ArticleScientific reports2025
Optimized federated learning framework with RegNetZ and Swin-Transformer for multimodal pancreatic cancer detection1.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- DGFI-Net: dual-branch guided feature interaction network for brain tumor segmentation.Frontiers in physiology · 2026Article
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pancreatic cancer is among the most lethal malignancies, marked by aggressive progression, late diagnosis, and limited screening methods, resulting in a five-year survival rate of less than 10%. Early-stage tumors are especially challenging to detect with standard CT and MRI imaging, leading to treatment delays and poor outcomes. While deep learning offers promise, centralized training in healthcare raises serious privacy and data-sharing concerns. This study introduces a federated learning framework that integrates RegNetZ and the Swin-Transformer for automated detection, subtype classification, and prognosis prediction from multimodal inputs, including CT, MRI, histology, genomic, and clinical records. The Swin-Transformer models long-range dependencies, whereas the lightweight RegNetZ backbone ensures efficient local feature extraction. A Hybrid Aquila-Grey Wolf Optimizer (HA-GWO) is incorporated to balance exploration and exploitation during hyperparameter tuning, providing faster convergence and reduced computational cost compared to conventional search strategies. The proposed framework, evaluated across 5-7 simulated client institutions, achieves 99.2% accuracy, 98.9% sensitivity, 99.0% precision, and 99.4% AUC, outperforming both CNN-only and transformer-only baselines. It further minimizes false positives and false negatives, improving both subtype classification (adenocarcinoma, neuroendocrine, cystic neoplasms) and prognosis risk prediction (high vs. low risk). Hyperparameter sensitivity analysis identifies a learning rate of 0.003 with a batch size of 64 as optimal. By enabling decentralized model training without raw data exchange, the system enhances diagnostic accuracy while preserving privacy, offering a practical solution for real-time pancreatic cancer detection in federated healthcare environments. The framework is scalable across medical institutions and supports precision oncology by enabling early and reliable diagnosis at low computational cost.
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Registered trials
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.