Incorporation of diffusion-weighted magnetic resonance imaging data into a simple mathematical model of tumor growth

被引:32
作者
Atuegwu, N. C. [1 ,4 ]
Colvin, D. C. [1 ,4 ]
Loveless, M. E. [1 ,2 ]
Xu, L. [3 ]
Gore, J. C. [1 ,2 ,4 ,5 ,6 ]
Yankeelov, T. E. [1 ,2 ,4 ,5 ,7 ]
机构
[1] Vanderbilt Univ Nashville, Inst Imaging Sci, Nashville, TN 37240 USA
[2] Vanderbilt Univ Nashville, Dept Biomed Engn, Nashville, TN USA
[3] Vanderbilt Univ Nashville, Dept Biostat, Nashville, TN USA
[4] Vanderbilt Univ Nashville, Dept Radiol & Radiol Sci, Nashville, TN USA
[5] Vanderbilt Univ Nashville, Dept Phys & Astron, Nashville, TN USA
[6] Vanderbilt Univ Nashville, Dept Mol Physiol & Biophys, Nashville, TN USA
[7] Vanderbilt Univ Nashville, Dept Canc Biol, Nashville, TN USA
基金
美国国家卫生研究院;
关键词
BRAIN-TUMORS; FRACTION; MRI;
D O I
10.1088/0031-9155/57/1/225
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We build on previous work to show how serial diffusion-weighted MRI (DW-MRI) data can be used to estimate proliferation rates in a rat model of brain cancer. Thirteen rats were inoculated intracranially with 9L tumor cells; eight rats were treated with the chemotherapeutic drug 1,3-bis(2-chloroethyl)-1-nitrosourea and five rats were untreated controls. All animals underwent DW-MRI immediately before, one day and three days after treatment. Values of the apparent diffusion coefficient (ADC) were calculated from the DW-MRI data and then used to estimate the number of cells in each voxel and also for whole tumor regions of interest. The data from the first two imaging time points were then used to estimate the proliferation rate of each tumor. The proliferation rates were used to predict the number of tumor cells at day three, and this was correlated with the corresponding experimental data. The voxel-by-voxel analysis yielded Pearson's correlation coefficients ranging from -0.06 to 0.65, whereas the region of interest analysis provided Pearson's and concordance correlation coefficients of 0.88 and 0.80, respectively. Additionally, the ratio of positive to negative proliferation values was used to separate the treated and control animals (p < 0.05) at an earlier point than the mean ADC values. These results further illustrate how quantitative measurements of tumor state obtained non-invasively by imaging can be incorporated into mathematical models that predict tumor growth.
引用
收藏
页码:225 / 240
页数:16
相关论文
共 26 条
[1]   Effects of cell volume fraction changes on apparent diffusion in human cells [J].
Anderson, AW ;
Xie, J ;
Pizzonia, J ;
Bronen, RA ;
Spencer, DD ;
Gore, JC .
MAGNETIC RESONANCE IMAGING, 2000, 18 (06) :689-695
[2]   The integration of quantitative multi-modality imaging data into mathematical models of tumors [J].
Atuegwu, Nkiruka C. ;
Gore, John C. ;
Yankeelov, Thomas E. .
PHYSICS IN MEDICINE AND BIOLOGY, 2010, 55 (09) :2429-2449
[3]  
Byrne HM, 2003, MATH COMP BIOL SER, P75
[4]  
Chenevert TL, 1997, CLIN CANCER RES, V3, P1457
[5]   Earlier detection of tumor treatment response using magnetic resonance diffusion imaging with oscillating gradients [J].
Colvin, Daniel C. ;
Loveless, Mary E. ;
Does, Mark D. ;
Yue, Zou ;
Yankeelov, Thomas E. ;
Gore, John C. .
MAGNETIC RESONANCE IMAGING, 2011, 29 (03) :315-323
[6]  
Galons Jean-Philippe, 1999, Neoplasia (New York), V1, P113, DOI 10.1038/sj.neo.7900009
[7]   Therapeutic efficacy of DTI-015 using diffusion magnetic resonance imaging as an early surrogate marker [J].
Hall, DE ;
Moffat, BA ;
Stojanovska, J ;
Johnson, TD ;
Li, ZL ;
Hamstra, DA ;
Rehemtulla, A ;
Chenevert, TL ;
Carter, J ;
Pietronigro, D ;
Ross, BD .
CLINICAL CANCER RESEARCH, 2004, 10 (23) :7852-7859
[8]  
Hayashida Y, 2006, AM J NEURORADIOL, V27, P1419
[9]   An image-driven parameter estimation problem for a reaction-diffusion glioma growth model with mass effects [J].
Hogea, Cosmina ;
Davatzikos, Christos ;
Biros, George .
JOURNAL OF MATHEMATICAL BIOLOGY, 2008, 56 (06) :793-825
[10]  
Hogea C, 2007, LECT NOTES COMPUT SC, V4791, P642