Navigating Through Whole Slide Images With Hierarchy, Multi-Object, and Multi-Scale Data

Manuel Tran;Sophia Wagner;Wilko Weichert;Christian Matek;Melanie Boxberg;Tingying Peng
{"title":"Navigating Through Whole Slide Images With Hierarchy, Multi-Object, and Multi-Scale Data","authors":"Manuel Tran;Sophia Wagner;Wilko Weichert;Christian Matek;Melanie Boxberg;Tingying Peng","doi":"10.1109/TMI.2025.3532728","DOIUrl":null,"url":null,"abstract":"Building deep learning models that can rapidly segment whole slide images (WSIs) using only a handful of training samples remains an open challenge in computational pathology. The difficulty lies in the histological images themselves: many morphological structures within a slide are closely related and very similar in appearance, making it difficult to distinguish between them. However, a skilled pathologist can quickly identify the relevant phenotypes. Through years of training, they have learned to organize visual features into a hierarchical taxonomy (e.g., identifying carcinoma versus healthy tissue, or distinguishing regions within a tumor as cancer cells, the microenvironment, …). Thus, each region is associated with multiple labels representing different tissue types. Pathologists typically deal with this by analyzing the specimen at multiple scales and comparing visual features between different magnifications. Inspired by this multi-scale diagnostic workflow, we introduce the Navigator, a vision model that navigates through WSIs like a domain expert: it searches for the region of interest at a low scale, zooms in gradually, and localizes ever finer microanatomical classes. As a result, the Navigator can detect coarse-grained patterns at lower resolution and fine-grained features at higher resolution. In addition, to deal with sparsely annotated samples, we train the Navigator with a novel semi-supervised framework called S5CL v2. The proposed model improves the F1 score by up to 8% on various datasets including our challenging new TCGA-COAD-30CLS and Erlangen cohorts.","PeriodicalId":94033,"journal":{"name":"IEEE transactions on medical imaging","volume":"44 5","pages":"2002-2015"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE transactions on medical imaging","FirstCategoryId":"1085","ListUrlMain":"https://ieeexplore.ieee.org/document/10849962/","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Building deep learning models that can rapidly segment whole slide images (WSIs) using only a handful of training samples remains an open challenge in computational pathology. The difficulty lies in the histological images themselves: many morphological structures within a slide are closely related and very similar in appearance, making it difficult to distinguish between them. However, a skilled pathologist can quickly identify the relevant phenotypes. Through years of training, they have learned to organize visual features into a hierarchical taxonomy (e.g., identifying carcinoma versus healthy tissue, or distinguishing regions within a tumor as cancer cells, the microenvironment, …). Thus, each region is associated with multiple labels representing different tissue types. Pathologists typically deal with this by analyzing the specimen at multiple scales and comparing visual features between different magnifications. Inspired by this multi-scale diagnostic workflow, we introduce the Navigator, a vision model that navigates through WSIs like a domain expert: it searches for the region of interest at a low scale, zooms in gradually, and localizes ever finer microanatomical classes. As a result, the Navigator can detect coarse-grained patterns at lower resolution and fine-grained features at higher resolution. In addition, to deal with sparsely annotated samples, we train the Navigator with a novel semi-supervised framework called S5CL v2. The proposed model improves the F1 score by up to 8% on various datasets including our challenging new TCGA-COAD-30CLS and Erlangen cohorts.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过层次结构、多对象和多尺度数据导航整个幻灯片图像
构建能够仅使用少量训练样本快速分割整个幻灯片图像(wsi)的深度学习模型仍然是计算病理学中的一个开放挑战。难点在于组织学图像本身:幻灯片中的许多形态结构密切相关,在外观上非常相似,因此很难区分它们。然而,熟练的病理学家可以快速识别相关表型。通过多年的训练,他们已经学会了将视觉特征组织成一个层次分类法(例如,识别癌组织和健康组织,或区分肿瘤内的区域为癌细胞,微环境等)。因此,每个区域都与代表不同组织类型的多个标签相关联。病理学家通常通过在多个尺度上分析标本并比较不同放大倍数下的视觉特征来处理这个问题。受这种多尺度诊断工作流程的启发,我们引入了Navigator,这是一种像领域专家一样在wsi中导航的视觉模型:它以低尺度搜索感兴趣的区域,逐渐放大,并定位更精细的微观解剖类。因此,Navigator可以在较低分辨率下检测粗粒度模式,在较高分辨率下检测细粒度特征。此外,为了处理稀疏注释的样本,我们使用一种称为S5CL v2的新型半监督框架来训练Navigator。所提出的模型在各种数据集上的F1分数提高了8%,包括我们具有挑战性的新TCGA-COAD-30CLS和Erlangen队列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Decouple, Reorganize, and Fuse: A Multimodal Framework for Cancer Survival Prediction. MARVEL: Motion-Aware Reconstruction Via Embedded Learning of Motion Prior for Time-Resolved Cardiac CT. QuPaS: SAM-based Semi-supervised Histopathological Image Segmentation with Quantum Force Field Finetuning and Adversarial Estimation. Dynamic Registration-Based Photoacoustic Endoscopic Temperature Imaging for Precision Interventional Thermal Therapy and Monitoring. Scan-invariant Mamba with Differentiated Sequence Contrastive Learning in Computational Pathology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1