Department of Oral and Maxillofacial Surgery, Hospital Universitario Central de Asturias, Asturias, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias, Instituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, Asturias. Spain.
Cancer Epidemiol Biomarkers Prev. 2019 Mar;28(3):546-554. doi: 10.1158/1055-9965.EPI-18-0779. Epub 2018 Nov 28.
The immune checkpoint PD-1 and its ligand PD-L1 are involved in the induction of immunological tolerance of solid tumors including oral squamous cell carcinoma (OSCC). The aim of the study was to establish the clinical and prognostic significance of PD-L1 in OSCC.
Tissue microarrays of 125 resected OSCC were stained with two different commercially available PD-L1 antibodies (clones E1L3N and 22C3), alongside PD-1 immunostaining.
PD-L1 expression in more than 10% of tumor cells was associated with poorer survival, and established as a clinically relevant cut-off point. This relevant PD-L1 expression was detected in 10% to 15% OSCC specimens depending on the anti-PD-L1 antibody, and showed an inverse correlation with tobacco and alcohol consumption. We consistently found that PD-L1 expression was associated with tumor recurrence and lower disease-specific survival. Multivariate analysis further revealed that neck node metastasis (HR 2.304; = 0.009) and tumor PD-L1 expression (HR 2.571; = 0.01) were significant independent factors for poor prognosis.
PD-L1 expression in more than 10% of tumor cells was a significant and independent factor of poor prognosis in OSCC.
PD-L1 expression in more than 10% of tumor cells was consistently established as a clinically relevant cut-off point by using two different antibodies. Remarkably, PD-L1 expression emerges as an independent poor prognosis marker in patients with OSCC.
免疫检查点 PD-1 及其配体 PD-L1 参与包括口腔鳞状细胞癌(OSCC)在内的实体瘤免疫耐受的诱导。本研究旨在确定 PD-L1 在 OSCC 中的临床和预后意义。
使用两种不同的商业上可获得的 PD-L1 抗体(克隆 E1L3N 和 22C3)对 125 例切除的 OSCC 组织微阵列进行染色,并进行 PD-1 免疫染色。
肿瘤细胞中 PD-L1 表达超过 10%与生存不良相关,并被确定为具有临床相关性的截止点。根据抗 PD-L1 抗体,该相关 PD-L1 表达在 10%至 15%的 OSCC 标本中被检测到,并且与烟草和酒精消费呈负相关。我们一致发现 PD-L1 表达与肿瘤复发和较低的疾病特异性生存率相关。多变量分析进一步表明,颈部淋巴结转移(HR 2.304; = 0.009)和肿瘤 PD-L1 表达(HR 2.571; = 0.01)是预后不良的显著独立因素。
肿瘤细胞中 PD-L1 表达超过 10%是 OSCC 预后不良的显著和独立因素。
使用两种不同的抗体,超过 10%的肿瘤细胞中 PD-L1 表达一致被确定为具有临床相关性的截止点。值得注意的是,PD-L1 表达在 OSCC 患者中成为独立的预后不良标志物。