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通过 DW-MRI 和 DCE-MRI 数据对肿瘤生长的 logistic 模型进行参数化,以预测新辅助化疗期间乳腺癌细胞数量的治疗反应和变化。

Parameterizing the Logistic Model of Tumor Growth by DW-MRI and DCE-MRI Data to Predict Treatment Response and Changes in Breast Cancer Cellularity during Neoadjuvant Chemotherapy.

机构信息

Institute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN ; Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, TN.

出版信息

Transl Oncol. 2013 Jun 1;6(3):256-64. doi: 10.1593/tlo.13130. Print 2013 Jun.

Abstract

Diffusion-weighted and dynamic contrast-enhanced magnetic resonance imaging (MRI) data of 28 patients were obtained pretreatment, after one cycle, and after completion of all cycles of neoadjuvant chemotherapy (NAC). For each patient at each time point, the tumor cell number was estimated using the apparent diffusion coefficient and the extravascular extracellular (v e) and plasma volume (v p) fractions. The proliferation/death rate was obtained using the number of tumor cells from the first two time points in conjunction with the logistic model of tumor growth, which was then used to predict tumor cellularity at the conclusion of NAC. The Pearson correlation coefficient between the predicted and the experimental number of tumor cells measured at the end of NAC was 0.81 (P = .0043). The proliferation rate estimated after the first cycle of therapy was able to separate patients who went on to achieve pathologic complete response from those who did not (P = .021) with a sensitivity and specificity of 82.4% and 72.7%, respectively. These data provide preliminary results indicating that incorporating readily available quantitative MRI data into a simple model of tumor growth can lead to potentially clinically relevant information for predicting an individual patient's response to NAC.

摘要

对 28 例患者的弥散加权和动态对比增强磁共振成像(MRI)数据进行了预处理、一个周期后和所有新辅助化疗(NAC)周期完成后的采集。对于每个患者的每个时间点,使用表观扩散系数以及血管外细胞外(v e)和血浆体积(v p)分数来估算肿瘤细胞数量。使用前两个时间点的肿瘤细胞数量并结合肿瘤生长的逻辑模型来获得增殖/死亡率,然后将其用于预测 NAC 结束时的肿瘤细胞密度。在 NAC 结束时测量的预测和实验肿瘤细胞数之间的 Pearson 相关系数为 0.81(P =.0043)。在治疗的第一个周期后估计的增殖率能够将继续实现病理完全缓解的患者与未实现的患者区分开来(P =.021),其敏感性和特异性分别为 82.4%和 72.7%。这些数据提供了初步结果,表明将易于获得的定量 MRI 数据纳入肿瘤生长的简单模型中,可以为预测个体患者对 NAC 的反应提供潜在的临床相关信息。

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