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Label‐Free Leukemia Monitoring by Computer Vision

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) 1913–19...

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Autores principales: Doan, Minh, Case, Marian, Masic, Dino, Hennig, Holger, McQuin, Claire, Caicedo, Juan, Singh, Shantanu, Goodman, Allen, Wolkenhauer, Olaf, Summers, Huw D., Jamieson, David, van Delft, Frederik W, Filby, Andrew, Carpenter, Anne E., Rees, Paul, Irving, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213640/
https://www.ncbi.nlm.nih.gov/pubmed/32091180
http://dx.doi.org/10.1002/cyto.a.23987
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author Doan, Minh
Case, Marian
Masic, Dino
Hennig, Holger
McQuin, Claire
Caicedo, Juan
Singh, Shantanu
Goodman, Allen
Wolkenhauer, Olaf
Summers, Huw D.
Jamieson, David
van Delft, Frederik W
Filby, Andrew
Carpenter, Anne E.
Rees, Paul
Irving, Julie
author_facet Doan, Minh
Case, Marian
Masic, Dino
Hennig, Holger
McQuin, Claire
Caicedo, Juan
Singh, Shantanu
Goodman, Allen
Wolkenhauer, Olaf
Summers, Huw D.
Jamieson, David
van Delft, Frederik W
Filby, Andrew
Carpenter, Anne E.
Rees, Paul
Irving, Julie
author_sort Doan, Minh
collection PubMed
description 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. © 2020 The Authors. Cytometry Part A published by Wiley Periodicals, Inc. on behalf of International Society for Advancement of Cytometry.
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spelling pubmed-72136402020-07-27 Label‐Free Leukemia Monitoring by Computer Vision Doan, Minh Case, Marian Masic, Dino Hennig, Holger McQuin, Claire Caicedo, Juan Singh, Shantanu Goodman, Allen Wolkenhauer, Olaf Summers, Huw D. Jamieson, David van Delft, Frederik W Filby, Andrew Carpenter, Anne E. Rees, Paul Irving, Julie Cytometry A Brief Report 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. © 2020 The Authors. Cytometry Part A published by Wiley Periodicals, Inc. on behalf of International Society for Advancement of Cytometry. John Wiley & Sons, Inc. 2020-02-24 2020-04 /pmc/articles/PMC7213640/ /pubmed/32091180 http://dx.doi.org/10.1002/cyto.a.23987 Text en © 2020 The Authors. Cytometry Part A published by Wiley Periodicals, Inc. on behalf of International Society for Advancement of Cytometry. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Doan, Minh
Case, Marian
Masic, Dino
Hennig, Holger
McQuin, Claire
Caicedo, Juan
Singh, Shantanu
Goodman, Allen
Wolkenhauer, Olaf
Summers, Huw D.
Jamieson, David
van Delft, Frederik W
Filby, Andrew
Carpenter, Anne E.
Rees, Paul
Irving, Julie
Label‐Free Leukemia Monitoring by Computer Vision
title Label‐Free Leukemia Monitoring by Computer Vision
title_full Label‐Free Leukemia Monitoring by Computer Vision
title_fullStr Label‐Free Leukemia Monitoring by Computer Vision
title_full_unstemmed Label‐Free Leukemia Monitoring by Computer Vision
title_short Label‐Free Leukemia Monitoring by Computer Vision
title_sort label‐free leukemia monitoring by computer vision
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213640/
https://www.ncbi.nlm.nih.gov/pubmed/32091180
http://dx.doi.org/10.1002/cyto.a.23987
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