Evidence map›Paper›PMID 41776189›Full record

ArticleScientific reports2026

Hybrid EfficientNet B4 and SVM framework for rapid and accurate bone cancer diagnosis from X-rays.

Nashaat M Hussain Hassan, Ahmed S Bayoumy, Mohamed Hassan M Mahmoud

Abstract read
In one paragraph

Article in Scientific reports, 2026. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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.

Nashaat M Hussain HassanElectronics and Communication Engineering Dept, Fayoum University, Fayoum, 63514, Egypt. nmh01@fayoum.edu.eg.
Ahmed S BayoumyPhysics and Engineering Mathematics Department, Faculty of Engineering, Kafrelsheikh University, Kafrelsheikh, 33516, Egypt.
Mohamed Hassan M MahmoudGiza Institute for Higher Education and Technology, Giza, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The early and correct diagnosis of bone cancer is important for treating both primary and metastatic conditions effectively. Traditional imaging techniques, like CT, MRI, and X-ray scans, depend exclusively on manual review, which is time-consuming and prone to human errors. Recently, ML and DL have enabled automated diagnostic systems that are more accurate, reliable, and efficient. Still, many of the existing approaches using DL suffer from high computational complexity, overfitting, and limited availability of robust datasets. This work proposes a novel diagnostic model for bone cancer, called OsteoCancerNet, which combines EfficientNetB4 for feature extraction with a support vector machine using the RBF kernel for classification. EfficientNetB4 captures efficiently both quantitative and qualitative features from X-ray images, and the SVM ensures robust binary classification. Extensive experiments using a large dataset with 29,952 X-ray images demonstrate that OsteoCancerNet provides 98% precision, 97.47% recall, 98% accuracy, and a 98% F1-score, thus outperforming traditional machine learning, deep learning, and transfer learning methods. Of note, the model maintains fast inference times of 41 milliseconds per image, making it suitable for real-time clinical applications. By combining deep learning feature extraction with traditional machine learning classification, OsteoCancerNet provides an efficient, accurate, and practical approach for the early detection of bone cancer. This approach has the potential to aid radiologists in timely diagnosis, decrease workload, and improve treatment outcomes, thus underlining the advantages of integrating DL and ML techniques within medical imaging. Keywords: OsteoCancerNet; computer-assisted diagnosis; bone cancer diagnosis; EfficientNet B4 model; SVM model; X-ray image analysis.

Indexed as

Bone NeoplasmsSupport Vector MachineAlgorithmsClassification AlgorithmsConvolutional Neural NetworksHumansRadiography

Identifiers

PMID41776189
PMCPMC12960689

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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.