Chaddad Ahmad, Niazi Tamim, Probst Stephan, Bladou Franck, Anidjar Maurice, Bahoric Boris
Division of Radiation Oncology, McGill University, Montreal, QC, Canada.
Department of Automated Production Engineering, ETS, Montreal, QC, Canada.
Front Oncol. 2018 Dec 18;8:630. doi: 10.3389/fonc.2018.00630. eCollection 2018.
Use of quantitative imaging features and encoding the intra-tumoral heterogeneity from multi-parametric magnetic resonance imaging (mpMRI) for the prediction of Gleason score is gaining attention as a non-invasive biomarker for prostate cancer (PCa). This study tested the hypothesis that radiomic features, extracted from mpMRI, could predict the Gleason score pattern of patients with PCa. This analysis included T2-weighted (T2-WI) and apparent diffusion coefficient (ADC, computed from diffusion-weighted imaging) scans of 99 PCa patients from The Cancer Imaging Archive (TCIA). A total of 41 radiomic features were calculated from a local tumor sub-volume (i.e., regions of interest) that is determined by a centroid coordinate of PCa volume, grouped based on their Gleason score patterns. Kruskal-Wallis and Spearman's rank correlation tests were used to identify features related to Gleason score groups. Random forest (RF) classifier model was used to predict Gleason score groups and identify the most important signature among the 41 radiomic features. Gleason score groups could be discriminated based on zone size percentage, large zone size emphasis and zone size non-uniformity values ( < 0.05). These features also showed a significant correlation between radiomic features and Gleason score groups with a correlation value of -0.35, 0.32, 0.42 for the large zone size emphasis, zone size non-uniformity and zone size percentage, respectively (corrected < 0.05). RF classifier model achieved an average of the area under the curves of the receiver operating characteristic (ROC) of 83.40, 72.71, and 77.35% to predict Gleason score groups (G1) = 6; 6 < (G2) < (3 + 4) and (G3) ≥ 4 + 3, respectively. Our results suggest that the radiomic features can be used as a non-invasive biomarker to predict the Gleason score of the PCa patients.
利用定量成像特征并通过多参数磁共振成像(mpMRI)编码肿瘤内异质性来预测 Gleason 评分,作为前列腺癌(PCa)的一种非侵入性生物标志物正受到关注。本研究检验了这样一个假设:从 mpMRI 中提取的放射组学特征能够预测 PCa 患者的 Gleason 评分模式。该分析纳入了来自癌症影像存档(TCIA)的 99 例 PCa 患者的 T2 加权(T2-WI)和表观扩散系数(ADC,由扩散加权成像计算得出)扫描图像。从由 PCa 体积的质心坐标确定的局部肿瘤子体积(即感兴趣区域)中计算出总共 41 个放射组学特征,并根据 Gleason 评分模式进行分组。采用 Kruskal-Wallis 检验和 Spearman 秩相关检验来识别与 Gleason 评分组相关的特征。使用随机森林(RF)分类器模型来预测 Gleason 评分组,并在 41 个放射组学特征中识别出最重要的特征。基于区域大小百分比、大区域大小权重和区域大小不均匀性值(<0.05)能够区分 Gleason 评分组。这些特征还显示出放射组学特征与 Gleason 评分组之间存在显著相关性,大区域大小权重、区域大小不均匀性和区域大小百分比的相关值分别为 -0.35、0.32、0.42(校正后 <0.05)。RF 分类器模型预测 Gleason 评分组(G1)=6、6<(G2)<(3 + 4)和(G3)≥4 + 3 时,受试者操作特征(ROC)曲线下面积的平均值分别为 83.40%、72.71%和 77.35%。我们的结果表明,放射组学特征可作为一种非侵入性生物标志物来预测 PCa 患者的 Gleason 评分。