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Real-Time Quantitative Assessment of Accuracy and Precision of Blood Volume Derived from DCE-MRI in Individual Patients During a Clinical Trial

机译:在临床试验中对个体患者DCE-MRI得出的血容量的准确性和准确性进行实时定量评估

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摘要

Accuracy and precision of quantitative imaging (QI) metrics should be assessed in real time in each patient during a clinical trial to support QI-based decision-making. We developed a framework for real-time quantitative assessment of QI metrics and evaluated accuracy and precision of dynamic contrast-enhanced (DCE)-magnetic resonance imaging (MRI)–derived blood volume (BV) in a clinical trial for head and neck cancers. Patients underwent DCE-MRI before and after 2 weeks of radiation therapy (2wkRT). A mean as a reference value and a repeatability coefficient (RC) of BV values established from n patients in cerebellum volumes of interest (VOIs), which were normal and affected little by therapy, served as accuracy and precision measurements. The BV maps of a new patient were called accurate and precise if the values in cerebellum VOIs and the difference between the 2 scans agreed with the respective mean and RC with 95% confidence. The new data could be used to update reference values. Otherwise, the data were flagged for further evaluation before use in the trial. BV maps from 62 patients enrolled on the trial were evaluated. Mean BV values were 2.21 (±0.14) mL/100 g pre-RT and 2.22 (±0.17) mL/100 g at 2wkRT; relative RC was 15.9%. The BV maps from 3 patients were identified to be inaccurate and imprecise before use in the clinical trial. Our framework of real-time quantitative assessment of QI metrics during a clinical trial can be translated to different QI metrics and organ-sites for supporting QI-based decision-making that warrants success of a clinical trial.
机译:在临床试验期间,应实时评估每位患者的定量成像(QI)指标的准确性和准确性,以支持基于QI的决策。我们开发了一种用于QI指标实时定量评估的框架,并在一项针对头颈癌的临床试验中评估了动态对比增强(DCE)-磁共振成像(MRI)衍生的血容量(BV)的准确性和精确度。患者在放疗(2wkRT)2周前后接受DCE-MRI检查。从正常和受治疗影响很小的感兴趣的小脑体积(VOIs)中的n名患者建立的平均值作为参考值和BV值的可重复性系数(RC),作为准确性和精密度测量。如果小脑VOI值和两次扫描之间的差值分别与各自的平均值和RC符合95%的置信度,则将新患者的BV图称为准确和精确。新数据可用于更新参考值。否则,将数据标记为用于试验之前的进一步评估。评估了来自该试验的62名患者的BV图。在2wkRT时,平均BV值在RT前为2.21(±0.14)mL / 100 g,在2wkRT下为2.22(±0.17)mL / 100 g;相对RC为15.9%。在用于临床试验之前,已确定3名患者的BV图不准确且不准确。我们在临床试验期间对QI指标进行实时定量评估的框架可以转换为不同的QI指标和器官部位,以支持基于QI的决策,从而确保临床试验的成功。

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