Foundation Models for Histopathology—Fanfare or Flair

Saghir Alfasly PhD , Peyman Nejat MD , Sobhan Hemati PhD , Jibran Khan , Isaiah Lahr , Areej Alsaafin PhD , Abubakr Shafique PhD , Nneka Comfere MD , Dennis Murphree PhD , Chady Meroueh MD , Saba Yasir MBBS , Aaron Mangold MD , Lisa Boardman MD , Vijay H. Shah MD , Joaquin J. Garcia MD , H.R. Tizhoosh PhD
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Abstract

Objective

To assess the performance of the current foundation models in histopathology.

Patients and Methods

The assessment involves a comprehensive evaluation of some foundation models, such as the CLIP derivatives, namely PLIP and BiomedCLIP, which were fine-tuned on data scraped from the internet. The comparison is performed against simpler and nonfoundational histology models that are trained on well-curated data, eg, the cancer genome atlas. All models are evaluated on 8 datasets, 4 of which are internal histology datasets collected and curated at Mayo Clinic, and 4 well-known public datasets: PANDA, BRACS, CAMELYON16, and DigestPath. Evaluation metrics include accuracy and macro-averaged F1 score, using a majority vote among top-k (eg, MV@5) at the whole slide image/patch levels. Moreover, all models are evaluated in classification settings. This detailed analysis allows for a deep understanding of each model’s performance across various datasets.

Results

In various evaluation tasks, domain-specific (and nonfoundational) models like DinoSSLPath and KimiaNet outperform general-purpose foundation models. The DinoSSLPath excels in whole slide image-level retrieval for internal colorectal cancer and liver datasets with MV@5 macro-averaged F1 scores of 63% and 74%, respectively. The KimiaNet leads in breast and skin cancer tasks with respective Top-1 and MV@5 scores of 56% and 70%, respectively and scores 75% on the public CAMELYON16 dataset. Similar trends are observed in patch-level metrics, highlighting the advantage of using specialized datasets like the cancer genome atlas for histopathological analysis.

Conclusion

To enable effective vision-language foundation models in biomedicine, high-quality, multi-modal medical datasets are essential. These datasets serve as the substrate for training models capable of translating research into clinical practice. Of importance, the alignment (correspondence) between textual and visual data—often diagnostic—is critical and requires validation by domain experts. Thus, advancing foundation models in this field necessitates collaborative efforts in data curation and validation.

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组织病理学基础模型--狂热还是炫耀
患者和方法评估包括对一些基础模型的综合评估,如 CLIP 衍生模型,即 PLIP 和 BiomedCLIP,这些模型是根据从互联网上搜刮的数据进行微调的。比较的对象是在癌症基因组图谱等经过精心整理的数据基础上训练的更简单的非基础组织学模型。所有模型都在 8 个数据集上进行了评估,其中 4 个是梅奥诊所收集和整理的内部组织学数据集,另外 4 个是著名的公共数据集:PANDA、BRACS、CAMELYON16 和 DigestPath。评估指标包括准确率和宏观平均 F1 分数,在整张幻灯片图像/斑块级别上采用前 k(如 MV@5)中的多数票。此外,所有模型都在分类设置中进行了评估。结果在各种评估任务中,DinoSSLPath 和 KimiaNet 等特定领域(非基础)模型的表现优于通用基础模型。DinoSSLPath 在内部结直肠癌和肝脏数据集的整张幻灯片图像级检索中表现出色,MV@5 宏观平均 F1 分数分别为 63% 和 74%。KimiaNet 在乳腺癌和皮肤癌任务中遥遥领先,Top-1 和 MV@5 分数分别为 56% 和 70%,在公共 CAMELYON16 数据集上的分数为 75%。在斑块级指标中也观察到了类似的趋势,这凸显了使用癌症基因组图谱等专业数据集进行组织病理学分析的优势。这些数据集是训练能够将研究成果转化为临床实践的模型的基础。重要的是,文本数据和视觉数据(通常是诊断数据)之间的对齐(对应)至关重要,需要领域专家的验证。因此,要推进该领域的基础模型,就必须在数据整理和验证方面开展合作。
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来源期刊
Mayo Clinic Proceedings. Digital health
Mayo Clinic Proceedings. Digital health Medicine and Dentistry (General), Health Informatics, Public Health and Health Policy
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