Department of Thoracic Surgery, Kyoto University Hospital, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Department of Diagnostic Pathology, Kyoto University Hospital, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Surg Today. 2020 Sep;50(9):1049-1055. doi: 10.1007/s00595-020-01989-6. Epub 2020 Mar 12.
We investigated the utility of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) to evaluate programmed cell death ligand-1 (PD-L1) expression in patients with advanced non-small cell lung cancer (NSCLC).
A retrospective chart review of patients who underwent EBUS-TBNA between April 2017 and April 2019 was conducted. Among patients diagnosed with NSCLC, we investigated the rate of successful evaluation of tumor PD-L1 expression, compared the relevant factors between patients with evaluable and those with unevaluable PD-L1 expression, and examined the response to immune checkpoint inhibitors (ICIs) after EBUS-TBNA.
Of the 40 patients assessed, 32 (80%) had evaluable PD-L1 expression. Patients with evaluable PD-L1 expression were older than those with unevaluable PD-L1 expression (p = 0.017), and we noted a tendency for a larger diameter of the biopsied lymph node (p = 0.12). The response rate to ICIs was 100% in patients with a tumor proportion score (TPS) ≥ 50%, 33% in those with a TPS 1-49%, and 0% in those with a TPS < 1%.
The diagnostic yield of EBUS-TBNA to evaluate PD-L1 expression in advanced NSCLC appeared acceptable in association with relevant clinical outcomes after treatment with ICIs. A further prospective study with a larger sample size is required to confirm our findings.
我们研究了支气管内超声引导下经支气管针吸活检术(EBUS-TBNA)在评估晚期非小细胞肺癌(NSCLC)患者程序性死亡配体-1(PD-L1)表达中的应用。
对 2017 年 4 月至 2019 年 4 月期间接受 EBUS-TBNA 的患者进行了回顾性病历分析。在诊断为 NSCLC 的患者中,我们调查了肿瘤 PD-L1 表达评估成功率,比较了可评估和不可评估 PD-L1 表达患者的相关因素,并检查了 EBUS-TBNA 后对免疫检查点抑制剂(ICIs)的反应。
在评估的 40 例患者中,32 例(80%)有可评估的 PD-L1 表达。可评估 PD-L1 表达的患者比不可评估 PD-L1 表达的患者年龄更大(p=0.017),并且活检淋巴结的直径更大(p=0.12)。肿瘤比例评分(TPS)≥50%的患者对 ICI 的反应率为 100%,TPS 为 1-49%的患者为 33%,TPS <1%的患者为 0%。
EBUS-TBNA 评估晚期 NSCLC 中 PD-L1 表达的诊断率与 ICIs 治疗后的相关临床结局相关,似乎可以接受。需要进一步的前瞻性研究来证实我们的发现。