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镓标记的FAPI-46 PET/CT、氟代脱氧葡萄糖(FDG)PET/CT与增强CT在检测各种肿瘤方面的头对头比较。

Head-to-head comparison of  Ga-FAPI-46 PET/CT, F-FDG PET/CT, and contrast-enhanced CT for the detection of various tumors.

作者信息

Watanabe Masao, Fendler Wolfgang P, Grafe Hong, Hirmas Nader, Hamacher Rainer, Lanzafame Helena, Pabst Kim M, Hautzel Hubertus, Aigner Clemens, Kasper Stefan, von Tresckow Bastian, Stuschke Martin, Kümmel Sherko, Lugnier Celine, Hadaschik Boris, Grünwald Viktor, Zarrad Fadi, Kersting David, Siveke Jens T, Herrmann Ken, Weber Manuel

机构信息

Department of Nuclear Medicine, University Clinic Essen, Hufelandstr. 55, 45147, Essen, Germany.

Department of Nuclear Medicine, University of Duisburg-Essen and German Cancer Consortium (DKTK)-University Hospital Essen, Hufelandstr. 55, 45147, Essen, Germany.

出版信息

Ann Nucl Med. 2025 Mar;39(3):255-265. doi: 10.1007/s12149-024-01993-7. Epub 2024 Oct 23.

Abstract

OBJECTIVE

FAPI-PET/CT exhibits high tumor uptake and low background accumulation, enabling high-sensitivity tumor detection. We compared the diagnostic performance of  Ga-FAPI-46 PET/CT plus contrast-enhanced CT (CE-CT), F-FDG PET/CT plus CE-CT, and standalone CE-CT in patients with various malignancies.

METHODS

232 patients underwent  Ga-FAPI-46 PET/CT,F-FDG PET/CT, and CE-CT each within 4 weeks. Detection rates were assessed by a blinded reader, with ≥ 2 weeks between scans of the same patient to avoid recall bias. A sub-analysis of diagnostic performance was performed for 490 histopathologically validated lesions. Detection rates were compared using McNemar's test.

RESULTS

Lesion-based detection rates in  Ga-FAPI-46 PET/CT plus CE-CT, F-FDG PET/CT plus CE-CT, and CE-CT alone were 91.2% (1540/1688), 82.5% (1393/1688) and 60.2% (1016/1688). The detection rates were significantly higher for  Ga-FAPI-46 PET/CT plus CE-CT than for F-FDG PET/CT plus CE-CT (p < 0.02 for primary lesions and p < 0.001 for total, abdominopelvic nodal, liver and other visceral lesions) and CE-CT (p < 0.0001 for total, primary, cervicothoracic nodal, abdominopelvic nodal, liver, other visceral, and bone lesions). In the sub-analysis, sensitivity, specificity, positive and negative predictive value, and accuracy were 61.3%, 96.7%, 81.4%, 91.4% and 90.0% for  Ga-FAPI-46 PET/CT plus CE-CT, 57.0%, 95.7%, 75.7%, 90.5% and 88.4% for F-FDG PET/CT plus CE-CT, and 51.6%, 97.2%, 81.4%, 89.6% and 88.6% for CECT, respectively.

CONCLUSIONS

Ga-FAPI-46 PET/CT plus CE-CT demonstrates a higher tumor detection rate than F-FDG PET/CT plus CE-CT and CE-CT in a diverse spectrum of malignancies, especially for primary, abdominopelvic nodal, liver, and other visceral lesions. Further studies on which entities draw particular benefit from  Ga-FAPI-46 PET/CT are warranted to aid appropriate diagnostic workup.

TRIAL REGISTRATION

A total of N = 232 patients were analyzed. Of these, N = 50 patients were included in a prospective interventional trial (NCT05160051), and N = 175 in a prospective observational trial (NCT04571086) for correlation and clinical follow-up of PET findings; N = 7 patients were analyzed retrospectively.

摘要

目的

镓标记的成纤维细胞活化蛋白抑制剂(FAPI)-PET/CT显示出高肿瘤摄取和低背景蓄积,能够实现高灵敏度的肿瘤检测。我们比较了镓[68Ga]-FAPI-46 PET/CT联合对比增强CT(CE-CT)、氟[18F]-FDG PET/CT联合CE-CT以及单纯CE-CT在各种恶性肿瘤患者中的诊断性能。

方法

232例患者在4周内分别接受了镓[68Ga]-FAPI-46 PET/CT、氟[18F]-FDG PET/CT和CE-CT检查。由一名盲法阅片者评估检测率,同一患者的两次扫描间隔≥2周以避免回忆偏倚。对490个经组织病理学证实的病灶进行诊断性能的亚分析。使用McNemar检验比较检测率。

结果

镓[68Ga]-FAPI-46 PET/CT联合CE-CT、氟[18F]-FDG PET/CT联合CE-CT以及单纯CE-CT基于病灶的检测率分别为91.2%(1540/1688)、82.5%(1393/1688)和60.2%(1016/1688)。镓[68Ga]-FAPI-46 PET/CT联合CE-CT的检测率显著高于氟[18F]-FDG PET/CT联合CE-CT(原发性病灶p<0.02,总体、腹盆腔淋巴结、肝脏及其他内脏病灶p<0.001)和CE-CT(总体、原发性、颈胸部淋巴结、腹盆腔淋巴结、肝脏、其他内脏及骨病灶p<0.0001)。在亚分析中,镓[68Ga]-FAPI-46 PET/CT联合CE-CT的灵敏度、特异度、阳性和阴性预测值以及准确度分别为61.3%、96.7%、81.4%、91.4%和90.0%;氟[18F]-FDG PET/CT联合CE-CT分别为57.0%、95.7%、75.7%、90.5%和88.4%;CECT分别为51.6%、97.2%、81.4%、89.6%和88.6%。

结论

在多种恶性肿瘤中,镓[68Ga]-FAPI-46 PET/CT联合CE-CT显示出比氟[18F]-FDG PET/CT联合CE-CT和CE-CT更高的肿瘤检测率,尤其是对于原发性、腹盆腔淋巴结、肝脏及其他内脏病灶。有必要进一步研究哪些实体从镓[68Ga]-FAPI-46 PET/CT中特别受益,以辅助进行适当的诊断检查。

试验注册

共分析了N = 232例患者。其中,N = 50例患者纳入了一项前瞻性干预试验(NCT05160051),N = 175例患者纳入了一项前瞻性观察性试验(NCT04571086)以进行PET检查结果的相关性和临床随访;N = 7例患者进行了回顾性分析。

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