Sakakibara Rie, Inamura Kentaro, Tambo Yuichi, Ninomiya Hironori, Kitazono Satoru, Yanagitani Noriko, Horiike Atsushi, Ohyanagi Fumiyoshi, Matsuura Yosuke, Nakao Masayuki, Mun Mingyon, Okumura Sakae, Inase Naohiko, Nishio Makoto, Motoi Noriko, Ishikawa Yuichi
Division of Pathology, The Cancer Institute, Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan; Department of Integrated Pulmonology, Tokyo Medical and Dental University, Tokyo, Japan.
Division of Pathology, The Cancer Institute, Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Clin Lung Cancer. 2017 Sep;18(5):527-534.e1. doi: 10.1016/j.cllc.2016.12.002. Epub 2016 Dec 22.
Because most lung cancers are diagnosed at advanced stages, we are forced to conduct molecular testing using small biopsy samples. Endobronchial ultrasound-transbronchial needle aspiration (EBUS-TBNA) is emerging as a minimally invasive biopsy technique. Here, we examined the usefulness of EBUS-TBNA to evaluate programmed death-ligand 1 (PD-L1) expression in lung cancer.
Using 97 consecutive cases of lung cancer diagnosed by EBUS-TBNA, from which 20 transbronchial biopsy (TBB) samples were available, we evaluated the number and morphological intactness of tumor cells in EBUS-TBNA and TBB samples. Additionally, given the intratumoral heterogeneity in primary lesions and the small sample size of biopsies, we also compared the tumor PD-L1 expression between the biopsy samples and the corresponding surgical materials.
EBUS-TBNA collected a significantly larger number of tumor cells than TBB (P < .001); the median number (interquartile range) of cells was 1149 (379-3334) in EBUS-TBNA and 435 (218-1085) in TBB. The crush rate in EBUS-TBNA was significantly lower than in TBB (P < .001). These showed the excellence of EBUS-TBNA. Additionally, PD-L1 positivity of EBUS-TBNA showed a good concordance with the corresponding primary tumor (r = 0.75; P = .086; n = 6) as well as with lymph node metastasis (r = 0.93; P = .02; n = 5). Moreover, PD-L1 positivity between EBUS-TBNA and TBB (n = 16), TBB and the corresponding primary tumor (n = 41), and lymph node metastasis and the corresponding primary tumor (n = 47) showed a moderate correlation (all r > 0.48; all P < .001), strengthening the potential concordance between EBUS-TBNA and primary tumor in PD-L1 positivity.
Our study suggests EBUS-TBNA as a promising method to evaluate PD-L1 expression in lung cancer.
由于大多数肺癌在晚期才被诊断出来,我们不得不使用小活检样本进行分子检测。支气管内超声引导下经支气管针吸活检术(EBUS-TBNA)正在成为一种微创活检技术。在此,我们研究了EBUS-TBNA评估肺癌中程序性死亡配体1(PD-L1)表达的有效性。
我们连续纳入了97例经EBUS-TBNA诊断的肺癌病例,其中有20例可获得经支气管活检(TBB)样本,我们评估了EBUS-TBNA和TBB样本中肿瘤细胞的数量和形态完整性。此外,鉴于原发性病变的肿瘤内异质性以及活检样本量较小,我们还比较了活检样本与相应手术材料之间肿瘤PD-L1的表达情况。
EBUS-TBNA收集的肿瘤细胞数量明显多于TBB(P <.001);EBUS-TBNA中细胞的中位数(四分位间距)为1149(379 - 3334),TBB中为435(218 - 1085)。EBUS-TBNA的挤压率明显低于TBB(P <.001)。这些结果显示了EBUS-TBNA的优越性。此外,EBUS-TBNA的PD-L1阳性与相应的原发性肿瘤显示出良好的一致性(r = 0.75;P =.086;n = 6),与淋巴结转移也显示出良好的一致性(r = 0.93;P =.02;n = 5)。此外,EBUS-TBNA与TBB(n = 16)、TBB与相应的原发性肿瘤(n = 41)以及淋巴结转移与相应的原发性肿瘤(n = 47)之间的PD-L1阳性显示出中度相关性(所有r > 0.48;所有P <.001),加强了EBUS-TBNA与原发性肿瘤在PD-L1阳性方面的潜在一致性。
我们的研究表明EBUS-TBNA是评估肺癌中PD-L1表达的一种有前景的方法。