Department of Radiation Medicine, Oregon Health & Science University, Portland, Oregon 97239, USA.
Acta Oncol. 2010 Oct;49(7):948-55. doi: 10.3109/0284186X.2010.510533.
The use of positron emission tomography (PET) using F18 labeled fluorodeoxyglucose (FDG) for both oncology disease staging and radiation therapy target volume delineation has steadily increased over the last decade, and FDG-PET is today readily available in all major medical centers. The goal of anti tumor treatment, including chemotherapy and/or radiation therapy is to diminish a tumor cell population, ideally to the state of total eradication. Reducing the number of viable tumor cells can lead to a reduction in anatomical tumor size, and may also be correlated with decreased FDG uptake. Efforts to assess tumor response to therapy have attempted to describe and quantify changes in glucose utilization, also referred to as metabolic tumor response. In this review, an attempt is made to present and discuss methodologies to assess and quantify tumor metabolic response to radiation therapy or chemoradiation treatment courses.
过去十年间,正电子发射断层扫描(PET)联合 F18 标记氟脱氧葡萄糖(FDG)在肿瘤疾病分期和放射治疗靶区勾画中的应用稳步增加,目前所有主要医疗中心都可方便地获得 FDG-PET。抗肿瘤治疗(包括化疗和/或放疗)的目标是减少肿瘤细胞群体,理想情况下达到完全消除的状态。降低存活肿瘤细胞的数量可导致解剖学肿瘤大小缩小,并且可能与 FDG 摄取减少相关。评估肿瘤对治疗的反应的努力尝试描述和量化葡萄糖利用的变化,也称为代谢肿瘤反应。在本综述中,尝试提出并讨论评估和量化肿瘤对放射治疗或放化疗治疗过程的代谢反应的方法。