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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7213640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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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