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Non-invasive Transcriptomic Classification of de novo Glioblastoma Patients through Multivariate Quantitative Analysis of Baseline Preoperative Multimodal Magnetic Resonance Imaging

机译:De Novo胶质母细胞瘤患者的非侵入性转录组分类通过多元术前术前多峰磁共振成像的多元定量分析

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Glioblastoma, the most common primary malignant brain tumor, is genetically diverse and classified into four transcriptomic subtypes, i.e., classical, mesenchymal, proneural, neural. We sought a noninvasive robust quantitative imaging phenomic (QIP) signature associated with this transcriptomic classification of glioblastoma patients, derived from clinically-acquired imaging protocols and without the need for advanced genetic testing. This QIP signature was discovered and evaluated in a retrospective cohort of 112 pathology-proven de novo glioblastoma patients for whom basic preoperative multi-parametric MRI (mpMRI) data (TI, Tl-Gd, T2, T2-FLAIR) were available, and compared with the tumor subtype as obtained through an RNA isoform-based classifier. Comprehensive and diverse QIP features capturing intensity distributions, volume, morphology, statistics, tumors' anatomical location, and texture for each tumor sub-region, were multivariately integrated via support vector machines to construct our QIP signature. The performance/generalizability of the model was evaluated using 5-fold cross-validation. The overall accuracy of the proposed method was estimated equal to 71% for identifying the transcriptomic tumor subtype; 82.14% [AUC:0.82], 75.89% [AUC:0.78], 75.89% [AUC:0.81], and 88.39% [AUC:0.84] for predicting proneural, neural, mesenchymal and classical subtypes, respectively. The obtained QIP signature revealed a macroscopic biological insight of the complex tumor subtypes, including more pronounced presence of tissue with higher water content in neural subtype, larger enhancement component of the tumor in mesenchymal subtype, and overall smaller tumors in classical subtype. Our results indicate that quantitative analysis of imaging features extracted from clinically-acquired mpMRI yields prompt non-invasive biomarkers of the molecular profile of glioblastoma patients, important in influencing surgical decision-making, treatment planning, and assessment of inoperab
机译:胶质母细胞瘤,最常见的原发性恶性脑肿瘤,在遗传上是不同的,并分为四种亚型转录,即,古典,间充质,原神经,神经。我们寻求与胶质母细胞瘤患者的这种转录分类,从临床上获得的成像协议,也不需要先进的基因检测得出相关的非侵入性的强大的定量成像phenomic(QIP)的签名。这QIP签名被发现,在112病理证实的从头胶质母细胞瘤患者的回顾性队列研究对他们来说基本术前多参数MRI(mpMRI)数据(TI,铊钆,T2,T2-FLAIR)是可利用的评估,并进行比较与肿瘤亚型通过一个基于同种型RNA分类器获得的。全面多样QIP功能捕获的强度分布,体积,形态,统计,肿瘤的解剖位置,和纹理为每个肿瘤子区域,通过支持向量机被集成multivariately构建我们QIP签名。该模型的性能/概评价使用5倍交叉验证。所提出的方法的整体精度估计等于71%用于识别转录肿瘤亚型; 82.14%[AUC:0.82],75.89%[AUC:0.78],75.89%[AUC:0.81],和88.39%[AUC:0.84],用于分别预测原神经,神经,间质和古典亚型。将所得到的签名QIP揭示了复杂的肿瘤亚型的宏观生物洞察,包括与在神经亚型较高的水含量的组织的更明显的存在下,在间充质亚型肿瘤的更大的增强部件,并且在经典亚型整体更小的肿瘤。我们的研究结果表明,成像的定量分析,从临床上获得的mpMRI提取的特征产生胶质母细胞瘤患者的分子谱的提示非侵入性的生物标志物的影响手术的决策,治疗计划,重要的是,和inoperab的评估

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