 or 30–31 months, respectively, p = 0.001), and ECOG PS 0 or 1 or 2 (32–34 or 20–23 or 5–7 months, respectively, p < 0.001), were almost identical for de novo and secondary metastatic disease. CONCLUSIONS: Despite the survival advantage reported in the pre-TKI era for relapsed NSCLC, molecular features and outcome of TKI-treated metastatic EGFR(+) tumors are currently independent of preceding nonmetastatic disease. This simplifies design of outcome studies and can assist prognostic considerations in everyday management of patients with secondary metastatic EGFR(+) tumors.
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spelling pubmed-80637262021-04-24 De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer Bozorgmehr, Farastuk Kazdal, Daniel Chung, Inn Kirchner, Martina Magios, Nikolaus Kriegsmann, Mark Allgäuer, Michael Klotz, Laura V. Muley, Thomas El Shafie, Rami A. Fischer, Jürgen R. Faehling, Martin Stenzinger, Albrecht Thomas, Michael Christopoulos, Petros Front Oncol Oncology BACKGROUND: Metastatic epidermal growth factor receptor-mutated (EGFR(+)) non-small-cell lung cancer (NSCLC) can present de novo or following previous nonmetastatic disease (secondary). Potential differences between these two patient subsets are unclear at present. METHODS: We retrospectively analyzed characteristics of tyrosine kinase inhibitor (TKI)-treated patients with de novo vs. secondary metastatic EGFR(+) NSCLC until December 2019 (n = 401). RESULTS: De novo metastatic disease was 4× more frequent than secondary (n = 83/401), but no significant differences were noted regarding age (median 66 vs. 70 years), sex (65% vs. 65% females), smoking history (67% vs. 62% never/light-smokers), and histology (both >95% adenocarcinoma). Patients with secondary metastatic disease showed a better ECOG performance status (PS 0–1 67%–32% vs. 46%–52%, p = 0.003), fewer metastatic sites (mean 1.3 vs. 2.0, p < 0.001), and less frequent brain involvement (16% vs. 28%, p = 0.022) at the time of stage IV diagnosis. Progression-free survival (PFS) under TKI (median 17 for secondary vs. 12 months for de novo, p = 0.26) and overall survival (OS, 29 vs. 25 months, respectively, p = 0.47) were comparable. EGFR alterations (55% vs. 60% exon 19 deletions), TP53 mutation rate at baseline (47% vs. 43%, n = 262), and T790M positivity at the time of TKI failure (51% vs. 56%, n = 193) were also similar. OS according to differing characteristics, e.g., presence or absence of brain metastases (19–20 or 30–31 months, respectively, p = 0.001), and ECOG PS 0 or 1 or 2 (32–34 or 20–23 or 5–7 months, respectively, p < 0.001), were almost identical for de novo and secondary metastatic disease. CONCLUSIONS: Despite the survival advantage reported in the pre-TKI era for relapsed NSCLC, molecular features and outcome of TKI-treated metastatic EGFR(+) tumors are currently independent of preceding nonmetastatic disease. This simplifies design of outcome studies and can assist prognostic considerations in everyday management of patients with secondary metastatic EGFR(+) tumors. Frontiers Media S.A. 2021-04-09 /pmc/articles/PMC8063726/ /pubmed/33898315 http://dx.doi.org/10.3389/fonc.2021.640048 Text en Copyright © 2021 Bozorgmehr, Kazdal, Chung, Kirchner, Magios, Kriegsmann, Allgäuer, Klotz, Muley, El Shafie, Fischer, Faehling, Stenzinger, Thomas and Christopoulos https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Bozorgmehr, Farastuk
Kazdal, Daniel
Chung, Inn
Kirchner, Martina
Magios, Nikolaus
Kriegsmann, Mark
Allgäuer, Michael
Klotz, Laura V.
Muley, Thomas
El Shafie, Rami A.
Fischer, Jürgen R.
Faehling, Martin
Stenzinger, Albrecht
Thomas, Michael
Christopoulos, Petros
De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer
title De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer
title_full De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer
title_fullStr De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer
title_full_unstemmed De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer
title_short De Novo Versus Secondary Metastatic EGFR-Mutated Non-Small-Cell Lung Cancer
title_sort de novo versus secondary metastatic egfr-mutated non-small-cell lung cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063726/
https://www.ncbi.nlm.nih.gov/pubmed/33898315
http://dx.doi.org/10.3389/fonc.2021.640048
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