Waldman Adam D, Jackson Alan, Price Stephen J, Clark Christopher A, Booth Thomas C, Auer Dorothee P, Tofts Paul S, Collins David J, Leach Martin O, Rees Jeremy H
Department of Imaging, Imperial College, London, UK.
Nat Rev Clin Oncol. 2009 Aug;6(8):445-54. doi: 10.1038/nrclinonc.2009.92. Epub 2009 Jun 23.
Conventional structural imaging provides limited information on tumor characterization and prognosis. Advances in neurosurgical techniques, radiotherapy planning and novel drug treatments for brain tumors have generated increasing need for reproducible, noninvasive, quantitative imaging biomarkers. This Review considers the role of physiological MRI and PET molecular imaging in understanding metabolic processes associated with tumor growth, blood flow and ultrastructure. We address the utility of various techniques in distinguishing between tumors and non-neoplastic processes, in tumor grading, in defining anatomical relationships between tumor and eloquent brain regions and in determining the biological substrates of treatment response. Much of the evidence is derived from limited case series in individual centers. Despite their 'added value', the effect of these techniques as an adjunct to structural imaging in clinical research and practice remains limited.
传统的结构成像在肿瘤特征描述和预后方面提供的信息有限。神经外科技术、放射治疗计划以及脑肿瘤新型药物治疗的进展,使得对可重复、无创、定量成像生物标志物的需求日益增加。本综述探讨了生理磁共振成像(MRI)和正电子发射断层扫描(PET)分子成像在理解与肿瘤生长、血流及超微结构相关的代谢过程中的作用。我们阐述了各种技术在区分肿瘤与非肿瘤性病变、肿瘤分级、确定肿瘤与明确脑区之间的解剖关系以及确定治疗反应的生物学基础方面的效用。大部分证据来自各个中心的有限病例系列。尽管这些技术具有“附加价值”,但在临床研究和实践中,它们作为结构成像辅助手段的作用仍然有限。