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Magnetic resonance image features identify glioblastoma phenotypic subtypes with distinct molecular pathway activities

机译:磁共振图像特征识别具有不同分子途径活性的胶质母细胞瘤表型亚型

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摘要

Glioblastoma (GBM) is the most common and highly lethal primary malignant brain tumor in adults. There is a dire need for easily accessible, noninvasive biomarkers that can delineate underlying molecular activities and predict response to therapy. To this end, we sought to identify subtypes of GBM, differentiated solely by quantitative MR imaging features, that could be used for better management of GBM patients. Quantitative image features capturing the shape, texture, and edge sharpness of each lesion were extracted from MR images of 121 patients with de novo, solitary, unilateral GBM. Three distinct phenotypic “clusters” emerged in the development cohort using consensus clustering with 10,000 iterations on these image features. These three clusters—pre-multifocal, spherical, and rim-enhancing, names reflecting their image features—were validated in an independent cohort consisting of 144 multi-institution patients with similar tumor characteristics from The Cancer Genome Atlas (TCGA). Each cluster mapped to a unique set of molecular signaling pathways using pathway activity estimates derived from analysis of TCGA tumor copy number and gene expression data with the PARADIGM algorithm. Distinct pathways, such as c-Kit and FOXA, were enriched in each cluster, indicating differential molecular activities as determined by image features. Each cluster also demonstrated differential probabilities of survival, indicating prognostic importance. Our imaging method offers a noninvasive approach to stratify GBM patients and also provides unique sets of molecular signatures to inform targeted therapy and personalized treatment of GBM.
机译:胶质母细胞瘤(GBM)是成人中最常见,最致命的原发性恶性脑肿瘤。迫切需要一种易于获得的,非侵入性的生物标志物,该标志物可以描述潜在的分子活性并预测对治疗的反应。为此,我们寻求鉴定仅通过定量MR成像特征加以区分的GBM亚型,这些亚型可用于更好地管理GBM患者。从121例初发,单发,单侧GBM患者的MR图像中提取定量图像特征,以捕获每个病变的形状,纹理和边缘清晰度。通过使用共识聚类对这些图像特征进行10,000次迭代,在开发队列中出现了三个不同的表型“簇”。这三个群-多焦点前,球形和边缘增强,反映其图像特征的名称-在由144位来自癌症基因组图谱(TCGA)具有相似肿瘤特征的多机构患者组成的独立队列中得到验证。使用通过PARADIGM算法对TCGA肿瘤拷贝数和基因表达数据进行分析得出的途径活性估计,将每个簇映射到一组独特的分子信号途径。不同的途径(例如c-Kit和FOXA)在每个簇中富集,表明通过图像特征确定的不同分子活性。每个聚类还显示出不同的生存概率,表明预后的重要性。我们的成像方法提供了一种非侵入性方法来对GBM患者进行分层,并且还提供了独特的分子标记集,可为GBM的靶向治疗和个性化治疗提供依据。

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