Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Transl Oncol. 2009 Dec;2(4):211-5. doi: 10.1593/tlo.09241.
This article describes methods and issues that are specific to the assessment of change in tumor characteristics as measured using quantitative magnetic resonance (MR) techniques and how this relates to the establishment of quantitative MR imaging (MRI) biomarkers of patient response to therapy. The initial focus is on the various sources of bias and variance in the measurement of microvascular parameters and diffusion parameters as such parameters are being used relatively commonly as secondary or exploratory end points in current phase 1/2 clinical trails of conventional and targeted therapies. Several ongoing initiatives that seek to identify the magnitude of some of the sources of measurement variations are then discussed. Finally, resources being made available through the National Cancer Institute Reference Image Database to Evaluate Response (RIDER) project that might be of use in investigations of quantitative MRI biomarker change analysis are described. These resources include 1) data from phantom-based assessment of system response, including short-term (1 hour) and moderate-term (1 week) contrast response and relaxation time measurement, 2) data obtained from repeated dynamic contrast agent-enhanced MRI studies in intracranial tumors, and 3) data obtained from repeated diffusion MRI studies in both breast and brain. A concluding section briefly discusses issues that must be addressed to allow the transition of MR-based imaging biomarker measures from their current role as secondary/exploratory end points in clinical trials to primary/surrogate markers of response and, ultimately, in clinical application.
本文描述了使用定量磁共振(MR)技术评估肿瘤特征变化时特定的方法和问题,以及这与建立治疗反应的定量磁共振成像(MRI)生物标志物之间的关系。最初的重点是测量微血管参数和扩散参数时各种来源的偏差和方差,因为这些参数作为次要或探索性终点,在目前常规和靶向治疗的 1 期/2 期临床试验中相对较为常用。然后讨论了几个正在进行的旨在确定一些测量变化源的幅度的倡议。最后,描述了国家癌症研究所参考图像数据库以评估反应(RIDER)项目提供的资源,这些资源可能有助于定量 MRI 生物标志物变化分析的研究。这些资源包括 1)基于体模的系统响应评估数据,包括短期(1 小时)和中期(1 周)对比响应和弛豫时间测量,2)颅内肿瘤重复动态对比增强 MRI 研究获得的数据,以及 3)在乳腺和大脑中重复扩散 MRI 研究获得的数据。最后一节简要讨论了为了允许基于磁共振的成像生物标志物测量从目前临床试验中的次要/探索性终点过渡到反应的主要/替代标志物,并最终过渡到临床应用,必须解决的问题。