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Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study

Background: We developed a hybrid platform using a negative combined with a positive selection strategy to capture circulating tumor cells (CTCs) and detect epidermal growth factor receptor (EGFR) mutations in patients with metastatic lung adenocarcinoma. Methods: Blood samples were collected from p...

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Autores principales: Li, Shih-Hong, Wu, Min-Hsien, Wang, Hung-Ming, Hsu, Ping-Chih, Fang, Yueh-Fu, Wang, Chih-Liang, Chu, Hui-Chun, Lin, Hung-Chih, Lee, Li-Yu, Wu, Ching-Yang, Yang, Cheng-Ta, Chen, Jen-Shi, Hsieh, Jason Chia-Hsun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505961/
https://www.ncbi.nlm.nih.gov/pubmed/36142574
http://dx.doi.org/10.3390/ijms231810661
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author Li, Shih-Hong
Wu, Min-Hsien
Wang, Hung-Ming
Hsu, Ping-Chih
Fang, Yueh-Fu
Wang, Chih-Liang
Chu, Hui-Chun
Lin, Hung-Chih
Lee, Li-Yu
Wu, Ching-Yang
Yang, Cheng-Ta
Chen, Jen-Shi
Hsieh, Jason Chia-Hsun
author_facet Li, Shih-Hong
Wu, Min-Hsien
Wang, Hung-Ming
Hsu, Ping-Chih
Fang, Yueh-Fu
Wang, Chih-Liang
Chu, Hui-Chun
Lin, Hung-Chih
Lee, Li-Yu
Wu, Ching-Yang
Yang, Cheng-Ta
Chen, Jen-Shi
Hsieh, Jason Chia-Hsun
author_sort Li, Shih-Hong
collection PubMed
description Background: We developed a hybrid platform using a negative combined with a positive selection strategy to capture circulating tumor cells (CTCs) and detect epidermal growth factor receptor (EGFR) mutations in patients with metastatic lung adenocarcinoma. Methods: Blood samples were collected from patients with pathology-proven treatment-naïve stage IV lung adenocarcinoma. Genomic DNA was extracted from CTCs collected for EGFR mutational tests. The second set of CTC-EGFR mutational tests were performed after three months of anti-cancer therapy. Results: A total of 80 samples collected from 28 patients enrolled between July 2016 and August 2018. Seventeen patients had EGFR mutations, including Exon 19 deletion (n = 11), L858R (n = 5), and de-novo T790 and L858R (n = 1). Concordance between tissue and CTCs before treatment was 88.2% in EGFR- mutant patients and 90.9% in non-mutant patients. The accuracy, sensitivity, specificity, positive predictive value, and negative predictive value of EGFR mutation tests for CTCs were 89.3%, 88.2%, 90.9%, 93.8%, and 83.3%, respectively. Conclusions: CTCs captured by a hybrid platform using a negative and positive selection strategy may serve as a suitable and reliable source of lung cancer tumor DNA for detecting EGFR mutations, including T790M.
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spelling pubmed-95059612022-09-24 Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study Li, Shih-Hong Wu, Min-Hsien Wang, Hung-Ming Hsu, Ping-Chih Fang, Yueh-Fu Wang, Chih-Liang Chu, Hui-Chun Lin, Hung-Chih Lee, Li-Yu Wu, Ching-Yang Yang, Cheng-Ta Chen, Jen-Shi Hsieh, Jason Chia-Hsun Int J Mol Sci Article Background: We developed a hybrid platform using a negative combined with a positive selection strategy to capture circulating tumor cells (CTCs) and detect epidermal growth factor receptor (EGFR) mutations in patients with metastatic lung adenocarcinoma. Methods: Blood samples were collected from patients with pathology-proven treatment-naïve stage IV lung adenocarcinoma. Genomic DNA was extracted from CTCs collected for EGFR mutational tests. The second set of CTC-EGFR mutational tests were performed after three months of anti-cancer therapy. Results: A total of 80 samples collected from 28 patients enrolled between July 2016 and August 2018. Seventeen patients had EGFR mutations, including Exon 19 deletion (n = 11), L858R (n = 5), and de-novo T790 and L858R (n = 1). Concordance between tissue and CTCs before treatment was 88.2% in EGFR- mutant patients and 90.9% in non-mutant patients. The accuracy, sensitivity, specificity, positive predictive value, and negative predictive value of EGFR mutation tests for CTCs were 89.3%, 88.2%, 90.9%, 93.8%, and 83.3%, respectively. Conclusions: CTCs captured by a hybrid platform using a negative and positive selection strategy may serve as a suitable and reliable source of lung cancer tumor DNA for detecting EGFR mutations, including T790M. MDPI 2022-09-13 /pmc/articles/PMC9505961/ /pubmed/36142574 http://dx.doi.org/10.3390/ijms231810661 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Shih-Hong
Wu, Min-Hsien
Wang, Hung-Ming
Hsu, Ping-Chih
Fang, Yueh-Fu
Wang, Chih-Liang
Chu, Hui-Chun
Lin, Hung-Chih
Lee, Li-Yu
Wu, Ching-Yang
Yang, Cheng-Ta
Chen, Jen-Shi
Hsieh, Jason Chia-Hsun
Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
title Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
title_full Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
title_fullStr Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
title_full_unstemmed Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
title_short Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
title_sort circulating egfr mutations in patients with lung adenocarcinoma by circulating tumor cell isolation systems: a concordance study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505961/
https://www.ncbi.nlm.nih.gov/pubmed/36142574
http://dx.doi.org/10.3390/ijms231810661
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