First-in-human evaluation of four novel PSMA-targeted PET radiotracers with non-canonical amino acid linkage: A comparative study

作者：Dong Dai, Xin Gao, Siqi Zhang, Hongyi Huang, Kun Wang, Jianjing Liu, Xingkai Wang, Yuan Miao, Zongxiao Liu, Panfeng Li, Qingshuang Lu, Shuo Jiang, Xueyao Chen, Licheng Yang, Yiliang Li, Rui Wang, Y.‐W. ZHANG, Kuan Hu · 发表于：Pharmacological Research · 年份：2026 · DOI：10.1016/j.phrs.2026.108138 · 被引用次数：3 · 研究领域：Prostate Cancer Treatment and Research、Radiopharmaceutical Chemistry and Applications、Peptidase Inhibition and Analysis

PSMA-targeted radiopharmaceuticals have substantially advanced the management of prostate cancer; however, high nonspecific uptake in organs such as salivary glands and kidneys remains a clinical challenge. In previous studies, incorporation of non-canonical amino acid linkers was shown to reduce off-target uptake while preserving or even enhancing tumor accumulation of PSMA-targeted radiotracers. Here, we present a first-in-human head-to-head comparison of four linker-optimized PSMA radiotracers—[ 68 Ga]Ga-PSMA-HK4, [ 68 Ga]Ga-PSMA-HK7, [ 68 Ga]Ga-PSMA-Y55, and [ 68 Ga]Ga-PSMA-Y81—evaluating their in vivo pharmacokinetics and diagnostic performance in eight prostate cancer patients, with [ 68 Ga]Ga-PSMA-617 or [ 68 Ga]Ga-PSMA-11 serving as references. Preclinical data demonstrated that all four radiotracers achieved comparable or enhanced tumor uptake, with [ 68 Ga]Ga-PSMA-Y55 and [ 68 Ga]Ga-PSMA-Y81 showing reduced renal accumulation relative to [ 68 Ga]Ga-PSMA-617. Clinically, [ 68 Ga]Ga-PSMA-HK4 and [ 68 Ga]Ga-PSMA-HK7 exhibited lower salivary gland uptake, whereas [ 68 Ga]Ga-PSMA-Y55 and [ 68 Ga]Ga-PSMA-Y81 showed decreased renal retention compared with reference tracers. Tumor uptake of [ 68 Ga]Ga-PSMA-HK4 and [ 68 Ga]Ga-PSMA-Y55 was comparable to [ 68 Ga]Ga-PSMA-617, while [ 68 Ga]Ga-PSMA-HK7 and [ 68 Ga]Ga-PSMA-Y81 displayed prolonged blood pool and cardiac retention. These findings indicate that β 3 -amino acid linkers effectively reduced salivary gland uptake, while...