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Radiopathomics: Integration of radiographic and histologic characteristics for prognostication in glioblastoma

接收机工作特性 人工智能 直方图 随机森林 胶质母细胞瘤 流体衰减反转恢复 支持向量机 模式识别(心理学) 磁共振成像 医学 计算机科学 核医学 放射科 机器学习 癌症研究 图像(数学)
作者
Saima Rathore,Muhammad Aksam Iftikhar,Metin N. Gürcan,Zissimos P. Mourelatos
出处
期刊:Cornell University - arXiv [Cornell University]
标识
DOI:10.48550/arxiv.1909.07581
摘要

Both radiographic (Rad) imaging, such as multi-parametric magnetic resonance imaging, and digital pathology (Path) images captured from tissue samples are currently acquired as standard clinical practice for glioblastoma tumors. Both these data streams have been separately used for diagnosis and treatment planning, despite the fact that they provide complementary information. In this research work, we aimed to assess the potential of both Rad and Path images in combination and comparison. An extensive set of engineered features was extracted from delineated tumor regions in Rad images, comprising T1, T1-Gd, T2, T2-FLAIR, and 100 random patches extracted from Path images. Specifically, the features comprised descriptors of intensity, histogram, and texture, mainly quantified via gray-level-co-occurrence matrix and gray-level-run-length matrices. Features extracted from images of 107 glioblastoma patients, downloaded from The Cancer Imaging Archive, were run through support vector machine for classification using leave-one-out cross-validation mechanism, and through support vector regression for prediction of continuous survival outcome. The Pearson correlation coefficient was estimated to be 0.75, 0.74, and 0.78 for Rad, Path and RadPath data. The area-under the receiver operating characteristic curve was estimated to be 0.74, 0.76 and 0.80 for Rad, Path and RadPath data, when patients were discretized into long- and short-survival groups based on average survival cutoff. Our results support the notion that synergistically using Rad and Path images may lead to better prognosis at the initial presentation of the disease, thereby facilitating the targeted enrollment of patients into clinical trials.

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