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脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值

BACKGROUND AND OBJECTIVE: The mortality rate of lung cancer meningeal metastasis is extremely high. Circulating tumor DNA (ctDNA) has been confirmed to be contain the genomic alterations present in tumors and has been used to monitor tumor progression and response to treatments. Due to the presence...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786234/
https://www.ncbi.nlm.nih.gov/pubmed/33357310
http://dx.doi.org/10.3779/j.issn.1009-3419.2020.102.42
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description BACKGROUND AND OBJECTIVE: The mortality rate of lung cancer meningeal metastasis is extremely high. Circulating tumor DNA (ctDNA) has been confirmed to be contain the genomic alterations present in tumors and has been used to monitor tumor progression and response to treatments. Due to the presence of blood-brain barrier and other factors, peripheral blood ctDNA cannot reflect the information of brain lesions for patients with meningeal metastases. However, cerebrospinal fluid ctDNA as a test sample can better reflect the genetic status of intracranial tumors and guide clinical targeted treatment of intracranial lesions. This study explored the feasibility of cerebrospinal fluid ctNDA for evaluating non-small cell lung cancer (NSCLC) meningeal metastasis and the potential clinical value of cerebrospinal fluid ctDNA detection in NSCLC meningeal metastasis. METHODS: A total of 21 patients with NSCLC meningeal metastasis were included. Tumor genomic variation was performed on the cerebrospinal fluid and peripheral blood samples of patients by second-generation gene sequencing technology. The situation was examined, and pathological evaluation of cerebrospinal fluid cytology and head magnetic resonance imaging (MRI) enhanced examination were performed. RESULTS: ctDNA was detected in the cerebrospinal fluid of 21 patients. The sensitivity of cerebrospinal fluid ctDNA detection was superior to cytology in the diagnosis of meningeal metastasis (P < 0.001). The detection rate and gene mutation abundance of cerebrospinal fluid were higher than plasma (P < 0.001). Cerebro-spinal fluid had a unique genetic profile. In 6 patients with dynamic detection, changes of ctDNA allele fraction occurred at the same time or earlier than clinical disease changes, which could timely monitor drug resistance mechanism and relapse trend. CONCLUSION: The detection rate of ctDNA in cerebrospinal fluid is higher than that in cytology and imaging. The detection of ctDNA in cerebrospinal fluid can reveal the specific mutation map of meningeal metastasis lesions. The dynamic monitoring of ctDNA in cerebrospinal fluid has hint significance for clinical response of lung cancer patients.
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spelling pubmed-77862342021-01-14 脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: The mortality rate of lung cancer meningeal metastasis is extremely high. Circulating tumor DNA (ctDNA) has been confirmed to be contain the genomic alterations present in tumors and has been used to monitor tumor progression and response to treatments. Due to the presence of blood-brain barrier and other factors, peripheral blood ctDNA cannot reflect the information of brain lesions for patients with meningeal metastases. However, cerebrospinal fluid ctDNA as a test sample can better reflect the genetic status of intracranial tumors and guide clinical targeted treatment of intracranial lesions. This study explored the feasibility of cerebrospinal fluid ctNDA for evaluating non-small cell lung cancer (NSCLC) meningeal metastasis and the potential clinical value of cerebrospinal fluid ctDNA detection in NSCLC meningeal metastasis. METHODS: A total of 21 patients with NSCLC meningeal metastasis were included. Tumor genomic variation was performed on the cerebrospinal fluid and peripheral blood samples of patients by second-generation gene sequencing technology. The situation was examined, and pathological evaluation of cerebrospinal fluid cytology and head magnetic resonance imaging (MRI) enhanced examination were performed. RESULTS: ctDNA was detected in the cerebrospinal fluid of 21 patients. The sensitivity of cerebrospinal fluid ctDNA detection was superior to cytology in the diagnosis of meningeal metastasis (P < 0.001). The detection rate and gene mutation abundance of cerebrospinal fluid were higher than plasma (P < 0.001). Cerebro-spinal fluid had a unique genetic profile. In 6 patients with dynamic detection, changes of ctDNA allele fraction occurred at the same time or earlier than clinical disease changes, which could timely monitor drug resistance mechanism and relapse trend. CONCLUSION: The detection rate of ctDNA in cerebrospinal fluid is higher than that in cytology and imaging. The detection of ctDNA in cerebrospinal fluid can reveal the specific mutation map of meningeal metastasis lesions. The dynamic monitoring of ctDNA in cerebrospinal fluid has hint significance for clinical response of lung cancer patients. 中国肺癌杂志编辑部 2020-12-20 /pmc/articles/PMC7786234/ /pubmed/33357310 http://dx.doi.org/10.3779/j.issn.1009-3419.2020.102.42 Text en 版权所有©《中国肺癌杂志》编辑部2020 This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/.
spellingShingle 临床研究
脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值
title 脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值
title_full 脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值
title_fullStr 脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值
title_full_unstemmed 脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值
title_short 脑脊液ctDNA对非小细胞肺癌脑膜转移患者的临床价值
title_sort 脑脊液ctdna对非小细胞肺癌脑膜转移患者的临床价值
topic 临床研究
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786234/
https://www.ncbi.nlm.nih.gov/pubmed/33357310
http://dx.doi.org/10.3779/j.issn.1009-3419.2020.102.42
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