Lee Yongsook C, Fullerton Gary D, Goins Beth A
Department of Radiation Oncology, University of Kansas School of Medicine.
J Vis Exp. 2013 Jul 29(77):50403. doi: 10.3791/50403.
World Health Organization (WHO) and the Response Evaluation Criteria in Solid Tumors (RECIST) working groups advocated standardized criteria for radiologic assessment of solid tumors in response to anti-tumor drug therapy in the 1980s and 1990s, respectively. WHO criteria measure solid tumors in two-dimensions, whereas RECIST measurements use only one-dimension which is considered to be more reproducible (1, 2, 3,4,5). These criteria have been widely used as the only imaging biomarker approved by the United States Food and Drug Administration (FDA) (6). In order to measure tumor response to anti-tumor drugs on images with accuracy, therefore, a robust quality assurance (QA) procedures and corresponding QA phantom are needed. To address this need, the authors constructed a preclinical multimodality (for ultrasound (US), computed tomography (CT) and magnetic resonance imaging (MRI)) phantom using tissue-mimicking (TM) materials based on the limited number of target lesions required by RECIST by revising a Gammex US commercial phantom (7). The Appendix in Lee et al. demonstrates the procedures of phantom fabrication (7). In this article, all protocols are introduced in a step-by-step fashion beginning with procedures for preparing the silicone molds for casting tumor-simulating test objects in the phantom, followed by preparation of TM materials for multimodality imaging, and finally construction of the preclinical multimodality QA phantom. The primary purpose of this paper is to provide the protocols to allow anyone interested in independently constructing a phantom for their own projects. QA procedures for tumor size measurement, and RECIST, WHO and volume measurement results of test objects made at multiple institutions using this QA phantom are shown in detail in Lee et al. (8).
世界卫生组织(WHO)和实体瘤疗效评价标准(RECIST)工作组分别在20世纪80年代和90年代倡导了用于评估实体瘤对抗肿瘤药物治疗反应的放射学评估标准化标准。WHO标准在二维上测量实体瘤,而RECIST测量仅使用一维,这被认为更具可重复性(参考文献1、2、3、4、5)。这些标准已被广泛用作美国食品药品监督管理局(FDA)批准的唯一影像生物标志物(参考文献6)。因此,为了在图像上准确测量肿瘤对抗肿瘤药物的反应,需要强大的质量保证(QA)程序和相应的QA体模。为满足这一需求,作者通过修改一款Gammex超声商业体模,基于RECIST要求的有限数量的靶病灶,使用仿组织(TM)材料构建了一种临床前多模态(用于超声(US)、计算机断层扫描(CT)和磁共振成像(MRI))体模(参考文献7)。Lee等人的附录展示了体模制作过程(参考文献7)。在本文中,所有方案均按步骤介绍,首先是为在体模中铸造肿瘤模拟测试对象准备硅胶模具的步骤,接着是用于多模态成像的TM材料的制备,最后是临床前多模态QA体模的构建。本文的主要目的是提供方案,使任何有兴趣的人都能为自己的项目独立构建体模。Lee等人详细展示了使用该QA体模在多个机构进行的测试对象的肿瘤大小测量的QA程序以及RECIST、WHO和体积测量结果(参考文献8)。