68Ga-FAPI PET/CT在恶性肿瘤中的临床应用

Clinical application of 68Ga-FAPI PET/CT in malignant tumors

  • 摘要: 成纤维细胞激活蛋白(FAP)作为肿瘤相关成纤维细胞(CAFs)的分子标志物之一,在激活的CAFs中高度特异性表达。FAP具有促进肿瘤侵袭、转移和免疫逃逸的作用,可作为恶性肿瘤诊疗的重要靶点。镓-68标记的FAP抑制剂(68Ga-FAPI)是基于FAP合成的小分子探针,经PET/CT显像可实现FAP在体内的可视化。目前,68Ga-FAPI PET/CT已成功应用于神经胶质瘤、食管癌、肝细胞癌和胰腺导管腺癌等恶性肿瘤的诊断和分期。笔者综述了68Ga-FAPI PET/CT在恶性肿瘤中的临床应用情况。

     

    Abstract: Fibroblast activation protein (FAP), as one of the molecular markers of cancer-associated fibroblasts (CAFs), is highly specifically expressed in activated CAFs. FAP can be used as a theranostic target for malignant tumors since it can promote tumor invasion, metastasis and immune escape. Gallium-68-labeled FAP inhibitor (68Ga-FAPI) is a small molecular probe synthesized based on FAP, which can be visualized in vivo by PET/CT imaging. At present, 68Ga-FAPI PET/CT has been successfully used in the diagnosis and staging of glioma, esophageal cancer, hepatocellular carcinoma, pancreatic ductal adenocarcinoma and other malignant tumors. This paper reviews the clinical application of 68Ga-FAPI PET/CT in malignant tumors.

     

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