Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.
National Center for Tumor Diseases, Heidelberg, Germany.
J Nucl Med. 2020 Sep;61(9):1331-1336. doi: 10.2967/jnumed.119.237016. Epub 2020 Feb 14.
For oncologic management or radiotherapy planning, reliable staging tools are essential. The recent development of quinoline-based ligands targeting cancer-associated fibroblasts demonstrated promising preclinical and clinical results. The current study aimed to evaluate the role of fibroblast activation protein inhibitor (FAPI) PET/CT as a first clinical analysis for primary malignancies within the lower gastrointestinal tract (LGT). Ga-FAPI PET/CT was performed on a cohort of 22 patients with LGT tumors, including 15 patients with metastatic disease, 1 patient with suspected local relapse, and 6 treatment-naïve patients. Uptake of Ga-FAPI-04 and Ga-FAPI-46 was quantified by SUV and SUV After comparison with standard imaging, changes in tumor stage or localization and in oncologic or radiooncologic management were recorded. The highest uptake of FAPI tracer was observed in liver metastases and anal cancer, with an SUV of 9.1 and 13.9, respectively. Because of low background activity in normal tissue, there was a high tumor-to-background ratio of more than 3 in most lesions. In treatment-naïve patients, TNM was changed in 50%, whereas in patients with metastases, new findings occurred in 47%. In total, FAPI imaging caused a high, medium, and low change in oncologic or radiooncologic management in 19%, 33%, and 29%, respectively. For almost every patient undergoing irradiation, target volume delineation was improved by Ga-FAPI PET/CT. The present study demonstrated that both primary and metastatic LGT tumors were reliably detected by Ga-FAPI PET/CT, leading to relevant changes in TNM status and oncologic or radiooncologic management. Ga-FAPI PET/CT seems to be a highly promising imaging agent for the diagnosis and management of LGT tumors, potentially opening new applications for tumor staging or restaging.
对于肿瘤学管理或放射治疗计划,可靠的分期工具至关重要。最近开发的针对癌相关成纤维细胞的喹啉基配体显示出有前途的临床前和临床结果。本研究旨在评估成纤维细胞激活蛋白抑制剂(FAPI)PET/CT 在评估下消化道(LGT)原发性恶性肿瘤中的作用。对 22 例 LGT 肿瘤患者进行 Ga-FAPI PET/CT 检查,其中 15 例为转移性疾病患者,1 例为局部复发可疑患者,6 例为未经治疗的患者。通过 SUV 和 SUV 定量测定 Ga-FAPI-04 和 Ga-FAPI-46 的摄取量。与标准成像相比,记录肿瘤分期或定位的变化以及肿瘤学或放射肿瘤学管理的变化。FAPI 示踪剂的摄取最高见于肝转移和肛门癌,SUV 分别为 9.1 和 13.9。由于正常组织的背景活性低,大多数病变的肿瘤与背景比超过 3。在未经治疗的患者中,TNM 改变了 50%,而在转移患者中,新发现占 47%。总的来说,FAPI 成像导致肿瘤学或放射肿瘤学管理的高、中、低改变分别为 19%、33%和 29%。对于几乎每一位接受照射的患者,靶区勾画都因 Ga-FAPI PET/CT 而得到改善。本研究表明,Ga-FAPI PET/CT 可靠地检测原发性和转移性 LGT 肿瘤,导致 TNM 状态和肿瘤学或放射肿瘤学管理的相关变化。Ga-FAPI PET/CT 似乎是一种很有前途的 LGT 肿瘤诊断和管理成像剂,可能为肿瘤分期或再分期开辟新的应用。