Molecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Semin Oncol. 2011 Feb;38(1):70-86. doi: 10.1053/j.seminoncol.2010.11.005.
Positron emission tomography (PET) is one of the most rapidly growing areas of medical imaging, with many applications in the clinical management of patients with cancer. The principal goal of PET imaging is to visualize, characterize, and measure biological processes at the cellular, subcellular, and molecular levels in living subjects using noninvasive procedures. PET imaging takes advantage of the traditional diagnostic imaging techniques and introduces positron-emitting probes to determine the expression of indicative molecular targets at different stages of cancer progression. Although [(18)F]fluorodeoxyglucose ([(18)F]FDG)-PET has been widely utilized for staging and restaging of cancer, evaluation of response to treatment, differentiation of post-therapy alterations from residual or recurrent tumor, and assessment of prognosis, [(18)F]FDG is not a target-specific PET tracer. Over the last decade, numerous target-specific PET tracers have been developed and evaluated in preclinical and clinical studies. This review provides an overview of the current status and trends in the development of non-[(18)F]FDG PET probes in oncology and their application in the investigation of cancer biology.
正电子发射断层扫描(PET)是医学影像学中发展最快的领域之一,在癌症患者的临床管理中有许多应用。PET 成像的主要目标是使用非侵入性程序在活体内可视化、描绘和测量细胞、亚细胞和分子水平的生物过程。PET 成像利用传统的诊断成像技术,并引入正电子发射探针来确定在癌症进展的不同阶段指示性分子靶标的表达。尽管[(18)F]氟脱氧葡萄糖([(18)F]FDG)-PET 已广泛用于癌症的分期和再分期、治疗反应的评估、治疗后改变与残留或复发性肿瘤的区分以及预后评估,但[(18)F]FDG 不是靶向特异性 PET 示踪剂。在过去的十年中,已经在临床前和临床研究中开发和评估了许多靶向特异性 PET 示踪剂。本综述概述了肿瘤学中非[(18)F]FDG PET 探针的发展现状和趋势及其在癌症生物学研究中的应用。