Evidence map›Paper›PMID 42088645›Full record

ArticleAdvances in neural information processing systems2025

STARC-9: A Large-scale Dataset for Multi-Class Tissue Classification for CRC Histopathology.

Barathi Subramanian, Rathinaraja Jeyaraj, Mitchell Nevin Peterson, Terry Guo, Nigam Shah, Curtis Langlotz, Andrew Y Ng, Jeanne Shen

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Article in Advances in neural information processing systems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Barathi SubramanianDepartment of Pathology, Stanford University, USA.
Rathinaraja JeyarajDepartment of Pathology, Stanford University, USA.
Mitchell Nevin PetersonDepartment of Electrical Engineering, Stanford University, USA.
Terry GuoDepartment of Pathology, Stanford University, USA.
Nigam ShahDepartment of Medicine, Stanford University, USA.
Curtis LanglotzDepartment of Radiology, Stanford University, USA.
Andrew Y NgDepartment of Computer Science, Stanford University, USA.
Jeanne ShenDepartment of Pathology, Stanford University, USA.

Funding

Multi-modal machine learning to guide adjuvant therapy in surgically resectable colorectal cancerR01CA270437 · NCI · STANFORD UNIVERSITY · PI Jeanne Shen · 2023 to 2026
$2.5M
NCI NIH HHS R01 CA270437
6 · The paper itself

Abstract

Multi-class tissue-type classification of colorectal cancer (CRC) histopathologic images is a significant step in the development of downstream machine learning models for diagnosis and treatment planning. However, publicly available CRC datasets used to build tissue classifiers often suffer from insufficient morphologic diversity, class imbalance, and low-quality image tiles, limiting downstream model performance and generalizability. To address this research gap, we introduce STARC-9 (STAnford coloRectal Cancer), a large-scale dataset for multi-class tissue classification. STARC-9 comprises 630,000 histopathologic image tiles uniformly sampled across nine clinically relevant tissue classes (each represented by 70,000 tiles), systematically extracted from hematoxylin & eosin-stained whole-slide images (WSI) from 200 CRC patients at the Stanford University School of Medicine. To construct STARC-9, we propose a novel framework, DeepCluster++, consisting of two primary steps to ensure diversity within each tissue class, followed by pathologist verification. First, an encoder from an autoencoder trained specifically on histopathologic images is used to extract feature vectors from all tiles within a given input WSI. Next, K-means clustering groups morphologically similar tiles, followed by an equal-frequency binning method to sample diverse patterns within each tissue class. Finally, the selected tiles are verified by expert gastrointestinal pathologists to ensure classification accuracy. This semi-automated approach significantly reduces the manual effort required for dataset curation while producing high-quality training examples. To validate the utility of STARC-9, we benchmarked baseline convolutional neural networks, transformers, and pathology-specific foundation models on downstream multi-class CRC tissue classification and segmentation tasks when trained on STARC-9 versus publicly available datasets, demonstrating superior generalizability of models trained on STARC-9. Although we demonstrate the utility of DeepCluster++ on CRC as a pilot use-case, it is a flexible framework that can be used for constructing high-quality datasets from large WSI repositories across a wide range of cancer and non-cancer applications. https://huggingface.co/datasets/Path2AI/STARC-9/tree/main https://github.com/Path2AI/STARC-9/.

Identifiers

PMID42088645
PMCPMC13138521

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.