融合病理报告、病理图像和生物通路,提升癌症生存预测准确率
PS3: A Multimodal Transformer Integrating Pathology Reports with Histology Images and Biological Pathways for Cancer Survival Prediction
- 用原型提取法将三类数据转为统一表示,解决模态差异问题
- 在TCGA六个数据集上优于现有方法,显著提升生存预测性能
- 适合临床辅助决策研究者,尤其关注多模态融合的医学AI团队
当前计算肿瘤学中的多模态融合主要整合超大尺寸病理全切片图像(WSIs)与基因组或转录组数据,已证明可改善生存预测。我们假设引入病理报告可进一步提升预后表现。病理报告作为临床工作流的关键部分,以简洁文本总结组织学发现,并融入专家判断与临床背景,具有易获取的互补价值。然而,由于其与高维图像间存在显著异质性——每张WSI含数十亿像素,而报告文本长度不一,导致模态不平衡。为此,我们提出基于原型的方法生成均衡表示,并通过基于Transformer的融合模型(命名为PS3)实现生存预测。具体包括:(1) 从病理报告中提取诊断原型,利用自注意力机制识别关键信息并标准化文本表示;(2) 构建组织学原型,紧凑表达WSI中的关键形态模式;(3) 建立生物通路原型,编码转录组表达,精准捕捉细胞功能。PS3模型处理三类原型生成的多模态令牌,建模模态内与跨模态交互。在来自TCGA的六个数据集上,相较于临床、单模态及多模态基线,该模型表现更优。代码已公开于:https://github.com/manahilr/PS3。
原文摘要 · Abstract (English)
Current multimodal fusion approaches in computational oncology primarily focus on integrating multi-gigapixel histology whole slide images (WSIs) with genomic or transcriptomic data, demonstrating improved survival prediction. We hypothesize that incorporating pathology reports can further enhance prognostic performance. Pathology reports, as essential components of clinical workflows, offer readily available complementary information by summarizing histopathological findings and integrating expert interpretations and clinical context. However, fusing these modalities poses challenges due to their heterogeneous nature. WSIs are high-dimensional, each containing several billion pixels, whereas pathology reports consist of concise text summaries of varying lengths, leading to potential modality imbalance. To address this, we propose a prototype-based approach to generate balanced representations, which are then integrated using a Transformer-based fusion model for survival prediction that we term PS3 (Predicting Survival from Three Modalities). Specifically, we present: (1) Diagnostic prototypes from pathology reports, leveraging self-attention to extract diagnostically relevant sections and standardize text representation; (2) Histological prototypes to compactly represent key morphological patterns in WSIs; and (3) Biological pathway prototypes to encode transcriptomic expressions, accurately capturing cellular functions. PS3, the three-modal transformer model, processes the resulting prototype-based multimodal tokens and models intra-modal and cross-modal interactions across pathology reports, WSIs and transcriptomic data. The proposed model outperforms state-of-the-art methods when evaluated against clinical, unimodal and multimodal baselines on six datasets from The Cancer Genome Atlas (TCGA). The code is available at: https://github.com/manahilr/PS3.
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