Department of Pulmonary/Critical Care, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Lung. 2024 Jun;202(3):317-324. doi: 10.1007/s00408-024-00690-6. Epub 2024 Apr 30.
The use of endobronchial ultrasound (EBUS) is standard practice for lung cancer diagnosis and staging. Next generation sequencing (NGS) for detection of genetic alterations is recommended in advanced, non-squamous, non-small-cell lung cancer (NSCLC). Existing protocols for NGS testing are minimal and reported yields vary. This study aimed to determine the yield of EBUS samples obtained for NGS using a sampling protocol at our institution and assess predictive factors to form collection protocols.
We reviewed EBUS bronchoscopies from 2016 to 2021 with non-squamous NSCLC diagnoses. For target lesions suspected to be malignant, the sampling protocol was: (a) two slides for on-site evaluation, (b) three to five fine needle aspirations rinsed into saline for immunohistochemical staining and in-house molecular markers, and (c) additional three to five rinses for NGS. Sufficiency for NGS processing was determined by the pathology department.
Two hundred and seventy-eight non-squamous NSCLC samples were obtained by EBUS (205 adenocarcinoma; 73 not otherwise specified). EBUS was performed under general anesthesia in 75.5% of cases. The overall sample adequacy for NGS testing was 57.5%. Higher adequacy rates were observed when protocol was adhered to 66.0% versus 37.2% (p < 0.001). There was no statistically significant difference based on the size of the lesion or location of the sample.
When a protocol of three to five dedicated needle rinses for NGS was followed, we nearly doubled our sample adequacy rate for NSG as compared to standard care. Studies are needed to determine the ideal collection and processing modality to preserve tissue samples for genetic sequencing.
支气管内超声(EBUS)的使用是肺癌诊断和分期的标准操作。在晚期非鳞状非小细胞肺癌(NSCLC)中,建议使用下一代测序(NGS)检测遗传改变。现有的 NGS 检测方案很少,报告的检出率也各不相同。本研究旨在确定我们机构采用采样方案进行 NGS 时获得的 EBUS 样本的检出率,并评估形成采集方案的预测因素。
我们回顾了 2016 年至 2021 年期间诊断为非鳞状 NSCLC 的 EBUS 支气管镜检查。对于疑似恶性的靶病灶,采样方案如下:(a)两个用于现场评估的载玻片,(b)三到五个细针抽吸物冲洗入生理盐水用于免疫组织化学染色和内部分子标志物,以及(c)用于 NGS 的另外三到五个冲洗物。病理科确定是否有足够的 NGS 处理样本。
通过 EBUS 获得了 278 个非鳞状 NSCLC 样本(205 个腺癌;73 个未特指)。75.5%的病例在全身麻醉下进行 EBUS。总体而言,用于 NGS 检测的样本充足率为 57.5%。当遵循方案时,观察到更高的充足率 66.0%与 37.2%(p<0.001)。根据病变的大小或样本的位置,没有统计学上的显著差异。
当遵循用于 NGS 的三到五个专用针冲洗的方案时,与标准护理相比,我们将 NSG 的样本充足率提高了近一倍。需要进一步研究以确定用于遗传测序的理想采集和处理方式,以保存组织样本。