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Lightweight deep models based on domain adaptation and network pruning for breast cancer HER2 scoring: IHC vs. H&E histopathological images

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Abstract

Human epidermal growth factor receptor 2 (HER2)-positive breast cancer is an aggressive cancer type that requires special diagnosis and treatment methods. Immunohistochemistry (IHC) staining effectively highlights relevant morphological structures within histopathological images yet can be expensive in terms of both labor and required laboratory equipment. Hematoxylin and eosin (H&E) images are more readily available and less expensive than IHC images as they are routinely performed for all patient samples. Lightweight models are well-suited for deployment on resource-constrained devices such as mobile phones and embedded systems, making them ideal for real-time diagnosis in rural regions and developing countries. In this study, IHC images are compared to H&E images for automatic HER2 scoring using lightweight deep models that incorporate several advanced techniques including network pruning, domain adaptation, and attention mechanisms. Two lightweight models are presented: PrunEff4 and ATHER2. PrunEff4 is a subset of EfficientNetV2B0 pruned to reduce the network parameters by ~80%. ATHER2 is a customized lightweight network that employs different sized convolutional filters along with a convolutional block attention module (CBAM). For PrunEff4 and ATHER2, transfer learning (pretraining on ImageNet) and domain-specific pretraining were employed, respectively. Different datasets were utilized in the development and final testing phases in order to effectively evaluate their generalization capability. In all experiments, both networks resulted in accuracies ranging from 97% to 100% for binary classifications and from 95.5% to 98.5% for multiclass classifications regardless of whether IHC or H&E images were utilized. Network pruning significantly reduced the network parameters whilst maintaining reliable performance. Domain-specific pretraining significantly enhanced performance, particularly in complex classification tasks such as HER2 scoring using H&E images and multiclass classifications. Both IHC and H&E stained images were suitable for deep learning-based HER2 scoring, given that the deep networks are efficiently trained for the specified task.
Original languageEnglish
Article numbere0332362
Pages (from-to)1-30
Number of pages30
JournalPLoS One
Volume20
Issue number9
Early online date15 Sept 2025
DOIs
Publication statusPublished online - 15 Sept 2025

Bibliographical note

Publisher Copyright:
© 2025 Abdel-Hamid et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability Statement

The author(s) received no specific funding for this work.

Funding

All images used in this study were taken from the following publicly available datasets: (1) BCI (BCImmunohistochemical Image Generation) dataset: https://bci.grand-challenge.org/ (2) Warwick dataset: https://warwick.ac.uk/fac/cross_fac/tia/data/her2contest/ (3) BreakHis (BC Histopathological) dataset https://web.inf.ufpr.br/vri/databases/breast-cancer-histopathological-database-breakhis/. The source code for presented lightweight modes is publicly available at: https://github.com/LamiaaSy/her2-lite/.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Humans
  • Breast Neoplasms/pathology
  • Receptor, ErbB-2/metabolism
  • Female
  • Immunohistochemistry/methods
  • Deep Learning
  • Image Processing, Computer-Assisted/methods
  • Hematoxylin
  • Eosine Yellowish-(YS)
  • Immunohistochemistry
  • Breast Neoplasms
  • Receptor, erbB-2
  • Image Processing, Computer-Assisted
  • Receptor, ErbB-2 - metabolism
  • Breast Neoplasms - pathology - metabolism - diagnosis
  • Image Processing, Computer-Assisted - methods
  • Immunohistochemistry - methods

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