Department of Nuclear Medicine, University Hospital Heidelberg, Heidelberg, Germany.
Clinical Cooperation Unit Nuclear Medicine, German Cancer Research Center, Heidelberg, Germany.
J Nucl Med. 2021 Feb;62(2):160-167. doi: 10.2967/jnumed.120.244806. Epub 2020 Oct 30.
Fibroblast activation protein (FAP), a membrane-anchored peptidase, is highly expressed in cancer-associated fibroblasts in more than 90% of epithelial tumors and contributes to progression and worse prognosis of different cancers. Therefore, FAP is considered a promising target for radionuclide-based approaches for diagnosis and treatment of tumors and for the diagnosis of nonmalignant diseases associated with a remodeling of the extracellular matrix. Accordingly, a variety of quinolone-based FAP inhibitors (FAPIs) coupled to chelators were developed displaying specific binding to human and murine FAP with a rapid and almost complete internalization. Because of a high tumor uptake and a very low accumulation in normal tissues, as well as a rapid clearance from the circulation, a high contrast is obtained for FAPI PET/CT imaging even at 10 min after tracer administration. Moreover, FAPI PET/CT provides advantages over F-FDG PET/CT in several tumor entities for initial staging and detection of tumor recurrence and metastases, including peritonitis carcinomatosa.
成纤维细胞激活蛋白(FAP)是一种膜锚定肽酶,在超过 90%的上皮肿瘤相关的成纤维细胞中高度表达,并促进不同癌症的进展和预后不良。因此,FAP 被认为是基于放射性核素的肿瘤诊断和治疗方法以及与细胞外基质重塑相关的非恶性疾病诊断的有前途的靶点。相应地,已经开发了多种与螯合剂偶联的基于喹诺酮的 FAP 抑制剂(FAPIs),显示出与人和鼠 FAP 的特异性结合,具有快速且几乎完全的内化。由于肿瘤摄取率高,正常组织积累率非常低,以及从循环中快速清除,即使在示踪剂给药后 10 分钟,FAPI PET/CT 成像也能获得高对比度。此外,FAPI PET/CT 在初始分期、检测肿瘤复发和转移(包括癌性腹膜炎)方面优于 F-FDG PET/CT,在几种肿瘤实体中具有优势。