Epidermal Growth Factor Receptor Mutation Detection in Cerebrospinal Fluid of Lung Adenocarcinoma Patients with Leptomeningeal Metastasis
Autor: | Qiong Zhan, Xiaoyu Ji, Ruofan Huang, Xinli Zhou, Li Liao, Mengxi Ge, Xiaohua Liang |
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Rok vydání: | 2019 |
Předmět: |
Male
0301 basic medicine Cancer Research Lung Neoplasms medicine.drug_class Adenocarcinoma of Lung Tyrosine-kinase inhibitor 03 medical and health sciences 0302 clinical medicine Cerebrospinal fluid medicine Humans Radiology Nuclear Medicine and imaging Mutation detection Epidermal growth factor receptor Neoplasm Metastasis Cerebrospinal Fluid Retrospective Studies Pharmacology Lung integumentary system biology business.industry General Medicine Middle Aged medicine.disease ErbB Receptors Treatment Outcome 030104 developmental biology medicine.anatomical_structure Oncology 030220 oncology & carcinogenesis Mutation Cancer research biology.protein Adenocarcinoma Female Non small cell business Meningeal Carcinomatosis Leptomeningeal metastasis |
Zdroj: | Cancer Biotherapy and Radiopharmaceuticals. 34:128-133 |
ISSN: | 1557-8852 1084-9785 |
Popis: | Epidermal growth factor receptor (EGFR) mutations are associated with leptomeningeal metastases (LM) of nonsmall cell lung cancer and sensitivity to tyrosine kinase inhibitor (TKI) treatment. Owing to the difficulty of obtaining carcinomatous meningeal tissue for analysis, cerebrospinal fluid (CSF) might be an alternative.To investigate the EGFR mutation detection in the CSF of lung adenocarcinoma patients with LM.Twenty-five lung adenocarcinoma patients with LM diagnosed by CSF cytology were retrospectively evaluated. The results of EGFR mutation detection in CSF, the treatment plan, and clinical outcome information were recorded.Nineteen patients had a known EGFR status in their primary tumors. Twenty patients received EGFR mutation analysis in CSF after LM diagnosis and 14 of them with a known EGFR mutation status of both primary tumors and CSF. Ten (71.4%) had the same EGFR gene status. In primary tumors, no T790M mutations were detected, whereas in CSF, 2 L858R cases and 1 19del case had T790M mutations at the same time. The detection rate of T790M mutations in CSF was 18.1% (2 of 11) in all cases with EGFR-sensitive mutations in the primary lesion.EGFR mutation detection in CSF of lung adenocarcinoma patients with LM might be an alternative when leptomeningeal biopsy cannot be applied and may help to guide TKI treatments. |
Databáze: | OpenAIRE |
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