18F-FAPI-04 PET/CT与18F-FDG PET/CT对肺腺癌临床IA期诊断准确性的比较

IF 2.1 3区 医学 Q3 RESPIRATORY SYSTEM
Journal of thoracic disease Pub Date : 2025-02-28 Epub Date: 2025-02-27 DOI:10.21037/jtd-24-1658
Han-Xiang Liang, Qi-Wen Huang, Yue-Mei He, Yuan-Qi Mai, Zhe-Lin Chen, Bao-Ping Wang, Ning Fang, Jian-Feng Hu, Xie Li, Ning Zhang, En-Tao Liu, Xin-Chun Li
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引用次数: 0

摘要

背景:氟18标记成纤维细胞活化蛋白抑制剂(18F-FAPI-04)正电子发射断层扫描/计算机断层扫描(PET/CT)显示出对晚期肺癌可视化的希望。18F-FAPI-04与氟-18标记的氟脱氧葡萄糖(18F-FDG)检测早期肺腺癌(LUAD)的准确性尚不清楚。以肺结节的手术病理为金标准,比较18F-FAPI-04 PET/CT与18F-FDG PET/CT对IA期LUAD的诊断效果,以及18F-FAPI-04摄取与IA期LUAD病理特征的相关性。方法:这项前瞻性研究于2023年2月至2023年10月对同时接受18F-FAPI-04和18F-FDG PET/CT检查的IA期LUAD患者进行了分析。计算最大标准化摄取值(SUVmax)、肿瘤与背景比(TBR)、代谢肿瘤体积(MTV)、病变总糖酵解(TLG)、FAPI avid tumor volume (FTV)、病变总FAP表达(TLF)等半定量参数。使用配对学生t检验或Wilcoxon符号秩检验对这两种模式进行比较。所有切除的肿瘤标本均采用免疫组化(IHC)染色检测成纤维细胞激活蛋白(FAP)的表达。分析18F-FAPI-04摄取与IA期LUAD病理特征的相关性。结果:本研究共纳入20例诊断为IA期LUAD的患者。20例患者共发现24个肺结节,经手术及病理证实均为IA期LUAD。其中17个结节采用FAP免疫组化染色。与18F-FDG相比,18F-FAPI-04 PET/CT在整体和分层分析中均显示IA期LUAD的SUVmax和TBR有统计学意义的增加(原位腺癌+微创腺癌组与浸润性腺癌组;中度分化vs.高分化病变;IA1期vs IA2+3期;P18F-FAPI-04 (r=0.64, P=0.005)。结论:18F-FAPI-04 PET/CT对IA期LUAD的SUVmax和TBR均高于18F-FDG PET/CT。再次确认IA期LUAD的18F-FAPI-04摄取与体外FAP表达呈正相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of the diagnostic accuracy between 18F-FAPI-04 PET/CT and 18F-FDG PET/CT in the clinical stage IA of lung adenocarcinoma.

Background: Fluorine 18-labeled fibroblast activation protein inhibitor (18F-FAPI-04) positron emission tomography/computed tomography (PET/CT) has shown promise for the visualization of advanced stage lung cancer. The accuracy of 18F-FAPI-04 compared with that of fluorine-18 labeled-fluorodeoxyglucose (18F-FDG) in detecting early lung adenocarcinoma (LUAD) remains unknown. Taking the surgical pathology of pulmonary nodule as the gold standard, the diagnostic performance of stage IA LUAD were compared between 18F-FAPI-04 PET/CT and 18F-FDG PET/CT, and the correlation between 18F-FAPI-04 uptake and pathological characteristics of stage IA LUAD.

Methods: This prospective study from February 2023 to October 2023 analyzed patients with stage IA LUAD who underwent simultaneous examinations with 18F-FAPI-04 and 18F-FDG PET/CT. Semi-quantitative parameters such as maximum standardized uptake value (SUVmax), tumor-to-background ratio (TBR), metabolic tumor volume (MTV), total lesion glycolysis (TLG), FAPI avid tumor volume (FTV), and total lesion FAP expression (TLF) were calculated. The two patterns were compared using either a paired Student's t-test or a Wilcoxon signed-rank test. Immunohistochemical (IHC) staining for detecting fibroblast activating protein (FAP) expression was performed in all resected tumor specimens. Correlation analysis was performed between 18F-FAPI-04 uptake and pathological features of stage IA LUAD.

Results: A total of 20 patients diagnosed with stage IA LUAD were included in this study. A total of 24 pulmonary nodules were identified in these 20 patients, all of whom were confirmed to have stage IA LUAD through operation and pathology. Of them, 17 nodules were stained by FAP immunohistochemistry. Compared with 18F-FDG, 18F-FAPI-04 PET/CT showed a statistically significant increase in SUVmax and TBR for stage IA LUAD, both in the overall and stratified analyses (adenocarcinoma in situ + minimally invasive adenocarcinoma groups vs. invasive adenocarcinoma groups; moderately vs. well-differentiated lesions; stage IA1 vs. IA2+3; P<0.05). The SUVmax of the intense FAP expression group was significantly higher than that of the mild FAP expression group, demonstrating a statistically significant difference (P=0.005). The FAP-IHC score was positively correlated with the SUVmax of 18F-FAPI-04 (r=0.64, P=0.005).

Conclusions: 18F-FAPI-04 PET/CT demonstrates higher SUVmax and TBR than 18F-FDG PET/CT in the detection of stage IA LUAD. It was re-assured that the 18F-FAPI-04 uptake of stage IA LUAD was positively correlated with the expression of FAP in vitro.

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来源期刊
Journal of thoracic disease
Journal of thoracic disease RESPIRATORY SYSTEM-
CiteScore
4.60
自引率
4.00%
发文量
254
期刊介绍: The Journal of Thoracic Disease (JTD, J Thorac Dis, pISSN: 2072-1439; eISSN: 2077-6624) was founded in Dec 2009, and indexed in PubMed in Dec 2011 and Science Citation Index SCI in Feb 2013. It is published quarterly (Dec 2009- Dec 2011), bimonthly (Jan 2012 - Dec 2013), monthly (Jan. 2014-) and openly distributed worldwide. JTD received its impact factor of 2.365 for the year 2016. JTD publishes manuscripts that describe new findings and provide current, practical information on the diagnosis and treatment of conditions related to thoracic disease. All the submission and reviewing are conducted electronically so that rapid review is assured.
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