Preclinical Evaluation and a Pilot Clinical Positron Emission Tomography Imaging Study of [<sup>68</sup>Ga]Ga-FAPI-FUSCC-II
Xinyue Du, Bingxin Gu, Xiao Wang, Xiangwei Wang, Mengjing Ji, Jianping Zhang, Simin He, Xiaoping Xu, Zhongyi Yang, Shaoli Song
Abstract
Fibroblast activation protein (FAP), a type II integral membrane serine protease, is a promising target for tumor diagnosis and therapy. OncoFAP has been recently discovered for PET imaging procedures for various solid malignancies. In this study, we presented the development of manual radiolabeling procedures for the preparation of OncoFAP-based radiopharmaceuticals for cancer imaging. A novel series of [ 68 Ga/ 177 Lu]Ga/Lu-FAPI-FUSCC-I/II were produced with high radiochemical yields. [ 68 Ga]Ga-FAPI-FUSCC-I/II and [ 177 Lu]Lu-FAPI-FUSCC-I/II were stable in phosphate-buffered saline, fetal bovine serum, and human serum for at least 3 h. In vitro cellular uptake and blocking experiments implied that they had specificity to FAP. Additionally, the low nanomolar IC 50 values of FAPI-FUSCC-II indicated that it had a high target affinity to FAP. The in vivo biodistribution and blocking study in mice bearing HT-1080-FAP tumors showed that both exhibited specific tumor uptake. [ 68 Ga]Ga-FAPI-FUSCC-II showed a higher tumor uptake and a higher tumor/nontarget ratio than [ 68 Ga]Ga-FAPI-FUSCC-I and [ 68 Ga]Ga-FAPI-04. The results of ex vivo biodistribution were in accordance with the biodistribution results. Clinical [ 68 Ga]Ga-FAPI-FUSCC-II-PET/CT imaging further demonstrated its favorable biodistribution and kinetics with elevated and reliable uptake by primary tumors (maximum standardized uptake value (SUV max ), 12.17 ± 6.67) and distant metastases (SUV max, 9.24 ± 4.28). In summary, [ 68 Ga]Ga-FAPI-FUSCC-II displayed increased tumor uptake and retention compared to [ 68 Ga]Ga-FAPI-04, giving it potential as a promising tracer for the diagnostic imaging of malignant tumors with positive FAP expression.