PO.BCS02.04 · 生物信息与计算

通过在潜在空间中由Kaniadakis向量嵌入提取的多模态放射组学表型,对术后GBM患者进行基于深度学习的生存预测

Deep learning-based survival prediction of post-operative GBM patients via multimodal radiomic phenotypes drawn from Kaniadakis vector embedding in latent space

海报缩略图:通过在潜在空间中由Kaniadakis向量嵌入提取的多模态放射组学表型,对术后GBM患者进行基于深度学习的生存预测
编号 2791 展板 22 时间 4/20 02:00–05:00 区域 Section 4 主讲 Bardia Rodd, PhD
分会场 Radiomics and AI in Medical Imaging
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作者与单位 Authors & Affiliations

Roy Nasr, Bardia Rodd

SUNY Upstate Medical University, Syracuse, NY

摘要 Abstract

中文摘要
目的:本研究旨在利用多模态影像生物标志物和AI引导的个性化精准生存预测,改善术后胶质母细胞瘤(GBM)患者的结局。 方法:分析了来自宾夕法尼亚大学的450例初发GBM病例队列,每例均包含四个标准多模态MRI序列(T1、T2、FLAIR、T1-Gadolinium)。我们对每个模态提取了354个放射组学生物标志物(Pyradiomics),并使用基于密度的Isomap(PR-Isomap)将这些高维特征降至一个稳定的11维潜在空间,其最优维度由我们专门为此类投影所开发的间隙统计量(gap statistic)确定。随后对这些潜在生物标志物进行归一化、跨模态融合,并通过Kappa(Kaniadakis)向量嵌入投影到风险敏感的特征空间。所得的多模态特征输入一个基于深度学习的生存模型,采用对数风险比,通过基于Cox比例风险模型负对数似然的生存损失函数进行优化,以进行患者结局预测。 结果:最终的生存预测模型通过多个机器学习分类器的共识(10折交叉验证)在二分类中取得了71.7%的准确率,C-index为0.5196,表明仅使用影像嵌入即具有适度但具统计学意义的预测能力。为评估预后区分度,按风险评分四分位数对Kaplan-Meier生存曲线进行分层。确立了明确的阈值:第一四分位数(Q1)风险评分为-0.36,第三四分位数(Q3)评分为-0.29。中位风险评分-0.33将队列分为225例高风险患者和225例低风险患者。所得的分层Kaplan-Meier曲线显示出这些风险组之间的清晰分离,明确证实了MRI衍生嵌入区分患者生存轨迹的能力。 结论:将深度学习与多模态MRI嵌入相整合,为GBM预后评估提供了一种强大而客观的方法。所得的定量风险评分成功区分了高风险和低风险患者的生存轨迹。这种由多模态影像生物标志物驱动的方法为术后GBM患者提供了个性化风险信息,并通过为个性化辅助治疗的选择提供依据,支持精准神经肿瘤学。
查看英文原文 English abstract
Purpose: The aim of this study was to use multimodal imaging biomarkers and AI-guided personalized precision survival prediction in improving outcomes for patients with post-operative glioblastoma (GBM). Method: A cohort of 450 de novo GBM cases from the University of Pennsylvania, each featuring the four standard multimodal MRI sequences (T1, T2, FLAIR, T1-Gadolinium), was analyzed. We extracted 354 radiomic biomarkers per modality (Pyradiomics) and reduced these high-dimensional features to a stable 11-dimensional latent space using Density-Based Isomap (PR-Isomap), with the optimal dimension determined by a gap statistic, which we developed specifically for such projection. These latent biomarkers were then normalized, fused across modalities, and projected into a risk-sensitive feature space via Kappa (Kaniadakis) Vector Embedding. The resulting multimodal features fed into a deep learning-based survival model using the log-hazard ratio, optimized via a survival loss function based on the negative log-likelihood of the Cox proportional hazards model for patient outcome prediction. Results: The final survival-prediction model achieved a 71.7% accuracy in binary classification via a consensus of multiple machine learning classifiers with 10-fold cross-validation and a C-index of 0.5196, indicating a modest but statistically meaningful predictive capability using the imaging embeddings alone. To assess prognostic separation, a Kaplan-Meier survivorship curve was stratified by hazard-score quartiles. Distinct thresholds were established: the first quartile Q1) hazard score was -0.36 and the third quartile (Q3) score was -0.29. The median hazard score of -0.33 separated the cohort into 225 high-hazard patients and 225 low-hazard patients. The resulting stratified Kaplan-Meier curves demonstrated clear separation between these risk groups, definitively confirming the capacity of the MRI-derived embeddings to differentiate patient survival trajectories. Conclusion: The integration of deep learning with multimodal MRI embeddings offers a powerful, objective methodology for GBM prognostication. The resulting quantitative hazard scores successfully differentiate high- and low-risk patient survival trajectories. This multimodal imaging biomarker-driven approach provides personalized risk information for post-operative GBM patients, and supporting precision neuro-oncology by informing the selection of personalized adjuvant therapies.
利益披露 Disclosure
R. Nasr, None.. B. Rodd, None.

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