nectin -4靶向PET显像剂68Ga-FZ-NR-1在三阴性乳腺癌中的初步研究

Li Sun, Yuyun Sun, Ke Zuo, Lei Fan, Xiao Wang, Jianping Zhang, Silong Hu, Xiaosheng Liu, Jindian Li, Ye Li, Zhiming Shao, Xiaoping Xu, Aiguo Wu, Shaoli Song
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引用次数: 0

摘要

Nectin细胞粘附分子4 (Nectin-4)是一种新兴的癌症诊断和治疗生物标志物。我们开发了一种以Nectin-4为靶点的68Ga-DOTA-Sar10-Nectin-4 (68Ga-FZ-NR-1) PET/CT示踪剂,用于检测肿瘤模型和三阴性乳腺癌(TNBC)患者中Nectin-4的表达。方法:合成一系列以nectin -4为靶点的放射性示踪剂68ga - fz - nr -1、68ga - dota -聚乙二醇5-Nectin-4 (68Ga-FZ-NR-2)和68ga - dota -聚乙二醇10-Nectin-4 (68Ga-FZ-NR-3),并对其体外和体内的靶向能力和特异性进行评价。在MDA-MB-468 (nectin -4阳性)和MDA-MB-231 (nectin -4阴性)细胞系中进行体外实验。对肿瘤模型进行PET/CT成像,以评估放射性示踪剂的nectin -4靶向能力。经过临床前实验和筛选,68Ga-FZ-NR-1放射性示踪剂在TNBC患者的首次人体试验中被选中进行安全性和有效性评估。阳性病变活检,免疫组化分析Nectin-4表达水平。结果:3个68ga标记的放射性示踪剂具有较高的放射化学纯度、稳定性和对Nectin-4的亲和力。体外细胞摄取研究表明,放射性示踪剂能有效靶向MDA-MB-468细胞中的Nectin-4,其中68Ga-FZ-NR-1靶向效果最高。在MDA-MB-468肿瘤模型中,PET/CT成像显示68Ga-FZ-NR-1的摄取率高于68Ga-FZ-NR-2和68Ga-FZ-NR-3,并表现出良好的药代动力学和安全性。68Ga-FZ-NR-1因此被选择用于后续的临床试验。68Ga-FZ-NR-1 PET/CT有效识别9例TNBC患者的肿瘤,18F-FDG PET/CT证实。肿瘤病变的活检样本显示,68Ga-FZ-NR-1 PET/CT鉴定的阳性病变对应于Nectin-4高表达区域。结论:研制并评价了一系列以nectin -4为靶点的放射性示踪剂(68Ga-FZ-NR-1、68Ga-FZ-NR-2、68Ga-FZ-NR-3)。临床前研究表明,68Ga-FZ-NR-1可以识别Nectin-4高表达的肿瘤。在初步临床研究中,使用68Ga-FZ-NR-1有效识别和可视化TNBC患者中表达nectin -4的肿瘤病变,免疫组织化学证实了这一点。这种放射性示踪剂为评估Nectin-4提供了一种无创方法,并为开发针对TNBC的Nectin-4靶向治疗提供了潜在的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pilot Study of Nectin-4-Targeted PET Imaging Agent 68Ga-FZ-NR-1 in Triple-Negative Breast Cancer from Bench to First-in-Human.

Nectin cell adhesion molecule 4 (Nectin-4) is an emerging biomarker for cancer diagnosis and therapy. We developed a Nectin-4-targeted 68Ga-DOTA-Sar10-Nectin-4 (68Ga-FZ-NR-1) PET/CT radiotracer for detecting Nectin-4 expression in a tumor model and in triple-negative breast cancer (TNBC) patients. Methods: A series of Nectin-4-targeted radiotracers-68Ga-FZ-NR-1, 68Ga-DOTA-polyethylene glycol 5-Nectin-4 (68Ga-FZ-NR-2), and 68Ga-DOTA-polyethylene glycol 10-Nectin-4 (68Ga-FZ-NR-3)-were synthesized, and their targeting ability and specificity were evaluated in vitro and in vivo. In vitro experiments were performed in the MDA-MB-468 (Nectin-4-positive) and MDA-MB-231 (Nectin-4-negative) cell lines. PET/CT imaging in tumor models was performed to assess the Nectin-4-targeting ability of the radiotracers. After preclinical experiments and screening, the 68Ga-FZ-NR-1 radiotracer was selected for safety and efficacy evaluation in a first-in-human trial in TNBC patients. Positive lesions were biopsied and analyzed by immunohistochemistry to determine Nectin-4 expression levels. Results: The 3 68Ga-labeled radiotracers exhibited high radiochemical purity, stability, and strong affinity for Nectin-4. In vitro cell uptake studies showed that the radiotracers effectively targeted Nectin-4 in MDA-MB-468 cells, and 68Ga-FZ-NR-1 showed the highest targeting efficacy. In the MDA-MB-468 tumor model, PET/CT imaging showed that 68Ga-FZ-NR-1 was taken up at higher rates than 68Ga-FZ-NR-2 and 68Ga-FZ-NR-3, and it exhibited favorable pharmacokinetics and safety profiles. 68Ga-FZ-NR-1 was thus selected for subsequent clinical trials. 68Ga-FZ-NR-1 PET/CT effectively identified tumors in 9 patients with TNBC, which was confirmed by 18F-FDG PET/CT. Biopsy samples of the tumor lesions revealed that the positive lesions identified by 68Ga-FZ-NR-1 PET/CT corresponded to areas of high Nectin-4 expression. Conclusion: A series of Nectin-4-targeted radiotracers (68Ga-FZ-NR-1, 68Ga-FZ-NR-2, and 68Ga-FZ-NR-3) was developed and evaluated. Preclinical studies demonstrated that 68Ga-FZ-NR-1 can identify tumors with high Nectin-4 expression. In a preliminary clinical study, 68Ga-FZ-NR-1 was used to effectively identify and visualize Nectin-4-expressing tumor lesions in patients with TNBC, which was confirmed by immunohistochemistry. This radiotracer provides a noninvasive approach to the assessment of Nectin-4 and a potential basis for the development of Nectin-4-targeted treatments for TNBC.

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