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Comprehensive performance assessment of the BMIA-12 a system for bone marrow cell quantification in normal and hematological malignancy samples.

Scientific reports 2026 Vol.16(1)

Kim HN, Lee JH, Jung Y, Kwon JA, Yoon SY

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[UNLABELLED] Manual bone marrow (BM) differential counting is labor-intensive, time-consuming, and prone to inter-observer variability.

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APA Kim HN, Lee JH, et al. (2026). Comprehensive performance assessment of the BMIA-12 a system for bone marrow cell quantification in normal and hematological malignancy samples.. Scientific reports, 16(1). https://doi.org/10.1038/s41598-026-39443-1
MLA Kim HN, et al.. "Comprehensive performance assessment of the BMIA-12 a system for bone marrow cell quantification in normal and hematological malignancy samples.." Scientific reports, vol. 16, no. 1, 2026.
PMID 41688743

Abstract

[UNLABELLED] Manual bone marrow (BM) differential counting is labor-intensive, time-consuming, and prone to inter-observer variability. Artificial intelligence (AI)-based systems can standardize BM cytological assessments. This study evaluated the BMIA-12 A system (UIMD, Seoul, Korea) for automated BM cell recognition and differential counting. A total of 298 BM aspirate smears from 149 patients were analyzed, including normal controls ( = 50), multiple myeloma ( = 33), monoclonal gammopathy of undetermined significance ( = 6), acute myeloid leukemia (AML;  = 40), acute promyelocytic leukemia ( = 4), and acute lymphoblastic leukemia (ALL;  = 16). Three classification methods were compared: AI-automated, expert-reviewed AI, and manual microscopic counting. Both wedge and squash preparations were assessed. System performance was evaluated using recall, precision, F1-score, and accuracy. BMIA-12 A achieved accuracies of 94.6% (wedge) and 94.0% (squash), with recall > 90% for 14/16 cell types. Wedge preparations showed superior precision for key diagnostic cells, including plasma cells, blasts, and basophils. Strong correlations ( ≥ 0.9) were observed between AI-automated and expert-reviewed classifications for nine cell types. However, disease-specific quantification varied significantly by method, particularly for plasma cell and blast percentages. Inter-method discrepancies were pronounced in AML with mutation and B-ALL with fusion. Overall, BMIA-12 A provides robust classification for normal BM samples. Persistent inter-method differences highlight the need for further validation.

[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1038/s41598-026-39443-1.

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