Synthesis, preclinical assessment, and first-in-human study of [18F]d4-FET for brain tumor imaging.

IF 8.6 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Journal of Nuclear Medicine and Molecular Imaging Pub Date : 2024-11-01 DOI:10.1007/s00259-024-06964-8
Lu Hou, Zhiyong Chen, Fanfan Chen, Lianghe Sheng, Weijian Ye, Yingchu Dai, Xiaoyu Guo, Chenchen Dong, Guocong Li, Kai Liao, Yinlong Li, Jie Ma, Huiyi Wei, Wenqing Ran, Jingjie Shang, Xueying Ling, Jimmy S Patel, Steven H Liang, Hao Xu, Lu Wang
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引用次数: 0

Abstract

Purpose: Tumor-to-background ratio (TBR) is a critical metric in oncologic PET imaging. This study aims to enhance the TBR of [18F]FET in brain tumor imaging by substituting deuterium ("D") for hydrogen ("H"), thereby improving the diagnostic sensitivity and accuracy.

Methods: [18F]d4-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 [18F]d4-FET and [18F]FET, and two patients with brain metastases were imaged using [18F]d4-FET and [18F]FDG.

Results: [18F]d4-FET demonstrated high radiochemical purity and yield. PET/MRI in rodent models demonstrated superior TBR for [18F]d4-FET compared to [18F]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 [18F]FET. In glioma patients, [18F]d4-FET showed enhanced TBR, while in patients with brain metastases, [18F]d4-FET displayed superior lesion delineation compared to [18F]FDG, especially in smaller metastatic sites.

Conclusion: We successfully synthesized the novel PET radiotracer [18F]d4-FET, which retains the advantageous properties of [18F]FET while potentially enhancing TBR for glioma imaging. Preliminary studies indicate excellent stability, efficacy, and sensitivity of [18F]d4-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.

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用于脑肿瘤成像的[18F]d4-FET的合成、临床前评估和首次人体研究。
目的:肿瘤与背景比(TBR)是肿瘤 PET 成像的一个关键指标。本研究旨在通过用氘("D")代替氢("H")来提高[18F]FET 在脑肿瘤成像中的 TBR,从而提高诊断的灵敏度和准确性。方法:通过两个自动放射化学模块合成了[18F]d4-FET,并在啮齿动物模型体内和体外进行了生物分布研究和成像效果评估,同时在非人灵长类动物体内进行了代谢稳定性和辐射剂量评估。此外,还对五名脑肿瘤患者进行了初步成像评估:三名胶质瘤患者接受了[18F]d4-FET和[18F]FET成像,两名脑转移患者接受了[18F]d4-FET和[18F]FDG成像:结果:[18F]d4-FET 显示出很高的放射化学纯度和产量。在啮齿类动物模型中进行的 PET/MRI 显示,与[18F]FET 相比,[18F]d4-FET 的 TBR 更优越,自体放射成像显示肿瘤边缘与病理范围密切相关。对猴的研究表明,[18F]d4-FET 的体内稳定性和有效剂量与[18F]FET 相当。在胶质瘤患者中,[18F]d4-FET 显示出更强的 TBR,而在脑转移患者中,[18F]d4-FET 显示出比[18F]FDG 更好的病灶轮廓,尤其是在较小的转移部位:我们成功合成了新型 PET 放射性示踪剂[18F]d4-FET,它既保留了[18F]FET 的优势特性,又有可能提高胶质瘤成像的 TBR。初步研究表明,[18F]d4-FET 具有出色的稳定性、有效性和灵敏度,有望用于脑肿瘤的临床评估:ChiCTR2400081576,注册日期:2024-03-05,https://www.chictr.org.cn/bin/project/edit?pid=206162。
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来源期刊
CiteScore
15.60
自引率
9.90%
发文量
392
审稿时长
3 months
期刊介绍: The European Journal of Nuclear Medicine and Molecular Imaging serves as a platform for the exchange of clinical and scientific information within nuclear medicine and related professions. It welcomes international submissions from professionals involved in the functional, metabolic, and molecular investigation of diseases. The journal's coverage spans physics, dosimetry, radiation biology, radiochemistry, and pharmacy, providing high-quality peer review by experts in the field. Known for highly cited and downloaded articles, it ensures global visibility for research work and is part of the EJNMMI journal family.
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