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剖析并指导病理学基础模型

英文原题:Dissecting and directing pathology foundation models.

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Dissecting and directing pathology foundation models.

PubMed 2026/06/16(内容时间) bioRxiv

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中文摘要

基础模型(FMs)是数字病理学的核心,将组织学图像编码为稠密嵌入,以促进诊断分类、分子改变预测和临床结局建模。然而,这些嵌入的不透明性使基于FM的系统成为“黑箱”,限制了其在临床转化中的可信度以及在科学发现中的实用性。

在此,我们介绍PICASSO(通过稀疏字典学习构建的病理图像概念图谱),一个使病理FM可解释且可控的框架。PICASSO使用稀疏自编码器将FM嵌入分解为人类可解释的视觉概念。它在涵盖32种癌症类型的超过1.2亿个组织斑块上进行训练,产生了首个泛癌组织形态学概念图谱。

我们证明,PICASSO通过揭示学习表示中可解释的结构并支持概念层面的干预,实现了FM嵌入的多样化下游应用。它通过揭示驱动预测的形态学特征,实现了对临床模型行为的审计。除了透明性和验证之外,PICASSO还能够发现新的生物学见解;例如,它识别出鞋钉样上皮形态是肺腺癌中EGFR突变的一个此前未被认识的生物标志物。通过将PICASSO衍生的概念与空间转录组学相关联,我们揭示了形态学模式与基因表达程序之间的关联。

此外,PICASSO允许抑制与技术伪影相关的概念,从而减少模型对虚假信号的依赖。最后,PICASSO 能够对学习到的概念进行受控操作,以生成反事实嵌入用于探索性治疗分析,例如调节TIL(肿瘤浸润淋巴细胞)密度以评估其对预测生存结局的影响。

总之,PICASSO 提供了一个原则性框架,将病理基础模型转化为机制洞察与发现的平台。

展开英文摘要原文

Foundation models (FMs) are central to digital pathology, encoding histology images into dense embeddings for facilitating diagnostic classification, molecular alteration prediction, and clinical outcome modeling.

However, the opacity of these embeddings renders FM-based systems "black boxes," limiting their trustworthiness for clinical translation and utility for scientific discovery.

Here, we introduce PICASSO ( P athology I mage C oncept A tlas built via S par S e dicti O nary learning), a framework that makes pathology FMs interpretable and controllable. PICASSO decomposes FM embeddings into human-interpretable visual concepts using a sparse autoencoder. It is trained on more than 120 million tissue patches across 32 cancer types, producing the first pan-cancer atlas of histomorphological concepts.

We demonstrate that PICASSO enables diverse downstream applications of FM embeddings by exposing interpretable structure within learned representations and supporting concept-level intervention. It enables auditing of clinical model behavior by revealing the morphological features driving predictions.

Beyond transparency and validation, PICASSO enables the discovery of new biological insights; for example, it identified hobnailing epithelial morphology as a previously unrecognized biomarker of EGFR mutations in lung adenocarcinoma. By linking PICASSO-derived concepts with spatial transcriptomics, we uncover associations between morphological patterns and gene expression programs.

Furthermore, PICASSO allows suppression of concepts associated with technical artifacts, thereby reducing model reliance on spurious signals.

Finally, PICASSO enables controlled manipulation of learned concepts to generate counterfactual embeddings for exploratory therapeutic analysis, such as modulating tumour-infiltrating lymphocyte density to assess impacts on predict survival outcomes.

Together, PICASSO provides a principled framework for transforming pathology FMs into platforms for mechanistic insight and discovery.

论文信息

作者
Kim C、Kaczmarzyk J、Savant D、Zhao Z、Koo PK、Lee SI
单位
Paul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA, USA.United States
文献类型
预印本
期刊
bioRxiv : the preprint server for biology2026 Jun 16
原文标识
PubMed 42367854 · DOI 10.64898/2026.06.12.731496