Department of Nuclear Medicine, University Hospital, LMU Munich, Marchioninistr. 15, 81377, Munich, Germany.
Department of Urology, University Hospital, LMU Munich, Munich, Germany.
Eur J Nucl Med Mol Imaging. 2022 Aug;49(10):3571-3580. doi: 10.1007/s00259-022-05761-5. Epub 2022 Mar 24.
[Ga]Ga-FAPI-46 is a novel positron emission tomography (PET) ligand that targets fibroblast activation protein (FAP) expression as FAP inhibitor (FAPI) and could already show promising results in several tumor entities. It could be demonstrated that an increased FAP expression correlates with tumor aggressivity in urothelial carcinoma (UC). Given the limited value of [F]FDG in UC, [Ga]Ga-FAPI-46 could add diagnostic information in staging and response assessment in UC. We present the first data of [Ga]Ga-FAPI-46 PET imaging in a pilot cohort of UC patients evaluating uptake characteristics in metastases and primary tumors.
Fifteen patients with UC prior to or after local treatment underwent [Ga]Ga-FAPI-46 PET/CT imaging for detection of metastatic spread. We compared the biodistribution in non-affected organs and tumor uptake of UC lesions by standard uptake value measurements (SUV and SUV). Additionally, metastatic sites on PET were compared to its morphological correlate on contrast-enhanced computed tomography (CT).
Overall, 64 tumor sites were detected on PET and/or CT. The highest uptake intensity was noted at the primary site (SUV 20.8 (range, 8.1-27.8)) followed by lymph node metastases (SUV 10.6 (range, 4.7-29.1)). In 4/15 (26.7%) patients there were [Ga]Ga-FAPI-46-positive lesions that were missed on standard routine CT imaging. On the other hand, 2/15 patients had suspicious prominent bipulmonary nodules as well as pelvic lymph nodes previously rated as suspicious for metastatic spread on CT, but without increased FAPI expression; here histopathology excluded malignancy.
[Ga]Ga-FAPI-46 PET shows distinctly elevated uptake in UC lesions. Therefore, the tracer has potential as a promising new biomarker in metastatic UC patients, as [Ga]Ga-FAPI-46 PET might improve detection of metastatic sites compared to CT alone. These findings highly emphasize larger studies investigating FAPI imaging in UC patients.
[Ga]Ga-FAPI-46 是一种新型的正电子发射断层扫描(PET)配体,靶向成纤维细胞激活蛋白(FAP)表达作为 FAP 抑制剂(FAPI),并已在多种肿瘤实体中显示出良好的效果。已经证明,FAP 表达增加与尿路上皮癌(UC)的肿瘤侵袭性相关。鉴于[F]FDG 在 UC 中的有限价值,[Ga]Ga-FAPI-46 可在 UC 的分期和反应评估中提供诊断信息。我们展示了在评估转移性和原发性肿瘤摄取特征的 UC 患者的试点队列中,首次进行[Ga]Ga-FAPI-46 PET 成像的数据。
15 名接受过或未接受过局部治疗的 UC 患者接受[Ga]Ga-FAPI-46 PET/CT 成像,以检测转移扩散。我们通过标准摄取值测量(SUV 和 SUV)比较非受累器官的生物分布和 UC 病变的摄取。此外,比较 PET 上的转移部位与其对比增强 CT(CT)的形态学相关性。
总体而言,在 PET 和/或 CT 上共检测到 64 个肿瘤部位。原发部位的摄取强度最高(SUV20.8(范围,8.1-27.8)),其次是淋巴结转移(SUV10.6(范围,4.7-29.1))。在 15 名患者中的 4 名(26.7%)中,[Ga]Ga-FAPI-46 阳性病变在标准常规 CT 成像中漏诊。另一方面,2 名患者的双肺结节和盆腔淋巴结可疑明显突出,先前 CT 上可疑为转移性扩散,但 FAPI 表达无增加;组织病理学排除了恶性肿瘤。
[Ga]Ga-FAPI-46 PET 在 UC 病变中显示出明显升高的摄取。因此,该示踪剂具有作为转移性 UC 患者有前途的新生物标志物的潜力,因为与单独 CT 相比,[Ga]Ga-FAPI-46 PET 可能提高对转移部位的检测。这些发现高度强调了在 UC 患者中进行 FAPI 成像的更大研究。