Jeyabalan Abiramy, Bhatt Nidhi, Plummeridge Martin J, Medford Andrew R L
North Bristol Lung Centre and University of Bristol, North Bristol NHS Trust, Southmead Hospital, Bristol BS10 5NB, UK.
Department of Pathology, University Hospitals Bristol NHS Trust, Bristol Royal Infirmary, Bristol BS2 8HW, UK.
Mol Clin Oncol. 2016 Jan;4(1):119-125. doi: 10.3892/mco.2015.672. Epub 2015 Nov 9.
Phenotyping non-small-cell lung cancer is becoming increasingly important with the advent of molecular testing. Tumours harbouring somatic mutations in the gene that encodes for the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) have been found to increase responsiveness to tyrosine kinase inhibitors. Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is a minimally invasive technique for mediastinal node sampling. The available prospective data on EBUS-TBNA sample suitability for molecular profiling are currently limited. The aim of this prospective study was to evaluate the adequacy of EBUS-TBNA samples for EGFR and anaplastic lymphoma kinase (ALK) genetic mutation analysis in confirmed primary lung adenocarcinomas. We conducted a prospective analysis of 410 consecutive patients referred for EBUS-TBNA between 2010 and 2014. Rapid on-site cytological evaluation was not used. The samples were obtained using 21-gauge (21G) or 22G needles and were prepared as histopathological samples. A total of 91 samples were confirmed as lung adenocarcinomas and 80 of these samples were sent for EGFR mutation analysis. EBUS-TBNA had a diagnostic accuracy of 98.3% for malignancy. EGFR mutation testing was possible in 79/80 cases (98.75%). EGFR mutations were detected in 5/80 (6.3%) samples. ALK gene analysis, which became available during the study period, was requested and successfully performed in 21/21 samples (100%). The total combined genotyping success rate was 100/101 (99.0%). This UK study confirmed the high clinical utility of EBUS-TBNA samples processed as histopathological specimens for EGFR and ALK genotyping in primary lung adenocarcinoma. The needle gauge did not affect genotyping efficacy.
随着分子检测的出现,非小细胞肺癌的表型分析变得越来越重要。已发现,在编码表皮生长因子受体(EGFR)酪氨酸激酶结构域的基因中存在体细胞突变的肿瘤,对酪氨酸激酶抑制剂的反应性会增加。支气管内超声引导下经支气管针吸活检(EBUS-TBNA)是一种用于纵隔淋巴结采样的微创技术。目前,关于EBUS-TBNA样本用于分子分析的适用性的前瞻性数据有限。这项前瞻性研究的目的是评估EBUS-TBNA样本在确诊的原发性肺腺癌中进行EGFR和间变性淋巴瘤激酶(ALK)基因突变分析的充分性。我们对2010年至2014年间连续410例接受EBUS-TBNA检查的患者进行了前瞻性分析。未使用快速现场细胞学评估。样本使用21号(21G)或22G针获取,并制备成组织病理学样本。共有91个样本被确认为肺腺癌,其中80个样本被送去进行EGFR突变分析。EBUS-TBNA对恶性肿瘤的诊断准确率为98.3%。79/80例(98.75%)可进行EGFR突变检测。在5/80(6.3%)个样本中检测到EGFR突变。在研究期间可用的ALK基因分析被要求并在21/21个样本(100%)中成功进行。总的基因分型成功率为100/101(99.0%)。这项英国研究证实了将EBUS-TBNA样本处理为组织病理学标本用于原发性肺腺癌的EGFR和ALK基因分型具有很高的临床实用性。针的规格不影响基因分型效果。