| Literature DB >> 32091180 |
Minh Doan1, Marian Case2, Dino Masic2, Holger Hennig1,3, Claire McQuin1, Juan Caicedo1, Shantanu Singh1, Allen Goodman1, Olaf Wolkenhauer3, Huw D Summers4, David Jamieson2, Frederik V Delft2, Andrew Filby5, Anne E Carpenter1, Paul Rees1,4, Julie Irving2.
Abstract
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. While there are a number of well-recognized prognostic biomarkers at diagnosis, the most powerful independent prognostic factor is the response of the leukemia to induction chemotherapy (Campana and Pui: Blood 129 (2017) 1913-1918). Given the potential for machine learning to improve precision medicine, we tested its capacity to monitor disease in children undergoing ALL treatment. Diagnostic and on-treatment bone marrow samples were labeled with an ALL-discriminating antibody combination and analyzed by imaging flow cytometry. Ignoring the fluorescent markers and using only features extracted from bright-field and dark-field cell images, a deep learning model was able to identify ALL cells at an accuracy of >88%. This antibody-free, single cell method is cheap, quick, and could be adapted to a simple, laser-free cytometer to allow automated, point-of-care testing to detect slow early responders. Adaptation to other types of leukemia is feasible, which would revolutionize residual disease monitoring.Entities:
Keywords: computer vision; deep learning; imaging flow cytometry; label-free; leukemia; machine learning; neural networks
Year: 2020 PMID: 32091180 DOI: 10.1002/cyto.a.23987
Source DB: PubMed Journal: Cytometry A ISSN: 1552-4922 Impact factor: 4.355