Institute of Imaging Science, Vanderbilt University Nashville, TN, USA.
Phys Med Biol. 2012 Jan 7;57(1):225-40. doi: 10.1088/0031-9155/57/1/225.
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.
我们在前人的工作基础上进一步研究,展示了如何利用连续弥散加权磁共振成像(DW-MRI)数据来估计脑癌大鼠模型中的增殖率。13 只大鼠颅内接种 9L 肿瘤细胞;8 只大鼠接受化疗药物 1,3-双(2-氯乙基)-1-亚硝基脲治疗,5 只大鼠为未治疗对照组。所有动物在治疗前、治疗后 1 天和 3 天均进行 DW-MRI 检查。从 DW-MRI 数据中计算表观扩散系数(ADC)值,然后用于估计每个体素和整个肿瘤感兴趣区的细胞数量。然后,使用前两个成像时间点的数据来估计每个肿瘤的增殖率。将增殖率用于预测第 3 天的肿瘤细胞数量,并将其与相应的实验数据进行相关分析。体素分析得到的 Pearson 相关系数范围为-0.06 至 0.65,而感兴趣区分析的 Pearson 相关系数和一致性相关系数分别为 0.88 和 0.80。此外,增殖值的阳性与阴性比值可用于在 ADC 值平均值之前将治疗组和对照组动物区分开来(p<0.05)。这些结果进一步说明如何将通过成像无创获得的肿瘤状态的定量测量值纳入预测肿瘤生长的数学模型中。