Temporal Sampling Requirements for Reference Region Modeling of DCE-MRI Data in Human Breast Cancer

被引:31
作者
Planey, Catherine R. [2 ]
Welch, E. Brian [3 ]
Xu, Lei [4 ]
Chakravarthy, A. Bapsi [5 ]
Gatenby, J. Christopher [6 ]
Freehardt, Darla [7 ]
Mayer, Ingrid [7 ]
Meszeoly, Ingrid [8 ]
Kelley, Mark [8 ]
Means-Powell, Julie [8 ]
Gore, John C. [6 ,9 ,10 ,11 ]
Yankeelov, Thomas E. [1 ,9 ,10 ,12 ]
机构
[1] Vanderbilt Univ, Med Ctr, Inst Imaging Sci, Nashville, TN 37232 USA
[2] Yale Univ, Dept Biomed Engn, New Haven, CT USA
[3] Philips Healthcare, MR Clin Sci, Cleveland, OH USA
[4] Vanderbilt Univ, Dept Biostat, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Dept Radiat Oncol, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Dept Radiol & Radiol Sci, Nashville, TN 37232 USA
[7] Vanderbilt Univ, Dept Oncol, Nashville, TN 37232 USA
[8] Vanderbilt Univ, Dept Surg Oncol, Nashville, TN 37232 USA
[9] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37232 USA
[10] Vanderbilt Univ, Dept Phys & Astron, Nashville, TN 37232 USA
[11] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[12] Vanderbilt Univ, Dept Canc Biol, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
DCE-MRI; breast cancer; temporal sampling; pharmacokinetics; CONTRAST-ENHANCED MRI; ARTERIAL INPUT FUNCTION; TRANSCYTOLEMMAL WATER EXCHANGE; RESONANCE-IMAGING MEASUREMENTS; HIGH FAMILIAL RISK; NEOADJUVANT CHEMOTHERAPY; PHARMACOKINETIC ANALYSIS; REFERENCE TISSUES; TRACER KINETICS; BOLUS INJECTION;
D O I
10.1002/jmri.21812
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: To assess the temporal sampling requirements needed for quantitative analysis of dynamic contrast-enhanced MRI (DCE-MRI) data with a reference region (RR) model in human breast cancer. Materials and Methods: Simulations were used to study errors in pharmacokinetic parameters (K-trans and upsilon(e)) estimated by the RR model using six DCE-MRI acquisitions over a range of pharmacokinetic parameter values, arterial input functions, and temporal samplings. DCE-MRI data were acquired on 12 breast cancer patients and parameters were estimated using the native resolution data (16.4 seconds) and compared to downsampled 32.8-second and 65.6-second data. Results: Simulations show that, in the majority of parameter combinations, the RR model results in an error less than 20% in the extracted parameters with temporal sampling as poor as 35.6 seconds. The experimental results show a high correlation between K-trans and upsilon(e) estimates from data acquired at 16.4-second temporal resolution compared to the downsampled 32.8-second data: the slope of the regression line was 1.025 (95% confidence interval [CI]: 1.021, 1.029). Pearson's correlation r = 0.943 (95% CI: 0.940, 0.945) for K-trans and 1.023 (95% CI: 1.021. 1.025), r = 0.979 (95% CI: 0.978, 0.980) for upsilon(e). For the 64-second temporal resolution data the results were: 0.890 (95% CI: 0.894, 0.905), r = 0.8645, (95% CI: 0.858, 0.871) for K-trans, and 1.041 (95% Cl: 1.039, 1.043), r = 0.970 (95% Cl: 0.968, 0.971) for upsilon(e). Conclusion: RR analysis allows for a significant reduction in temporal sampling requirements and this lends itself to analyze DCE-MRI data acquired in practical situations.
引用
收藏
页码:121 / 134
页数:14
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