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Comparison of epidermal growth factor receptor mutation analysis results between surgically resected primary lung cancer and metastatic lymph nodes obtained by endobronchial ultrasound‐guided transbronchial needle aspiration

机译:手术切除的原发性肺癌与经支气管内超声引导的经支气管针吸取转移性淋巴结的表皮生长因子受体突变分析结果比较

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AbstractBackground:  Lung cancers with mutations in the epidermal growth factor receptor (EGFR) gene respond well to treatment with EGFR inhibitors. Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is considered a useful modality to obtain samples from the mediastinal and hilar lymph nodes. However, the EGFR gene status of EBUS-TBNA samples may not always match that of primary tumors.Methods:  In 14 node-positive patients diagnosed by EBUS-TBNA, EGFR mutation analysis results were compared between EBUS-TBNA samples and surgically removed primary tumors. EGFR mutation was screened with peptide nucleic acid-locked nucleic acid polymerase chain reaction (PNA-LNA PCR) clamp followed by direct sequence analysis. For one controversial case, gene mutation analyses were performed for the multiple micro-fractions of a metastatic lymph node, which exhibited the heterogeneous immunohistochemical features.Results:  EBUS-TBNA diagnosed one case of exon 21 point mutations, one case of exon 19 deletion, and 12 cases of wild-type EGFR. Results were consistent with those of surgically removed primary tumors in 13 of 14 cases. One case of wild-type EGFR diagnosed by EBUS-TBNA exhibited exon 21 point mutation in the surgically removed primary tumor. The metastatic lymph node targeted by EBUS-TBNA mostly consisted of cancer cells with wild-type EGFR; however, a minor component positive for thyroid transcription factor-1 (TTF-1) and surfactant-associated protein A (PE-10) exhibited EGFR mutation.Conclusion:  The combination of EBUS-TBNA and PNA-LNA clamp is useful for EGFR mutation analysis. However, EGFR mutation status in EBUS-TBNA samples may not be consistent with that of the primary tumor when the tumor contains few EGFR mutations.
机译:摘要背景:表皮生长因子受体(EGFR)基因突变的肺癌对EGFR抑制剂的治疗反应良好。支气管内超声引导的经支气管穿刺针抽吸术(EBUS-TBNA)被认为是从纵隔和肺门淋巴结中获取样本的有用方式。然而,EBUS-TBNA样本的EGFR基因状态可能并不总是与原发性肿瘤匹配。方法:在14名经EBUS-TBNA诊断为淋巴结阳性的患者中,比较了EBUS-TBNA样本和手术切除的原发性肿瘤的EGFR突变分析结果。 。用肽核酸锁核酸聚合酶链反应(PNA-LNA PCR)钳筛选EGFR突变,然后进行直接序列分析。对于一个有争议的案例,对转移淋巴结的多个微片段进行了基因突变分析,结果显示出异质的免疫组化特征。结果:EBUS-TBNA诊断出1例外显子21点突变,1例外显子19缺失, 12例野生型EGFR。结果与14例中的13例手术切除的原发肿瘤一致。由EBUS-TBNA诊断的一例野生型EGFR在手术切除的原发肿瘤中显示外显子21点突变。 EBUS-TBNA靶向的转移性淋巴结主要由野生型EGFR癌细胞组成。但是,甲状腺转录因子-1(TTF-1)和表面活性剂相关蛋白A(PE-10)阳性的次要成分表现出EGFR突变。结论:E EBUS-TBNA和PNA-LNA钳夹组合可用于EGFR突变分析。但是,当肿瘤中几乎没有EGFR突变时,EBUS-TBNA样品中的EGFR突变状态可能与原发性肿瘤不一致。

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