Wang Xinning, Sergeeva Olga, Sergeev Maxim, Zhang Lifang, Lockwood Zoey, Wojtylak Patrick, Sangster Riley, Reichert David, Berridge Marc, Weber Wolfgang, Lee Zhenghong, Basilion James P
Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.
Radiology, Case Western Reserve University, Cleveland, OH, USA.
Mol Imaging Biol. 2025 Sep 2. doi: 10.1007/s11307-025-02046-9.
While PSMA-targeted radioligand therapy (RLT) has shown remarkable efficacy for treating end-stage prostate cancer, the α-emitting RLT often results in severe salivary gland toxicity, limiting its use. Various strategies to mitigate this side effect have been attempted with limited success. Accordingly, this study introduced a new PSMA-targeting ligand with more favorable binding characteristics than the existing ligands.
The binding affinity of PSMA-1-DOTA to PSMA was compared with that of PSMA-11 and PSMA I&T. Comparison of uptake in the salivary glands, kidneys and PC3pip tumor cells in the xenograft mouse models between [ Ga]Ga-PSMA-1-DOTA, [ Ga]Ga-PSMA-11 and [ Ga]Ga-PSMA I&T was conducted with microPET/CT within the same week. The same mouse models were treated with [Lu]Lu-PSMA-1-DOTA or [Lu]Lu-PSMA-617. A compassionate use PET imaging study on a patient with metastatic castration-resistant prostate cancer was performed using [ Ga]Ga-PSMA-1-DOTA.
The binding affinity of PSMA-1-DOTA to PSMA was found to be approximately four times greater than other PSMA-targeted ligands. Imaging with microPET/CT revealed significantly lower kidney, uptake and little salivary and lacrimal gland uptake with [ Ga]Ga-PSMA-1-DOTA compared to other PSMA-radioligands. Preclinical efficacy studies demonstrated that [Lu]Lu-PSMA-1-DOTA inhibited tumor growth comparable to that with [Lu]Lu-PSMA-617, suggesting its potential to enhance the therapeutic window of targeted RLT by avoiding damage to the salivary glands. The compassionate use PET imaging confirmed the reduced salivary gland uptake of [ Ga]Ga-PSMA-1-DOTA in the patient, indicating its potential utility as a targeting agent for RLT with α- or β-emitting radionuclides in patients with PSMA-positive prostate cancer.
PSMA-1-DOTA shows reduced uptake in salivary glands while effectively targeting PSMA-expressing tumors, thus potentially avoiding the side effects of xerostomia, and possibly moving PSMA-targeted RLT to a more frontline therapy for prostate cancer rather than the current use as a last resort.
虽然靶向前列腺特异性膜抗原(PSMA)的放射性配体疗法(RLT)已显示出治疗晚期前列腺癌的显著疗效,但发射α粒子的RLT常导致严重的唾液腺毒性,限制了其应用。人们尝试了各种减轻这种副作用的策略,但成效有限。因此,本研究引入了一种新的靶向PSMA的配体,其结合特性比现有配体更有利。
将PSMA-1-DOTA与PSMA的结合亲和力与PSMA-11和PSMA I&T的进行比较。在同一周内,利用微型正电子发射断层扫描/计算机断层扫描(microPET/CT)对[镓]Ga-PSMA-1-DOTA、[镓]Ga-PSMA-11和[镓]Ga-PSMA I&T在异种移植小鼠模型的唾液腺、肾脏和PC3pip肿瘤细胞中的摄取情况进行比较。用[镥]Lu-PSMA-1-DOTA或[镥]Lu-PSMA-617对相同的小鼠模型进行治疗。使用[镓]Ga-PSMA-1-DOTA对一名转移性去势抵抗性前列腺癌患者进行了同情用药PET成像研究。
发现PSMA-1-DOTA与PSMA的结合亲和力比其他靶向PSMA的配体高约四倍。与其他PSMA放射性配体相比,microPET/CT成像显示,[镓]Ga-PSMA-1-DOTA的肾脏摄取显著降低,唾液腺和泪腺摄取极少。临床前疗效研究表明,[镥]Lu-PSMA-1-DOTA抑制肿瘤生长的效果与[镥]Lu-PSMA-617相当,这表明它有可能通过避免对唾液腺的损伤来扩大靶向RLT的治疗窗口。同情用药PET成像证实了患者唾液腺对[镓]Ga-PSMA-1-DOTA的摄取减少,表明它有可能作为一种靶向剂用于PSMA阳性前列腺癌患者的发射α或β粒子的放射性核素RLT。
PSMA-1-DOTA在有效靶向表达PSMA的肿瘤的同时,唾液腺摄取减少,从而有可能避免口干的副作用,并可能使靶向PSMA的RLT成为前列腺癌更前沿的治疗方法,而不是目前作为最后的手段使用。