TY - JOUR
T1 - Identification and staging of B-cell acute lymphoblastic leukemia using quantitative phase imaging and machine learning
AU - Ayyappan, Vinay
AU - Chang, Alex
AU - Zhang, Chi
AU - Paidi, Santosh Kumar
AU - Bordett, Rosalie
AU - Liang, Tiffany
AU - Barman, Ishan
AU - Pandey, Rishikesh
N1 - Publisher Copyright:
© 2020 American Chemical Society. All rights reserved.
PY - 2020/10/23
Y1 - 2020/10/23
N2 - Identification and classification of leukemia cells in a rapid and label-free fashion is clinically challenging and thus presents a prime arena for implementing new diagnostic tools. Quantitative phase imaging, which maps optical path length delays introduced by the specimen, has been demonstrated to discern cellular phenotypes based on differential morphological attributes. Rapid acquisition capability and the availability of label-free images with high information content have enabled researchers to use machine learning (ML) to reveal latent features. We developed a set of ML classifiers, including convolutional neural networks, to discern healthy B cells from lymphoblasts and classify stages of B cell acute lymphoblastic leukemia. Here, we show that the average dry mass and volume of normal B cells are lower than those of cancerous cells and that these morphologic parameters increase further alongside disease progression. We find that the relaxed training requirements of a ML approach are conducive to the classification of cell type, with minimal space, training time, and memory requirements. Our findings pave the way for a larger study on clinical samples of acute lymphoblastic leukemia, with the overarching goal of its broader use in hematopathology, where the prospect of objective diagnoses with minimal sample preparation remains highly desirable.
AB - Identification and classification of leukemia cells in a rapid and label-free fashion is clinically challenging and thus presents a prime arena for implementing new diagnostic tools. Quantitative phase imaging, which maps optical path length delays introduced by the specimen, has been demonstrated to discern cellular phenotypes based on differential morphological attributes. Rapid acquisition capability and the availability of label-free images with high information content have enabled researchers to use machine learning (ML) to reveal latent features. We developed a set of ML classifiers, including convolutional neural networks, to discern healthy B cells from lymphoblasts and classify stages of B cell acute lymphoblastic leukemia. Here, we show that the average dry mass and volume of normal B cells are lower than those of cancerous cells and that these morphologic parameters increase further alongside disease progression. We find that the relaxed training requirements of a ML approach are conducive to the classification of cell type, with minimal space, training time, and memory requirements. Our findings pave the way for a larger study on clinical samples of acute lymphoblastic leukemia, with the overarching goal of its broader use in hematopathology, where the prospect of objective diagnoses with minimal sample preparation remains highly desirable.
KW - Classification
KW - Deep learning
KW - Label-free imaging
KW - Leukemia
KW - Quantitative phase imaging
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U2 - 10.1021/acssensors.0c01811
DO - 10.1021/acssensors.0c01811
M3 - Article
C2 - 33092347
AN - SCOPUS:85094605814
SN - 2379-3694
VL - 5
SP - 3281
EP - 3289
JO - ACS sensors
JF - ACS sensors
IS - 10
ER -