Mankoff D A, Dehdashti F, Shields A F
Department of Radiology, University of Washington, Seattle, USA.
Neoplasia. 2000 Jan-Apr;2(1-2):71-88. doi: 10.1038/sj.neo.7900075.
Treatment decisions in oncology are increasingly guided by information on the biologic characteristics of tumors. Currently, patient-specific information on tumor biology is obtained from the analysis of biopsy material. Positron emission tomography (PET) provides quantitative estimates of regional biochemistry and receptor status and can overcome the sampling error and difficulty in performing serial studies inherent with biopsy. Imaging using the glucose metabolism tracer, 2 -deoxy-2- fluoro-D-glucose (FDG), has demonstrated PET's ability to guide therapy in clinical oncology. In this review, we highlight PET approaches to imaging two other aspects of tumor biology: cellular proliferation and tumor steroid receptors. We review the biochemical and biologic processes underlying the imaging, positron-emitting radiopharmaceuticals that have been developed, quantitative image-analysis considerations, and clinical studies to date. This provides a basis for evaluating future developments in these promising applications of PET metabolic imaging.
肿瘤学中的治疗决策越来越多地受到肿瘤生物学特征信息的指导。目前,关于肿瘤生物学的患者特异性信息是通过对活检材料的分析获得的。正电子发射断层扫描(PET)可提供区域生物化学和受体状态的定量估计,并且能够克服活检固有的采样误差以及进行系列研究的困难。使用葡萄糖代谢示踪剂2-脱氧-2-氟-D-葡萄糖(FDG)进行成像,已证明PET在临床肿瘤学中具有指导治疗的能力。在本综述中,我们重点介绍PET用于对肿瘤生物学的另外两个方面进行成像的方法:细胞增殖和肿瘤类固醇受体。我们回顾了成像背后的生化和生物学过程、已开发的正电子发射放射性药物、定量图像分析注意事项以及迄今为止的临床研究。这为评估PET代谢成像这些有前景的应用中的未来发展提供了基础。