Evidence map›Paper›PMID 39386823›Full record

ArticleHeliyon2024

CAE-ResVGG FusionNet: A Feature Extraction Framework Integrating Convolutional Autoencoders and Transfer Learning for Immature White Blood Cells in Acute Myeloid Leukemia.

Tusneem Elhassan, Ahmed Hamza Osman, Mohd Shafry Mohd Rahim, Siti Zaiton Mohd Hashim, Abdulalem Ali, Esmaeil Elhassan, Yusra Elkamali, Mahmoud Aljurf

Abstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Observational
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

8 authors.

Tusneem ElhassanCancer Center of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh 11564, Saudi Arabia.
Ahmed Hamza OsmanDepartment of Information Systems, Faculty of Computing and Information Technology, King Abdulaziz University Rabigh, Saudi Arabia.
Mohd Shafry Mohd RahimSchool of Computing, Universiti Teknologi Malaysia, Johor Bahru 81310, Johor, Malaysia.
Siti Zaiton Mohd HashimSchool of Computing, Universiti Teknologi Malaysia, Johor Bahru 81310, Johor, Malaysia.
Abdulalem AliInstitute of Computer Science and Digital Innovation, UCSI University, Federal Territory of Kuala Lumpur.
Esmaeil ElhassanSchool of Computing, Universiti Teknologi Malaysia, Johor Bahru 81310, Johor, Malaysia.
Yusra ElkamaliFaculty of mathematical science, university of Khartoum, Sudan.
Mahmoud AljurfDept of Hematology, Stem Cell Transplantation and Cellular Therapy, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a highly aggressive cancer form that affects myeloid cells, leading to the excessive growth of immature white blood cells (WBCs) in both bone marrow and peripheral blood. Timely AML detection is crucial for effective treatment and patient well-being. Currently, AML diagnosis relies on the manual recognition of immature WBCs through peripheral blood smear analysis, which is time-consuming, prone to errors, and subject to inter-observers' variation. This study aimed to develop a computer-aided diagnostic framework for AML, called "CAE-ResVGG FusionNet", that precisely identifies and classifies immature WBCs into their respective subtypes. The proposed framework leverages an integrated approach, by combining a convolutional autoencoder (CAE) with finely tuned adaptations of the VGG19 and ResNet50 architectures to extract features from CAE-derived embeddings. The process begins with a binary classification model distinguishing between mature and immature WBCs followed by a multiclassifier further classifying immature cells into four subtypes: myeloblasts, monoblasts, erythroblasts, and promyelocytes. The CAE-ResVGG FusionNet workflow comprises four primary stages, including data preprocessing, feature extraction, classification, and validation. The preprocessing phase involves applying data augmentation methods using geometric transformations and synthetic image generation using the CAE to address imbalance in the WBC distribution. Feature extraction involves image embedding and transfer learning, where CAE-derived image representations are used by a custom integrated model of VGG19 and ResNet50 pretrained models. The classification phase employs a weighted ensemble approach that leverages VGG19 and ResNet50, where the optimal weighting parameters are selected using a grid search. The model performance was assessed during the validation phase using the overall accuracy, precision, and sensitivity, while the area under the receiver characteristic curve (AUC) was used to evaluate the model's discriminatory capability. The proposed framework exhibited notable results, achieving an average accuracy of 99.9%, sensitivity of 91.7%, and precision of 98.8%. The model demonstrated exceptional discriminatory ability, as evidenced by an AUC of 99.6%. Significantly, the proposed system outperformed previous methods, indicating its superior diagnostic ability.

Indexed as

Acute myeloid leukemiaAutoencoderblood smear microscopic imagesCancerComputer-aided diagnosis modelimage classificationImmature white blood cellsResNetVGG19

Identifiers

PMID39386823
PMCPMC11462284

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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.