Artificial Intelligence Enhances Diagnostic Flow Cytometry Workflow in the Detection of Minimal Residual Disease of Chronic Lymphocytic Leukemia.
Mohamed E SalamaGregory E OttesonJon J CampJansen N SeheultDragan JevremovicDavid R HolmesHoratiu OlteanuMin ShiPublished in: Cancers (2022)
Flow cytometric (FC) immunophenotyping is critical but time-consuming in diagnosing minimal residual disease (MRD). We evaluated whether human-in-the-loop artificial intelligence (AI) could improve the efficiency of clinical laboratories in detecting MRD in chronic lymphocytic leukemia (CLL). We developed deep neural networks (DNN) that were trained on a 10-color CLL MRD panel from treated CLL patients, including DNN trained on the full cohort of 202 patients (F-DNN) and DNN trained on 138 patients with low-event cases (MRD < 1000 events) (L-DNN). A hybrid DNN approach was utilized, with F-DNN and L-DNN applied sequentially to cases. "Ground truth" classification of CLL MRD was confirmed by expert analysis. The hybrid DNN approach demonstrated an overall accuracy of 97.1% (95% CI: 84.7-99.9%) in an independent cohort of 34 unknown samples. When CLL cells were reported as a percentage of total white blood cells, there was excellent correlation between the DNN and expert analysis [r > 0.999; Passing-Bablok slope = 0.997 (95% CI: 0.988-0.999) and intercept = 0.001 (95% CI: 0.000-0.001)]. Gating time was dramatically reduced to 12 s/case by DNN from 15 min/case by the manual process. The proposed DNN demonstrated high accuracy in CLL MRD detection and significantly improved workflow efficiency. Additional clinical validation is needed before it can be fully integrated into the existing clinical laboratory practice.
Keyphrases
- chronic lymphocytic leukemia
- artificial intelligence
- machine learning
- deep learning
- end stage renal disease
- flow cytometry
- big data
- newly diagnosed
- chronic kidney disease
- induced apoptosis
- primary care
- peritoneal dialysis
- endothelial cells
- neural network
- patient reported outcomes
- loop mediated isothermal amplification
- quality improvement
- induced pluripotent stem cells