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arXiv 2408.02859eess.IVcs.AIcs.CV

用于病理学切片表征学习的多重染色预训练

Multistain Pretraining for Slide Representation Learning in Pathology

Harvard Medical School(哈佛医学院);Mass General Brigham(麻省总医院布里格姆医疗系统)

Guillaume Jaume, Anurag Vaidya, Andrew Zhang, Andrew H. Song, Richard J. Chen, Sharifa Sahai, Dandan Mo, Emilio Madrigal, Long Phi Le, Faisal Mahmood

AI总结:

本文提出Madeleine多模态预训练框架,利用不同标志物染色的WSI作为视图并进行全局—局部跨染色对齐,在21项病理下游任务上验证了切片表征的泛化能力。

摘要:

开发能够学习H&E千兆像素全切片图像(WSI)通用且可迁移表征的自监督学习(SSL)模型,在计算病理学中正变得越来越有价值。这些模型有望推进少样本分类、切片检索和患者分层等关键任务。现有的切片表征学习方法通常通过对齐同一切片的两种不同增强(或视图),将小图像(例如224×224图块)上的SSL原则扩展到整张切片。然而,所得表征仍受限于这些视图有限的临床和生物学多样性。相反,我们假设采用多种标志物染色的切片(例如免疫组织化学)可以作为不同视图,形成丰富的、与任务无关的训练信号。为此,我们提出了Madeleine,这是一种用于切片表征学习的多模态预训练策略。Madeleine采用双重全局—局部跨染色对齐目标,在乳腺癌样本大队列(5种染色共N=4,211张WSI)和肾移植样本队列(4种染色共N=12,070张WSI)上进行训练。我们在多种下游评估中证明了Madeleine所学切片表征的质量,评估涵盖形态学和分子分类到预后预测,共包括来自多个医疗中心的7,299张WSI上的21项任务。代码可在https://github.com/mahmoodlab/MADELEINE获取。

英文摘要:

Developing self-supervised learning (SSL) models that can learn universal and transferable representations of H&E gigapixel whole-slide images (WSIs) is becoming increasingly valuable in computational pathology. These models hold the potential to advance critical tasks such as few-shot classification, slide retrieval, and patient stratification. Existing approaches for slide representation learning extend the principles of SSL from small images (e.g., 224 x 224 patches) to entire slides, usually by aligning two different augmentations (or views) of the slide. Yet the resulting representation remains constrained by the limited clinical and biological diversity of the views. Instead, we postulate that slides stained with multiple markers, such as immunohistochemistry, can be used as different views to form a rich task-agnostic training signal. To this end, we introduce Madeleine, a multimodal pretraining strategy for slide representation learning. Madeleine is trained with a dual global-local cross-stain alignment objective on large cohorts of breast cancer samples (N=4,211 WSIs across five stains) and kidney transplant samples (N=12,070 WSIs across four stains). We demonstrate the quality of slide representations learned by Madeleine on various downstream evaluations, ranging from morphological and molecular classification to prognostic prediction, comprising 21 tasks using 7,299 WSIs from multiple medical centers. Code is available at https://github.com/mahmoodlab/MADELEINE.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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