Higuchi Takahiro, Klimek Konrad, Groener Daniel, Chen Xinyu, Werner Rudolf A
Clinic for Radiology and Nuclear Medicine, Department of Nuclear Medicine, Goethe University Frankfurt, University Hospital, Frankfurt, Germany.
Nuclear Medicine, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Clin Nucl Med. 2025 Jan 1;50(1):44-51. doi: 10.1097/RLU.0000000000005567. Epub 2024 Nov 19.
In the evolving landscape of precision oncology, this review delineates the role of radiopharmaceuticals targeting the norepinephrine transporter (NET), with a particular focus on the current clinical application of 123 I-MIBG diagnostic imaging and 131 I-MIBG therapeutics, in particular for pheochromocytoma, neuroblastoma, or paraganglioma. We will also highlight recently introduced 18 F-labeled NET targeting imaging radiotracers, which would offer unparalleled resolution, enhanced tumor localization, and staging properties. Complementing these novel second-generation PET agents in a theranostic approach, astatine-211 meta-astatobenzylguanidine ( 211 At-MABG) would leverage the advantages of alpha-particles to selectively target and eradicate NET-expressing tumor cells with minimal off-target effects.
在精准肿瘤学不断发展的背景下,本综述阐述了靶向去甲肾上腺素转运体(NET)的放射性药物的作用,特别关注123I-MIBG诊断成像和131I-MIBG治疗的当前临床应用,尤其是针对嗜铬细胞瘤、神经母细胞瘤或副神经节瘤。我们还将重点介绍最近推出的靶向NET的18F标记成像放射性示踪剂,其具有无与伦比的分辨率、增强的肿瘤定位和分期特性。作为这些新型第二代PET药物在治疗诊断方法中的补充,砹-211间位-砹苄基胍(211At-MABG)将利用α粒子的优势,以最小的脱靶效应选择性地靶向并根除表达NET的肿瘤细胞。