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肺癌患者PET/CT上PD-L1表达与[F]FAPI及[F]FDG摄取之间的关系

Relationship between PD-L1 expression and [F]FAPI versus [F]FDG uptake on PET/CT in lung cancer.

作者信息

Qin Jingjie, Han Chao, Li Haoqian, Wang Zhendan, Hu Xudong, Liu Lanping, Zhu Shouhui, Zhao Jingjing, Sun Yuhong, Wei Yuchun

机构信息

Department of Radiology, Shandong Cancer Hospital and Institute, Shandong First Medical University, Shandong Academy of Medical Sciences, No. 440 Jiyan Road, Jinan, Shandong, 250117, China.

Shandong University Cancer Center, Jinan, Shandong, China.

出版信息

Eur J Nucl Med Mol Imaging. 2025 Mar 21. doi: 10.1007/s00259-025-07201-6.

Abstract

PURPOSE

To investigate the correlation between [F] labeled fibroblast activation protein inhibitor (FAPI) positron emission tomography (PET)/computed tomography (CT) uptake and programmed death ligand 1 (PD-L1) expression in lung cancer and evaluate the predictive value of [F]FAPI PET/CT for PD-L1 expression compared with [F]fluorodeoxyglucose ([F]FDG) PET/CT.

METHODS

This single-center retrospective study consecutively enrolled patients with pathologically confirmed lung cancer who underwent [F]FAPI and [F]FDG PET/CT scans within 2 weeks, with a minimum interval of 20 h. PD-L1 expression was assessed using immunohistochemistry and stratified into three groups. PET/CT uptake parameters included the maximum standard uptake value (SUV) in the biopsy tumor or mediastinal metastasis lymph nodes area and the mean SUV (SUV) of normal tissue (lung and blood). The ratios of SUV to the SUV for each normal tissue were denoted as the tumor-to-background ratios (TBR and TBR). All statistical analyses were conducted using IBM SPSS Statistics. Normality was assessed, and for non-normally distributed data, the Kruskal-Wallis and Mann-Whitney U tests were applied. Associations between variables were evaluated using Spearman's rank correlation. All tests were two-sided, with a P-value < 0.05 considered statistically significant.

RESULTS

Among the 75 cases included on the final analysis, the TBR and TBR derived from [F]FAPI PET/CT were significantly positively correlated with PD-L1 expression (r = 0.32, P < 0.01; r = 0.26, P < 0.05). Additionally, cases with high PD-L1 expression showed significantly higher [F]FAPI uptake values (mean TBR=36.16; mean TBR=10.75) compared with those with low PD-L1 expression (mean TBR=25.10; mean TBR=8.04). No statistically significant correlation was observed between [F]FDG uptake values and PD-L1 expression level. Receiver operating characteristic analysis identified TBR on [F]FAPI PET/CT with a cutoff value of 7.76 (area under the curve = 0.68, P < 0.01, sensitivity = 75%, and specificity = 53.49%) as a significant predictor of the level of PD-L1 expression.

CONCLUSION

[F]FAPI uptake was positively correlated with PD-L1 expression in lung cancer. The combination of [F]FAPI PET/CT and PD-L1 expression may offer a more comprehensive approach to assessing the response of lung cancer to immunotherapy.

TRIAL REGISTRATION

This study was approved by the Clinical Research Ethics Committee of our institution (institutional review board approval no. SDZLEC2021-112-02).

摘要

目的

探讨[F]标记的成纤维细胞活化蛋白抑制剂(FAPI)正电子发射断层扫描(PET)/计算机断层扫描(CT)摄取与肺癌中程序性死亡配体1(PD-L1)表达之间的相关性,并评估[F]FAPI PET/CT相较于[F]氟脱氧葡萄糖([F]FDG)PET/CT对PD-L1表达的预测价值。

方法

本单中心回顾性研究连续纳入经病理证实的肺癌患者,这些患者在2周内接受了[F]FAPI和[F]FDG PET/CT扫描,最短间隔时间为20小时。采用免疫组织化学法评估PD-L1表达,并将其分为三组。PET/CT摄取参数包括活检肿瘤或纵隔转移淋巴结区域的最大标准摄取值(SUV)以及正常组织(肺和血液)的平均SUV(SUV)。每个正常组织的SUV与SUV的比值被记为肿瘤与背景比值(TBR和TBR)。所有统计分析均使用IBM SPSS Statistics进行。评估数据的正态性,对于非正态分布的数据,应用Kruskal-Wallis和Mann-Whitney U检验。使用Spearman等级相关性评估变量之间的关联。所有检验均为双侧检验,P值<0.05被认为具有统计学意义。

结果

在最终分析纳入的75例病例中,[F]FAPI PET/CT得出的TBR和TBR与PD-L1表达显著正相关(r = 0.32,P < 0.01;r = 0.26,P < 0.05)。此外,与低PD-L1表达的病例(平均TBR = 25.10;平均TBR = 8.04)相比,高PD-L1表达的病例显示出显著更高的[F]FAPI摄取值(平均TBR = 36.16;平均TBR = 10.75)。未观察到[F]FDG摄取值与PD-L1表达水平之间存在统计学显著相关性。受试者工作特征分析确定,[F]FAPI PET/CT上的TBR,截断值为7.76(曲线下面积 = 0.68,P < 0.01,灵敏度 = 75%,特异性 = 53.49%)是PD-L1表达水平的显著预测指标。

结论

[F]FAPI摄取与肺癌中的PD-L1表达呈正相关。[F]FAPI PET/CT与PD-L1表达相结合可能为评估肺癌对免疫治疗的反应提供更全面的方法。

试验注册

本研究已获得本机构临床研究伦理委员会的批准(机构审查委员会批准号SDZLEC2021-112-02)。

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