4.6 Article

Endobronchial ultrasound-guided transbronchial needle aspiration for identifying EGFR mutations

期刊

EUROPEAN RESPIRATORY JOURNAL
卷 35, 期 2, 页码 391-395

出版社

EUROPEAN RESPIRATORY SOC JOURNALS LTD
DOI: 10.1183/09031936.00028109

关键词

Adenocarcinoma; endobronchial ultrasonography; endobronchial ultrasonography needle aspiration; epidermal growth factor receptor; lung cancer

资金

  1. Centre for Biomedical Research in Respiratory Diseases (CibeRes
  2. Bunyola, Spain)
  3. Health Research Fund (Madrid, Spain) [070170]
  4. Spanish Society of Pulmonology and Thoracic Surgery (Barcelona, Spain)
  5. Catalan Pulmonology Society (Barcelona, Spain)
  6. Spanish Respiratory Endoscopy Association (Seville, Spain)
  7. Thematic Network of Cooperative Cancer Research (Salamanca, Spain) [RD06/0020/0056]

向作者/读者索取更多资源

The presence of somatic mutations of the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) gene in patients with advanced nonsmall cell lung cancer (NSCLC) correlates with a good response to tyrosine kinase inhibitors. The usefulness of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) for the detection of EGFR mutations in cells recovered from malignant mediastinal nodes in patients with NSCLC was assessed. All patients with lung adenocarcinoma or unspecified NSCLC referred for staging with EBUS-TBNA were included. Nodes with a short-axis diameter of >5 mm were sampled, and genomic DNA from metastatic tumour cells was obtained for analysis of exons 19 and 21. The impact of sampling on management was assessed. EGFR gene analysis of the EBUS-TBNA sample was feasible in 26 (72.2%) out of the 36 patients with lymph node metastasis. Somatic mutations of the EGFR gene were detected in tissue obtained through EBUS-TBNA in two (10%) out of 20 patients with metastasic lung adenocarcinoma. Malignant tissue samples obtained by EBUS-TBNA from patients with nodal metastasis of NSCLC are suitable for the detection of EGFR mutations in most cases, and this technique demonstrates mutated neoplastic cells in a tenth of patients with adenocarcinoma.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据