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PSMA-1-多胺基多羧基大环配体 有望用于前列腺癌的有效靶向放射性配体治疗。

PSMA-1-DOTA Potentially for Effective Targeted Radioligand Therapy of Prostate Cancer.

作者信息

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

机构信息

Biomedical Engineering, Case Western Reserve University, Cleveland, OH, USA.

Radiology, Case Western Reserve University, Cleveland, OH, USA.

出版信息

Mol Imaging Biol. 2025 Sep 2. doi: 10.1007/s11307-025-02046-9.

Abstract

PURPOSE

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.

PROCEDURES

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

程序

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。

结果

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。

结论

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。

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