99mTc 标记肽在肿瘤成像中的临床应用:现状与未来方向

iRadiology Pub Date : 2024-01-21 DOI:10.1002/ird3.55
Jiyun Shi, Shuang Liu
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引用次数: 0

摘要

利用放射性标记肽靶向癌细胞上过度表达的受体已成为肿瘤学分子成像的一个重要方面。小肽由于体积小、放射性标记方案简单,具有靶向肿瘤、副作用和毒性最小的有利特性。其中,体生长抑素类似物已获得监管部门批准,用于诊断和治疗神经内分泌肿瘤。环状 RGD(Arg-Gly-Asp)肽、bombesin 类似物和胰高血糖素样肽-1 类似物目前正在开发和/或进行临床试验。最常用的肿瘤成像放射性核素包括用于单光子发射计算机断层扫描的 99mTc 和 111In,以及用于正电子发射断层扫描的 68Ga 和 18F。本综述重点介绍 99mTc 标记肽用于肿瘤成像的临床潜力和未来前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical application of 99mTc-labeled peptides for tumor imaging: Current status and future directions

Clinical application of 99mTc-labeled peptides for tumor imaging: Current status and future directions

Targeting receptors overexpressed on cancer cells with radiolabeled peptides has become a crucial aspect of molecular imaging in oncology. Small peptides offer favorable characteristics for tumor targeting with minimal side effects and toxicity owing to their small size and simple radiolabeling protocols. Among them, somatostatin analogs have received regulatory approval for the diagnosis and treatment of neuroendocrine tumors. Cyclic RGD (Arg-Gly-Asp) peptides, bombesin analogs, and glucagon-like peptide-1 analogs are currently under development and/or undergoing clinical trials. The most used radionuclides for tumor imaging include 99mTc and 111In for single-photon emission computed tomography, 68Ga and 18F for positron emission tomography. This review highlights the clinical potential and future prospects of 99mTc-labeled peptides for tumor imaging.

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