Evidence map›Paper›PMID 42052410›Full record

ArticleDigital health

Classification of hematologic malignancies from whole-slide bone marrow aspirates using a two-stage deep convolutional neural network pipeline.

Hung-Ruei Chen, Yao-Chung Liu, Chiu-Mei Yeh, Cheng-Kuan Lin, Tzu-Ya Chien, Ying-Chung Hong, Chia-Jen Liu, Kun-Hsing Yu

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

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8 authors.

Hung-Ruei ChenSchool of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-7292-397X
Yao-Chung LiuSchool of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Chiu-Mei YehDivision of Transfusion Medicine, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Cheng-Kuan LinDepartment of Computer Science, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
Tzu-Ya ChienIndustry Academia Innovation School, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
Ying-Chung HongSchool of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Chia-Jen LiuDivision of Transfusion Medicine, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0001-7945-9292
Kun-Hsing YuDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Morphologic information from bone marrow (BM) examinations remains critical for diagnosing leukemia and lymphoma, yet manual interpretation of BM smear slides is labor-intensive for hematologists and pathologists. Few automatic diagnostic tools have successfully classified whole slide images (WSIs) of hematologic malignancies. This study aimed to develop a deep convolutional neural network (DCNN) pipeline to classify leukemia subtypes and lymphoma using whole-slide BM aspirate images. Methods: The process involved two stages: first, a quality assessment model selected 200 regions of interest (ROIs) from each WSI to exclude non-informative areas. Next, eight DCNN models with different architectures were trained to classify each ROI into one of five hematologic malignancies, and tile-level predictions were aggregated to produce patient-level results. External evaluation and ancillary analyses were performed to demonstrate generalizability and robustness. Results: In total, 1,022 WSIs were enrolled. The results showed average patient-level accuracy, balanced accuracy, F1-score, and area under the receiver operating characteristic curve (AUC) of 95.2%, 94.7%, 94.8%, and 0.993, respectively, with DenseNet121 achieving the highest balanced accuracy (97.6%). Our method outperformed clustering-constrained attention multiple instance learning (CLAM) in comparison study (accuracy 97.1% vs. 85.0%) and reached accuracies of 83.8% and 86.7% on external datasets. Visualization maps showed consistency between model salience and cell distribution. Conclusion: Our results demonstrate the ability of DCNNs to achieve accurate diagnosis in hematologic pathology, and the pipeline holds potential to assist in early diagnosis and workflow augmentation for hematologists and pathologists.

Indexed as

deep convolutional neural networkhematologic malignancymultiple instance learningwhole slide image

Identifiers

PMID42052410
PMCPMC13111881

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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.