Evidence map›Paper›PMID 40953092›Full record

ArticlePloS one2025

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

Lamiaa Abdel-Hamid, Pratheepan Yogarajah, Safy Hosny Ahmed Tealab

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Lamiaa Abdel-HamidElectronics and Communication Department, Faculty of Engineering, Misr International University, Cairo, Egypt.ORCID https://orcid.org/0000-0002-4066-6021
Pratheepan YogarajahSchool of Computing, Engineering and Intelligent Systems, University of Ulster, Londonderry, United Kingdom.
Safy Hosny Ahmed TealabPathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Breast NeoplasmsDeep LearningErb-b2 Receptor Tyrosine KinasesImmunohistochemistryEosine Yellowish-(YS)FemaleHematoxylinHumansImage Processing, Computer-AssistedEosine Yellowish-(YS)ERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHematoxylin

Identifiers

PMID40953092
PMCPMC12435681

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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.