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Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples

BACKGROUND: Evaluating the molecular characteristics of brain metastases is limited by difficult access and by the blood–brain barrier, which prevents circulating tumor DNA (ctDNA) from entering the blood. In this study, we aimed to compare the sequencing results from cerebrospinal fluid (CSF) ctDNA...

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Autores principales: Ma, Chunhua, Yang, Xueling, Xing, Wenge, Yu, Haipeng, Si, Tongguo, Guo, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049513/
https://www.ncbi.nlm.nih.gov/pubmed/31944608
http://dx.doi.org/10.1111/1759-7714.13300
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author Ma, Chunhua
Yang, Xueling
Xing, Wenge
Yu, Haipeng
Si, Tongguo
Guo, Zhi
author_facet Ma, Chunhua
Yang, Xueling
Xing, Wenge
Yu, Haipeng
Si, Tongguo
Guo, Zhi
author_sort Ma, Chunhua
collection PubMed
description BACKGROUND: Evaluating the molecular characteristics of brain metastases is limited by difficult access and by the blood–brain barrier, which prevents circulating tumor DNA (ctDNA) from entering the blood. In this study, we aimed to compare the sequencing results from cerebrospinal fluid (CSF) ctDNA versus plasma ctDNA, plasma circulating tumor cells (CTCs), and brain tissue specimens from patients with brain metastasis from non‐small cell lung cancer (NSCLC). METHODS: This was a prospective study of 21 consecutive patients with NSCLC and brain metastasis diagnosed between April 2018 and January 2019. Samples of CSF and peripheral blood were obtained from all 21 patients. Brain tissues were obtained from five patients after surgical resection. Next‐generation sequencing was performed using the Ion system. Single nucleotide variants (SNVs) and small insertions or deletions (indels) were searched. RESULTS: Mutations were detected in the CSF ctDNA of 20 (95.2%) patients. The detection rate of epidermal growth factor receptor (EGFR) mutations in CSF ctDNA was 57.1% (12/21) whereas this rate was only 23.8% (5/21) in peripheral blood ctDNA and in CTCs. EGFR mutations were found in the CSF of 9 of 11 (81.8%) patients with leptomeningeal metastases, as compared with three of 10 (30%) patients with brain parenchymal metastases. Mutations were also detected in KIT, PIK3CA, TP53, SMAD4, ATM, SMARCB1, PTEN, FLT3, GNAS, STK11, MET, CTNNB1, APC, FBXW7, ERBB4, and KDR (all >10%). The status of EGFR and TP53 mutations was consistent between CSF ctDNA and brain lesion tissue in all five patients. CONCLUSION: Sequencing of CSF ctDNA revealed specific mutation patterns in driver genes among patients with NSCLC and brain metastasis. KEY POINTS: In some small‐sample studies, the importance of cerebrospinal fluid in guiding the treatment of cancerous brain lesions has been verified in that it may reflect genomic mutations of brain tumors relatively accurately. Cerebrospinal fluid is a new form of liquid biopsy that can be helpful in improving the management of patients with brain metastasis from non‐small cell lung cancer by detecting genetic abnormalities specific to brain metastases.
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spelling pubmed-70495132020-03-05 Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples Ma, Chunhua Yang, Xueling Xing, Wenge Yu, Haipeng Si, Tongguo Guo, Zhi Thorac Cancer Original Articles BACKGROUND: Evaluating the molecular characteristics of brain metastases is limited by difficult access and by the blood–brain barrier, which prevents circulating tumor DNA (ctDNA) from entering the blood. In this study, we aimed to compare the sequencing results from cerebrospinal fluid (CSF) ctDNA versus plasma ctDNA, plasma circulating tumor cells (CTCs), and brain tissue specimens from patients with brain metastasis from non‐small cell lung cancer (NSCLC). METHODS: This was a prospective study of 21 consecutive patients with NSCLC and brain metastasis diagnosed between April 2018 and January 2019. Samples of CSF and peripheral blood were obtained from all 21 patients. Brain tissues were obtained from five patients after surgical resection. Next‐generation sequencing was performed using the Ion system. Single nucleotide variants (SNVs) and small insertions or deletions (indels) were searched. RESULTS: Mutations were detected in the CSF ctDNA of 20 (95.2%) patients. The detection rate of epidermal growth factor receptor (EGFR) mutations in CSF ctDNA was 57.1% (12/21) whereas this rate was only 23.8% (5/21) in peripheral blood ctDNA and in CTCs. EGFR mutations were found in the CSF of 9 of 11 (81.8%) patients with leptomeningeal metastases, as compared with three of 10 (30%) patients with brain parenchymal metastases. Mutations were also detected in KIT, PIK3CA, TP53, SMAD4, ATM, SMARCB1, PTEN, FLT3, GNAS, STK11, MET, CTNNB1, APC, FBXW7, ERBB4, and KDR (all >10%). The status of EGFR and TP53 mutations was consistent between CSF ctDNA and brain lesion tissue in all five patients. CONCLUSION: Sequencing of CSF ctDNA revealed specific mutation patterns in driver genes among patients with NSCLC and brain metastasis. KEY POINTS: In some small‐sample studies, the importance of cerebrospinal fluid in guiding the treatment of cancerous brain lesions has been verified in that it may reflect genomic mutations of brain tumors relatively accurately. Cerebrospinal fluid is a new form of liquid biopsy that can be helpful in improving the management of patients with brain metastasis from non‐small cell lung cancer by detecting genetic abnormalities specific to brain metastases. John Wiley & Sons Australia, Ltd 2020-01-13 2020-03 /pmc/articles/PMC7049513/ /pubmed/31944608 http://dx.doi.org/10.1111/1759-7714.13300 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ma, Chunhua
Yang, Xueling
Xing, Wenge
Yu, Haipeng
Si, Tongguo
Guo, Zhi
Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
title Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
title_full Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
title_fullStr Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
title_full_unstemmed Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
title_short Detection of circulating tumor DNA from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
title_sort detection of circulating tumor dna from non‐small cell lung cancer brain metastasis in cerebrospinal fluid samples
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049513/
https://www.ncbi.nlm.nih.gov/pubmed/31944608
http://dx.doi.org/10.1111/1759-7714.13300
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