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本文引用的文献

1
Preclinical multimodality phantom design for quality assurance of tumor size measurement.用于肿瘤大小测量质量保证的临床前多模态体模设计
BMC Med Phys. 2011 Sep 30;11:1. doi: 10.1186/1756-6649-11-1.
2
QA procedures for multimodality preclinical tumor drug response testing.多模态临床前肿瘤药物反应测试的 QA 程序。
Med Phys. 2010 Sep;37(9):4806-16. doi: 10.1118/1.3464491.
3
New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1).实体瘤新的疗效评价标准:修订的RECIST指南(第1.1版)
Eur J Cancer. 2009 Jan;45(2):228-47. doi: 10.1016/j.ejca.2008.10.026.
4
Quantitative imaging biomarkers in the clinical development of targeted therapeutics: current and future perspectives.靶向治疗临床开发中的定量成像生物标志物:现状与未来展望。
Lancet Oncol. 2008 Aug;9(8):766-76. doi: 10.1016/S1470-2045(08)70196-7.
5
Radiologic measurements of tumor response to treatment: practical approaches and limitations.肿瘤治疗反应的放射学测量:实用方法与局限性
Radiographics. 2008 Mar-Apr;28(2):329-44. doi: 10.1148/rg.282075068.
6
RECIST revisited: a review of validation studies on tumour assessment.《实体瘤疗效评价标准》再探讨:肿瘤评估验证研究综述
Eur J Cancer. 2006 May;42(8):1031-9. doi: 10.1016/j.ejca.2006.01.026. Epub 2006 Apr 17.
7
Measuring response in solid tumors: comparison of RECIST and WHO response criteria.实体瘤反应的测量:RECIST与WHO反应标准的比较。
Jpn J Clin Oncol. 2003 Oct;33(10):533-7. doi: 10.1093/jjco/hyg093.
8
CT tumor measurement for therapeutic response assessment: comparison of unidimensional, bidimensional, and volumetric techniques initial observations.用于治疗反应评估的CT肿瘤测量:一维、二维和容积技术的比较——初步观察
Radiology. 2002 Nov;225(2):416-9. doi: 10.1148/radiol.2252011604.
9
Comparison of unidimensional and bidimensional measurements in metastatic non-small cell lung cancer.转移性非小细胞肺癌中一维与二维测量的比较
Br J Cancer. 2002 Jul 15;87(2):158-60. doi: 10.1038/sj.bjc.6600449.
10
Tissue mimicking materials for a multi-imaging modality prostate phantom.用于多模态成像前列腺体模的组织模拟材料。
Med Phys. 2001 Apr;28(4):688-700. doi: 10.1118/1.1354998.

使用组织模拟材料构建临床前多模态体模用于肿瘤大小测量的质量保证。

Construction of a preclinical multimodality phantom using tissue-mimicking materials for quality assurance in tumor size measurement.

作者信息

Lee Yongsook C, Fullerton Gary D, Goins Beth A

机构信息

Department of Radiation Oncology, University of Kansas School of Medicine.

出版信息

J Vis Exp. 2013 Jul 29(77):50403. doi: 10.3791/50403.

DOI:10.3791/50403
PMID:23928940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3846463/
Abstract

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).

摘要

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)。