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Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report

The treatment of lung cancer has made paradigm-shift advancements in the past decade with the development of therapies directed at specific genetic alterations, such as epidermal growth factor receptor (EGFR). Here, we present a rare case of lung adenocarcinoma harboring EGFR activating mutation and...

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Autores principales: Xu, Li, Wang, Qian Z, Wu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602471/
https://www.ncbi.nlm.nih.gov/pubmed/28979143
http://dx.doi.org/10.2147/OTT.S143501
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author Xu, Li
Wang, Qian Z
Wu, Lin
author_facet Xu, Li
Wang, Qian Z
Wu, Lin
author_sort Xu, Li
collection PubMed
description The treatment of lung cancer has made paradigm-shift advancements in the past decade with the development of therapies directed at specific genetic alterations, such as epidermal growth factor receptor (EGFR). Here, we present a rare case of lung adenocarcinoma harboring EGFR activating mutation and ALK overexpression. During the EGFR-tyrosine kinase inhibitors treatment, next-generation sequencing revealed phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin pathway amplifications in tumor specimen and subsequent T790M mutation via plasma circulating tumor DNA. In conclusion, this case illustrates the existence of concomitant resistance mechanisms and demonstrates that circulating tumor DNA can reflect tumor heterogeneity.
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spelling pubmed-56024712017-10-04 Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report Xu, Li Wang, Qian Z Wu, Lin Onco Targets Ther Case Report The treatment of lung cancer has made paradigm-shift advancements in the past decade with the development of therapies directed at specific genetic alterations, such as epidermal growth factor receptor (EGFR). Here, we present a rare case of lung adenocarcinoma harboring EGFR activating mutation and ALK overexpression. During the EGFR-tyrosine kinase inhibitors treatment, next-generation sequencing revealed phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin pathway amplifications in tumor specimen and subsequent T790M mutation via plasma circulating tumor DNA. In conclusion, this case illustrates the existence of concomitant resistance mechanisms and demonstrates that circulating tumor DNA can reflect tumor heterogeneity. Dove Medical Press 2017-09-12 /pmc/articles/PMC5602471/ /pubmed/28979143 http://dx.doi.org/10.2147/OTT.S143501 Text en © 2017 Xu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Xu, Li
Wang, Qian Z
Wu, Lin
Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report
title Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report
title_full Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report
title_fullStr Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report
title_full_unstemmed Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report
title_short Adenocarcinoma of the lung with EGFR gene mutation and subsequent resistance mechanisms exploration: case report
title_sort adenocarcinoma of the lung with egfr gene mutation and subsequent resistance mechanisms exploration: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602471/
https://www.ncbi.nlm.nih.gov/pubmed/28979143
http://dx.doi.org/10.2147/OTT.S143501
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