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Ga 标记成纤维细胞激活蛋白抑制剂 (Ga-FAPI) PET 用于胰腺导管腺癌:Ga-FAPI PET 观察性试验的数据。

Ga-Labeled Fibroblast Activation Protein Inhibitor (Ga-FAPI) PET for Pancreatic Adenocarcinoma: Data from the Ga-FAPI PET Observational Trial.

机构信息

Department of Nuclear Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Department of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, Essen, Germany.

出版信息

J Nucl Med. 2023 Dec 1;64(12):1910-1917. doi: 10.2967/jnumed.122.264827.

Abstract

The fibroblast activation protein (FAP) is highly expressed on carcinoma-associated fibroblasts in the stroma of pancreatic cancer and thus is a promising target for imaging and therapy. Preliminary data on PET imaging with radiolabeled FAP inhibitors (FAPIs) demonstrate superior tumor detection. Here we assess the accuracy of FAP-directed PET in patients with pancreatic cancer. Of 64 patients with suspected or proven pancreatic cancer, 62 (97%) were included in the data analysis of the Ga-FAPI PET observational trial (NCT04571086). All of these patients underwent contrast-enhanced CT, and 38 patients additionally underwent F-FDG PET. The primary study endpoint was the association of Ga-FAPI PET uptake intensity and histopathologic FAP expression. Secondary endpoints were detection rate, diagnostic performance, interreader reproducibility, and change in management. Datasets were interpreted by 2 masked readers. The primary endpoint was met: The association between Ga-FAPI SUV and histopathologic FAP expression was significant (Spearman , 0.48; = 0.04). For histopathology-validated lesions, Ga-FAPI PET showed high sensitivity and positive predictive values (PPVs) on per-patient (sensitivity, 100%; PPV, 96.3%) and per-region (sensitivity, 100%; PPV, 97.0%) bases. In a head-to-head comparison versus F-FDG or contrast-enhanced CT, Ga-FAPI detected more tumor on a per-lesion (84.7% vs. 46.5% vs. 52.9%), per-patient (97.4% vs. 73.7% vs. 92.1%), or per-region (32.6% vs. 18.8% vs. 23.7%) basis, respectively. Ga-FAPI PET readers showed substantial overall agreement on the basis of the Fleiss κ: primary κ, 0.77 (range, 0.66-0.88). Minor and major changes in clinical management occurred in 5 patients (8.4%) after Ga-FAPI PET. We confirmed an association of Ga-FAPI PET SUV and histopathologic FAP expression in pancreatic cancer patients. Additionally, we found high detection rate and diagnostic accuracy, superior to those of F-FDG PET/CT. Ga-FAPI might become a powerful diagnostic tool for pancreatic cancer work-up.

摘要

成纤维细胞激活蛋白(FAP)在胰腺癌基质中的癌相关成纤维细胞中高度表达,因此是成像和治疗的有前途的靶点。用放射性标记的 FAP 抑制剂(FAPIs)进行 PET 成像的初步数据表明肿瘤检测具有优越性。在这里,我们评估了 FAP 导向的 PET 在胰腺癌患者中的准确性。在 64 例疑似或确诊为胰腺癌的患者中,有 62 例(97%)纳入了 Ga-FAPI PET 观察性试验的数据分析(NCT04571086)。所有这些患者均接受了对比增强 CT 检查,其中 38 例患者还接受了 F-FDG PET 检查。主要研究终点是 Ga-FAPI PET 摄取强度与组织病理学 FAP 表达的相关性。次要终点是检测率、诊断性能、两位读者的可重复性以及治疗方式的改变。数据集由 2 位盲法读者进行解读。主要终点达到了:Ga-FAPI SUV 与组织病理学 FAP 表达之间存在显著相关性(Spearman ,0.48; = 0.04)。对于经组织病理学验证的病变,Ga-FAPI PET 在每例患者(敏感性 100%,阳性预测值 96.3%)和每区域(敏感性 100%,阳性预测值 97.0%)的基础上均显示出较高的敏感性和阳性预测值。在与 F-FDG 或对比增强 CT 的头对头比较中,Ga-FAPI 在每病灶(84.7%比 46.5%比 52.9%)、每患者(97.4%比 73.7%比 92.1%)或每区域(32.6%比 18.8%比 23.7%)的基础上检测到更多的肿瘤。基于 Fleiss κ,Ga-FAPI PET 读者在总体上具有实质性的一致性:主要 κ 值为 0.77(范围,0.66-0.88)。5 例患者(8.4%)在 Ga-FAPI PET 后出现了临床管理的轻微和重大改变。我们证实了 Ga-FAPI PET SUV 与胰腺癌患者组织病理学 FAP 表达之间的相关性。此外,我们发现其检测率和诊断准确性均高于 F-FDG PET/CT。Ga-FAPI 可能成为胰腺癌检查的有力诊断工具。

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