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PET 成像在转移性乳腺癌中的未来作用。

The Future Role of PET Imaging in Metastatic Breast Cancer.

机构信息

Department of Nuclear Medicine, University Hospital Essen, Essen, Germany.

West German Cancer Center, Heidelberg, Germany.

出版信息

Oncol Res Treat. 2022;45(1-2):18-25. doi: 10.1159/000521079. Epub 2021 Nov 24.

Abstract

BACKGROUND

A variety of therapeutic approaches are employed to treat patients suffering from breast cancer. Likewise, a broad spectrum of imaging ligands has been introduced for noninvasive positron emission tomography/computed tomography (PET/CT) imaging to enable comprehensive tumor characterization and more accurate response evaluation.

SUMMARY

In recent years, novel radioactively labeled ligands have been developed for PET/CT imaging in metastatic breast cancer. One promising tracer is [18F]fluoroestradiol, which was recently approved by the Food and Drug Administration. It can be used for a whole-body assessment of estrogen receptor status. Another radionuclide currently under development is [68Ga]Ga-fibroblast-activation-protein inhibitor. In addition to new radionuclides, the field of application for existing tracers like [18F]fluorodeoxyglucose (FDG) was broadened. It has been shown that an early therapeutic response to various therapies can be detected by [18F]FDG PET/CT, which leads to early treatment optimization. Key Message: In this review, we highlighted new tracers and applications of PET/CT imaging as well as therapeutic approaches in patients with advanced breast cancer. Furthermore, we give an outlook on the application of artificial intelligence, immunoPET, and liquid biopsy.

摘要

背景

目前有多种治疗方法可用于治疗乳腺癌患者。同样,也引入了广泛的成像配体,用于非侵入性正电子发射断层扫描/计算机断层扫描(PET/CT)成像,以实现全面的肿瘤特征描述和更准确的反应评估。

摘要

近年来,新型放射性标记配体已被开发用于转移性乳腺癌的 PET/CT 成像。一种很有前途的示踪剂是[18F]氟雌二醇,它最近获得了美国食品和药物管理局的批准。它可用于全身评估雌激素受体状态。另一种正在开发中的放射性核素是[68Ga]Ga-成纤维细胞激活蛋白抑制剂。除了新的放射性核素外,[18F]氟脱氧葡萄糖(FDG)等现有示踪剂的应用范围也有所扩大。研究表明,[18F]FDG PET/CT 可检测到各种治疗方法的早期治疗反应,从而实现早期治疗优化。

关键信息

在这篇综述中,我们强调了新型示踪剂以及 PET/CT 成像在晚期乳腺癌患者中的治疗方法的应用,并展望了人工智能、免疫 PET 和液体活检的应用。

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