GDMPA Key Laboratory for Quality Control and Evaluation of Radiopharmaceuticals, Department of Nuclear Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province 510515, China.
Department of Nuclear Medicine, The Tenth Affiliated Hospital of Southern Medical University (Dongguan People's Hospital), Dongguan 523059, P. R. China.
J Med Chem. 2024 Oct 10;67(19):17785-17795. doi: 10.1021/acs.jmedchem.4c01812. Epub 2024 Sep 25.
Fibroblast activation protein (FAP) is specifically expressed on cancer-associated fibroblasts in over 90% of tumors and is considered a promising target for cancer theranostics. Here, we developed a novel tracer, DOTA-FAPT, and labeled it with gallium-68 and lutetium-177 as a theranostic pair. [Ga]Ga/[Lu]Lu-FAPT exhibited high stability and hydrophilicity, as well as strong affinity to the FAP target. Micro-PET/CT imaging revealed that [Ga]Ga-FAPT exhibited significantly increased uptake in tumors and extended retention in A549-FAP and U87MG tumor xenografts as compared to [Ga]Ga-FAPI-04, demonstrating favorable pharmacokinetic characteristics in vivo. Therapeutic studies showed that [Lu]Lu-FAPT had higher tumor accumulation compared to [Lu]Lu-FAPI-04, leading to stronger tumor growth inhibition. The first-in-human evaluation also revealed that [Ga]Ga-FAPT has good in vivo distribution and superior diagnostic efficacy on primary and lymph node metastases in a patient with lung cancer. Our encouraging results suggest that Ga/Lu-labeled DOTA-FAPT is a theranostic pair with broad application prospect.
成纤维细胞激活蛋白(FAP)在超过 90%的肿瘤中特异性表达于癌相关成纤维细胞,被认为是癌症治疗学的有前途的靶点。在这里,我们开发了一种新型示踪剂 DOTA-FAPT,并将其用镓-68 和镥-177 标记为治疗学配对物。[Ga]Ga/[Lu]Lu-FAPT 表现出高稳定性和亲水性,以及对 FAP 靶标的强亲和力。Micro-PET/CT 成像显示,与 [Ga]Ga-FAPI-04 相比,[Ga]Ga-FAPT 在肿瘤中的摄取显著增加,并且在 A549-FAP 和 U87MG 肿瘤异种移植中的保留时间延长,显示出良好的体内药代动力学特征。治疗研究表明,与 [Lu]Lu-FAPI-04 相比,[Lu]Lu-FAPT 具有更高的肿瘤积累,导致更强的肿瘤生长抑制。首例人体评估还表明,[Ga]Ga-FAPT 在肺癌患者的原发性和淋巴结转移中具有良好的体内分布和优越的诊断效果。我们令人鼓舞的结果表明,Ga/Lu 标记的 DOTA-FAPT 是一种具有广泛应用前景的治疗学配对物。