Thoracic Surgery, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, USA.
Pathology Services, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, USA.
Lung Cancer. 2018 May;119:85-90. doi: 10.1016/j.lungcan.2018.03.003. Epub 2018 Mar 7.
Next-generation sequencing (NGS) allows for the identification of a growing number of therapeutic and prognostic molecular targets. However, NGS typically requires greater quantities of DNA than traditional molecular testing does. Endobronchial ultrasound transbronchial needle aspiration (EBUS-TBNA) is a minimally invasive procedure used to sample central thoracic lesions, but it is not well established whether this technique provides sufficient material for NGS.
We performed a retrospective review of EBUS-TBNA at our institution (3/1/14-9/28/16). NGS was performed using a comprehensive hybrid-capture based assay (MSK-IMPACT) that detects >340 gene mutations. Samples found to be diagnostic for malignancy and for which MSK-IMPACT had been attempted were identified. Pathologic and clinical data were obtained from the medical record, and the results of MSK-IMPACT were examined.
In total, 784 EBUS-TBNA procedures were performed during the study period. MSK-IMPACT was requested for 115 malignant samples and was successful for 99 (86.1%), identifying an average of 12.7 mutations at a mean coverage depth of 806X. NGS was performed on paraffin-embedded cell blocks in 93 cases (93.9%) and on cell-free DNA in needle rinse fluid in 6 cases. The success rate of the assay improved significantly from the first third of cases (76.3%), to 92.3% for the final one-third of cases (p < 0.05).
EBUS-TBNA reliably provided adequate tissue for hybrid capture NGS, and is a suitable option for comprehensive NGS testing in patients with thoracic malignancies.
下一代测序(NGS)可鉴定出越来越多的治疗和预后分子靶标。然而,NGS 通常需要比传统分子检测更多的 DNA。支气管内超声引导经支气管针吸活检术(EBUS-TBNA)是一种微创程序,用于取样中心胸部病变,但尚不清楚该技术是否能提供足够的 NGS 材料。
我们对我院进行的 EBUS-TBNA 进行了回顾性分析(3/1/14-9/28/16)。NGS 使用基于综合杂交捕获的检测方法(MSK-IMPACT)进行,该方法可检测超过 340 个基因突变。确定对恶性肿瘤具有诊断价值且已尝试使用 MSK-IMPACT 的样本。从病历中获取病理和临床数据,并检查 MSK-IMPACT 的结果。
在研究期间共进行了 784 次 EBUS-TBNA 操作。为 115 个恶性样本请求了 MSK-IMPACT,其中 99 个(86.1%)成功,平均覆盖率为 806X,平均鉴定 12.7 个突变。在 93 例(93.9%)石蜡包埋细胞块和 6 例针洗脱液中进行了无细胞游离 DNA 的 NGS。该检测方法的成功率从前 1/3 病例的 76.3%显著提高到最后 1/3 病例的 92.3%(p<0.05)。
EBUS-TBNA 可靠地为杂交捕获 NGS 提供了足够的组织,是对胸部恶性肿瘤患者进行综合 NGS 检测的合适选择。