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Adequacy of endobronchial ultrasound-guided transbronchial needle aspiration samples processed as histopathological samples for genetic mutation analysis in lung adenocarcinoma

机译:经肺内支气管超声引导的经支气管穿刺针抽吸样品作为组织病理学样品进行肺腺癌基因突变分析的足够性

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摘要

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.
机译:随着分子测试的到来,对非小细胞肺癌进行表型分型变得越来越重要。已发现在表皮生长因子受体(EGFR)的酪氨酸激酶结构域编码基因中带有体细胞突变的肿瘤会增加对酪氨酸激酶抑制剂的反应性。支气管内超声引导下经支气管针抽吸术(EBUS-TBNA)是用于纵隔淋巴结取样的微创技术。目前,有关EBUS-TBNA样品适用于分子谱分析的预期数据有限。这项前瞻性研究的目的是评估经证实的原发性肺腺癌中EBUS-TBNA样品用于EGFR和间变性淋巴瘤激酶(ALK)基因突变分析的适当性。我们对2010年至2014年之间连续410例因EBUS-TBNA转诊的患者进行了前瞻性分析。未使用快速的现场细胞学评估。使用21号(21G)或22G针头获得样品,并将其制备为组织病理学样品。总共确认了91个样本为肺腺癌,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性为98.3%。在79/80例病例中可以进行EGFR突变测试(98.75%)。在5/80(6.3%)样本中检测到EGFR突变。研究期间要求进行ALK基因分析,并在21/21个样本(100%)中成功进行了分析。基因型分型的总成功率为100/101(99.0%)。这项英国研究证实,EBUS-TBNA样品作为原发性肺腺癌的EGFR和ALK基因分型的组织病理学标本,具有很高的临床实用性。针规不影响基因分型功效。

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