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Overall survival time prediction for high-grade glioma patients based on large-scale brain functional networks

Authors
Liu, LuyanZhang, HanWu, JinsongYu, ZhengdaChen, XiaoboRekik, IslemWang, QianLu, JunfengShen, Dinggang
Issue Date
10월-2019
Publisher
SPRINGER
Keywords
Survival; Prognosis; Glioma; Functional connectivity; Brain network; Connectomics; Machine learning
Citation
BRAIN IMAGING AND BEHAVIOR, v.13, no.5, pp.1333 - 1351
Indexed
SCIE
SCOPUS
Journal Title
BRAIN IMAGING AND BEHAVIOR
Volume
13
Number
5
Start Page
1333
End Page
1351
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/62693
DOI
10.1007/s11682-018-9949-2
ISSN
1931-7557
Abstract
High-grade glioma (HGG) is a lethal cancer with poor outcome. Accurate preoperative overall survival (OS) time prediction for HGG patients is crucial for treatment planning. Traditional presurgical and noninvasive OS prediction studies have used radiomics features at the local lesion area based on the magnetic resonance images (MRI). However, the highly complex lesion MRI appearance may have large individual variability, which could impede accurate individualized OS prediction. In this paper, we propose a novel concept, namely brain connectomics-based OS prediction. It is based on presurgical resting-state functional MRI (rs-fMRI) and the non-local, large-scale brain functional networks where the global and systemic prognostic features rather than the local lesion appearance are used to predict OS. We propose that the connectomics features could capture tumor-induced network-level alterations that are associated with prognosis. We construct both low-order (by means of sparse representation with regional rs-fMRI signals) and high-order functional connectivity (FC) networks (characterizing more complex multi-regional relationship by synchronized dynamics FC time courses). Then, we conduct a graph-theoretic analysis on both networks for a jointly, machine-learning-based individualized OS prediction. Based on a preliminary dataset (N = 34 with bad OS, mean OS, similar to 400 days; N = 34 with good OS, mean OS, similar to 1030 days), we achieve a promising OS prediction accuracy (86.8%) on separating the individuals with bad OS from those with good OS. However, if using only conventionally derived descriptive features (e.g., age and tumor characteristics), the accuracy is low (63.2%). Our study highlights the importance of the rs-fMRI and brain functional connectomics for treatment planning.
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