# Benchmarking Pathology Feature Extractors for Whole Slide Image Classification

Source: [Benchmarking Pathology Feature Extractors for Whole Slide Image Classification](<https://www.sota2.com/research/paper/68fa73c11e209131cea5e47b>)

Collection index: [llms.txt](<https://www.sota2.com/research/llms.txt>)

Data updated: 2025-10-26T02:56:12.281Z

Authors: Georg W\\"olflein, Dyke Ferber, Asier R. Meneghetti, Omar S. M. El Nahhas, Daniel Truhn, Zunamys I. Carrero, David J. Harrison, Ognjen Arandjelovi\\'c, Jakob Nikolas Kather (2 and 3 and 5) \_\_INSTITUTION\_9\_\_ University of St Andrews, St Andrews, United Kingdom, (2) Else Kr\\"oner Fresenius Center for Digital Health, Medical Faculty Carl Gustav Carus, TUD Dresden University of Technology, Dresden, Germany, (3) Department of Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany, (4) University Hospital Aachen, Germany, (5) Department of Medicine I, University Hospital Dresden, Dresden, Germany)

Published: 2023-11-20T13:58:26.000Z

## Abstract

Weakly supervised whole slide image classification is a key task in computational pathology, which involves predicting a slide-level label from a set of image patches constituting the slide. Constructing models to solve this task involves multiple design choices, often made without robust empirical or conclusive theoretical justification. To address this, we conduct a comprehensive benchmarking of feature extractors to answer three critical questions: 1) Is stain normalisation still a necessary preprocessing step? 2) Which feature extractors are best for downstream slide-level classification? 3) How does magnification affect downstream performance? Our study constitutes the most comprehensive evaluation of publicly available pathology feature extractors to date, involving more than 10,000 training runs across 14 feature extractors, 9 tasks, 5 datasets, 3 downstream architectures, 2 levels of magnification, and various preprocessing setups. Our findings challenge existing assumptions: 1) We observe empirically, and by analysing the latent space, that skipping stain normalisation and image augmentations does not degrade performance, while significantly reducing memory and computational demands. 2) We develop a novel evaluation metric to compare relative downstream performance, and show that the choice of feature extractor is the most consequential factor for downstream performance. 3) We find that lower-magnification slides are sufficient for accurate slide-level classification. Contrary to previous patch-level benchmarking studies, our approach emphasises clinical relevance by focusing on slide-level biomarker prediction tasks in a weakly supervised setting with external validation cohorts. Our findings stand to streamline digital pathology workflows by minimising preprocessing needs and informing the selection of feature extractors.

## Recorded benchmark results

A research result applies to its stated dataset, split, metric and evaluation configuration. Compare like-for-like settings, preserve the metric's unit and direction, and distinguish paper-reported results from independent reproduction. The best result recorded here is not a claim of exhaustive, current global coverage.

## Original sources and implementation

[Original paper](<https://arxiv.org/abs/2311.11772>)

[PDF](<https://arxiv.org/pdf/2311.11772.pdf>)
