Evidence map›Paper›PMID 42804475›Full record

ArticlePLOS digital health2026

Independent evaluation of machine learning and deep learning models for breast cancer detection.

Deepthi, Ashalatha Nayak, Rani Oomman Panicker

Abstract read
In one paragraph

Article in PLOS digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

DeepthiManipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India.ORCID https://orcid.org/0009-0006-6526-6848
Ashalatha NayakManipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India.ORCID https://orcid.org/0000-0001-7888-6516
Rani Oomman PanickerManipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is one of the leading causes of cancer-related mortality worldwide, and despite advances in clinical diagnosis, challenges such as inconclusive imaging results and inter-observer variability highlight the need for complementary computational approaches to support early and accurate detection. In this study, we provide an overview of several machine learning (ML) and deep learning (DL) algorithms used for breast cancer detection with structured clinical data and imaging data. We applied ML models to structured clinical data which included Wisconsin Breast Cancer Dataset, CSAW-CC dataset and SEER database using Random Forest, Decision Tree, Logistic Regression, Gradient Boosting, and Bayesian classifier models. DL models, specifically Convolutional Neural Networks (CNN), ResNet50, VGG16, and DenseNet, were utilized in mammography, histopathology, and ultrasound datasets. The experimental results show that the DL models outperformed ML models in image classification tasks, obtaining accuracy rates of 97.88% for histopathological images and 92.00% for ultrasound data. However, ensemble-based and probabilistic ML models achieved strong performance on structured clinical data, with predictive accuracy of up to 98%. All performance metrics are reported with 95% confidence intervals.Model calibration was assessed using the Expected Calibration Error (ECE) and reliability diagrams. Logistic Regression, Gradient Boosting, and Random Forest produced the best-calibrated probability estimates among the structured-data classifiers, while the transfer-learning-based deep convolutional architectures were well calibrated on the histopathology imaging datasets. Calibration was comparatively weaker for Decision Tree and Naive Bayes among the structured-data classifiers, as well as for the from-scratch CNN baseline and some deep learning models evaluated on the smaller BUSI dataset. The results indicate that model performance is significantly influenced by data modality and that artificial intelligence may serve as a valuable computational tool to support clinical breast cancer diagnosis workflow. Further prospective validation using clinical data across diverse patient populations will be essential to confirm the robustness, interpretability, and generalizability of these findings.

Identifiers

PMID42804475
PMCPMC13618913

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.