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用于脑肿瘤成像的[F]d-FET的合成、临床前评估及首次人体研究。

Synthesis, preclinical assessment, and first-in-human study of [F]d-FET for brain tumor imaging.

作者信息

Hou Lu, Chen Zhiyong, Chen Fanfan, Sheng Lianghe, Ye Weijian, Dai Yingchu, Guo Xiaoyu, Dong Chenchen, Li Guocong, Liao Kai, Li Yinlong, Ma Jie, Wei Huiyi, Ran Wenqing, Shang Jingjie, Ling Xueying, Patel Jimmy S, Liang Steven H, Xu Hao, Wang Lu

机构信息

Center of Cyclotron and PET Radiopharmaceuticals, Department of Nuclear Medicine, & Key Laboratory of Basic and Translational Research On Radiopharmaceuticals, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.

Department of Neurosurgery, The First Affiliated Hospital of Jinan University, Guangzhou, 510630, China.

出版信息

Eur J Nucl Med Mol Imaging. 2025 Feb;52(3):864-875. doi: 10.1007/s00259-024-06964-8. Epub 2024 Nov 1.

Abstract

PURPOSE

Tumor-to-background ratio (TBR) is a critical metric in oncologic PET imaging. This study aims to enhance the TBR of [F]FET in brain tumor imaging by substituting deuterium ("D") for hydrogen ("H"), thereby improving the diagnostic sensitivity and accuracy.

METHODS

[F]d-FET was synthesised by two automated radiochemistry modules. Biodistribution studies and imaging efficacy were evaluated in vivo  and ex vivo in rodent models, while metabolic stability and radiation dosimetry were assessed in non-human primates. Additionally, preliminary imaging evaluations were carried out in five brain tumor patients: three glioma patients underwent imaging with both [F]d-FET and [F]FET, and two patients with brain metastases were imaged using [F]d-FET and [F]FDG.

RESULTS

[F]d-FET demonstrated high radiochemical purity and yield. PET/MRI in rodent models demonstrated superior TBR for [F]d-FET compared to [F]FET, and autoradiography showed tumor margins that correlated well with pathological extents. Studies in cynomolgus monkeys indicated comparable in vivo stability and effective dose with [F]FET. In glioma patients, [F]d-FET showed enhanced TBR, while in patients with brain metastases, [F]d-FET displayed superior lesion delineation compared to [F]FDG, especially in smaller metastatic sites.

CONCLUSION

We successfully synthesized the novel PET radiotracer [F]d-FET, which retains the advantageous properties of [F]FET while potentially enhancing TBR for glioma imaging. Preliminary studies indicate excellent stability, efficacy, and sensitivity of [F]d-FET, suggesting its potential in clinical evaluations of brain tumors.

TRIAL REGISTRATION

ChiCTR2400081576, registration date: 2024-03-05, https://www.chictr.org.cn/bin/project/edit?pid=206162.

摘要

目的

肿瘤与本底比值(TBR)是肿瘤PET成像中的关键指标。本研究旨在通过用氘(“D”)取代氢(“H”)来提高[F]FET在脑肿瘤成像中的TBR,从而提高诊断敏感性和准确性。

方法

[F]d-FET由两个自动化放射化学模块合成。在啮齿动物模型中进行了体内和体外的生物分布研究及成像效能评估,同时在非人类灵长类动物中评估了代谢稳定性和辐射剂量学。此外,对5例脑肿瘤患者进行了初步成像评估:3例胶质瘤患者接受了[F]d-FET和[F]FET的成像,2例脑转移瘤患者使用[F]d-FET和[F]FDG进行成像。

结果

[F]d-FET显示出高放射化学纯度和产率。啮齿动物模型中的PET/MRI显示,与[F]FET相比,[F]d-FET的TBR更高,放射自显影显示肿瘤边缘与病理范围相关性良好。食蟹猴研究表明,[F]d-FET在体内稳定性和有效剂量方面与[F]FET相当。在胶质瘤患者中,[F]d-FET显示TBR增强,而在脑转移瘤患者中,与[F]FDG相比,[F]d-FET在病变勾画方面表现更优,尤其是在较小的转移部位。

结论

我们成功合成了新型PET放射性示踪剂[F]d-FET,它保留了[F]FET的有利特性,同时可能提高胶质瘤成像的TBR。初步研究表明,[F]d-FET具有出色的稳定性、效能和敏感性,提示其在脑肿瘤临床评估中的潜力。

试验注册

ChiCTR2400081576,注册日期:2024年3月5日,https://www.chictr.org.cn/bin/project/edit?pid=206162。

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