Zhao Liang, Zhuang Yanzhen, Fu Kaili, Chen Peiqiong, Wang Yuhuan, Zhuo Jianfang, Liao Xiyi, Chen Haojun, Lin Qin
Department of Radiation Oncology, Xiamen Cancer Hospital, The First Affiliated Hospital of Xiamen University, Teaching Hospital of Fujian Medical University, Xiamen, China.
Department of Pathology, The First Affiliated Hospital of Xiamen University, Teaching Hospital of Fujian Medical University, Xiamen, China.
Eur J Nucl Med Mol Imaging. 2020 May;47(5):1065-1074. doi: 10.1007/s00259-019-04654-4. Epub 2020 Jan 3.
To explore the relationship between [F]fluorodeoxyglucose (F-FDG uptake) and PD-L1 expression and determine the usefulness of F-FDG PET/CT for evaluating the PD-L1 status in tumour cells (TCs) and tumour-infiltrating immune cells (TIICs) in patients with nasopharyngeal carcinoma (NPC).
We retrospectively evaluated the records of 84 eligible patients who received an initial histopathological diagnosis of NPC between December 2016 and March 2019. All tissue specimens and PET/CT images were collected prior to treatment. High PD-L1 expression in TCs and TIICs was defined as ≥ 50% of stained cells.
There was a significant difference in F-FDG uptake according to the PD-L1 status in TCs and TIICs. Univariate analysis showed that PD-L1 expression in TCs was associated with tumour maximum standardized uptake value (SUVmax) (P < 0.001), primary tumour total lesion glycolysis (TLG; P < 0.001), and T stage (P = 0.044), but not with plasma Epstein-Barr virus (EBV) load (P = 0.816), whereas PD-L1 expression in TIICs was related to SUVmax (P = 0.011), TLG (P = 0.001), T stage (P = 0.028), and plasma EBV load (P = 0.003). In multivariate logistic regression, PD-L1 expression in TCs was positively associated with SUVmax (P = 0.003) and TLG (P = 0.001), and in TIICs, negatively associated with SUVmax (P = 0.038) and plasma EBV load (P = 0.025).
F-FDG uptake in NPC lesions was positively correlated with PD-L1 expression in TCs and negatively correlated with PD-L1 expression in TIICs. Thus, F-FDG PET/CT may be useful for evaluating the PD-L1 status in patients with NPC.
探讨[F]氟脱氧葡萄糖(F-FDG摄取)与程序性死亡受体配体1(PD-L1)表达之间的关系,并确定F-FDG PET/CT在评估鼻咽癌(NPC)患者肿瘤细胞(TCs)和肿瘤浸润免疫细胞(TIICs)中PD-L1状态的实用性。
我们回顾性评估了2016年12月至2019年3月期间接受NPC初始组织病理学诊断的84例合格患者的记录。所有组织标本和PET/CT图像均在治疗前收集。TCs和TIICs中高PD-L1表达定义为染色细胞≥50%。
根据TCs和TIICs中的PD-L1状态,F-FDG摄取存在显著差异。单因素分析显示,TCs中的PD-L1表达与肿瘤最大标准化摄取值(SUVmax)(P<0.001)、原发肿瘤总病变糖酵解(TLG;P<0.001)和T分期(P=0.044)相关,但与血浆EB病毒(EBV)载量(P=0.816)无关,而TIICs中的PD-L1表达与SUVmax(P=0.011)、TLG(P=0.001)、T分期(P=0.028)和血浆EBV载量(P=0.003)相关。在多因素逻辑回归中,TCs中的PD-L1表达与SUVmax(P=0.003)和TLG(P=0.001)呈正相关,而在TIICs中,与SUVmax(P=0.038)和血浆EBV载量(P=0.025)呈负相关。
NPC病变中的F-FDG摄取与TCs中的PD-L1表达呈正相关,与TIICs中的PD-L1表达呈负相关。因此,F-FDG PET/CT可能有助于评估NPC患者的PD-L1状态。