Atri Mostafa
Department of Medical Imaging, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
J Clin Oncol. 2006 Jul 10;24(20):3299-308. doi: 10.1200/JCO.2006.06.6159.
Molecular imaging represents tissue-specific imaging and quantification of physiologic (functional) and molecular events in tumors utilizing new noninvasive imaging modalities, radioligands, and contrast agents. It combines anatomic, physiologic, and metabolic information in a single imaging session. Molecular imaging relies on the ability to target genes and proteins that are linked directly or indirectly to human disease. New imaging biomarkers are being developed. In addition, functional and molecular imaging can potentially replace anatomic longitudinal studies by assessing treatment response earlier. Vascular targeting agents can be evaluated by imaging of tumor angiogenesis using magnetic resonance imaging (MRI), computed tomography and ultrasound, and positron emission tomography (PET). Targeted contrast agents can accomplish site-directed imaging or therapy by a variety of active and passive mechanisms. Furthermore, there is the possibility of combining different modalities such as ultrasonic imaging and MRI or MRI and PET to increase the flexibility unachievable with either modality alone. However, there is a need to standardize these techniques so that longitudinal evaluation of tumor response to treatment is feasible.
分子成像利用新的非侵入性成像方式、放射性配体和造影剂,对肿瘤中的生理(功能)和分子事件进行组织特异性成像和定量分析。它在一次成像过程中结合了解剖、生理和代谢信息。分子成像依赖于靶向直接或间接与人类疾病相关的基因和蛋白质的能力。新的成像生物标志物正在不断开发。此外,功能和分子成像通过更早地评估治疗反应,有可能取代解剖学纵向研究。血管靶向剂可通过使用磁共振成像(MRI)、计算机断层扫描、超声和正电子发射断层扫描(PET)对肿瘤血管生成进行成像来评估。靶向造影剂可通过多种主动和被动机制实现定点成像或治疗。此外,将不同的成像方式(如超声成像与MRI或MRI与PET)相结合,有可能增加单独使用任何一种方式都无法实现的灵活性。然而,需要对这些技术进行标准化,以便对肿瘤治疗反应进行纵向评估是可行的。