Cargando…

Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach

Accurate characterization of microcalcifications (MCs) in 2D digital mammography is a necessary step toward reducing the diagnostic uncertainty associated with the callback of indeterminate MCs. Quantitative analysis of MCs can better identify MCs with a higher likelihood of ductal carcinoma in situ...

Descripción completa

Detalles Bibliográficos
Autores principales: Marasinou, Chrysostomos, Li, Bo, Paige, Jeremy, Omigbodun, Akinyinka, Nakhaei, Noor, Hoyt, Anne, Hsu, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287598/
https://www.ncbi.nlm.nih.gov/pubmed/36820930
http://dx.doi.org/10.1007/s10278-022-00751-3
_version_ 1785061908241448960
author Marasinou, Chrysostomos
Li, Bo
Paige, Jeremy
Omigbodun, Akinyinka
Nakhaei, Noor
Hoyt, Anne
Hsu, William
author_facet Marasinou, Chrysostomos
Li, Bo
Paige, Jeremy
Omigbodun, Akinyinka
Nakhaei, Noor
Hoyt, Anne
Hsu, William
author_sort Marasinou, Chrysostomos
collection PubMed
description Accurate characterization of microcalcifications (MCs) in 2D digital mammography is a necessary step toward reducing the diagnostic uncertainty associated with the callback of indeterminate MCs. Quantitative analysis of MCs can better identify MCs with a higher likelihood of ductal carcinoma in situ or invasive cancer. However, automated identification and segmentation of MCs remain challenging with high false positive rates. We present a two-stage multiscale approach to MC segmentation in 2D full-field digital mammograms (FFDMs) and diagnostic magnification views. Candidate objects are first delineated using blob detection and Hessian analysis. A regression convolutional network, trained to output a function with a higher response near MCs, chooses the objects which constitute actual MCs. The method was trained and validated on 435 screening and diagnostic FFDMs from two separate datasets. We then used our approach to segment MCs on magnification views of 248 cases with amorphous MCs. We modeled the extracted features using gradient tree boosting to classify each case as benign or malignant. Compared to state-of-the-art comparison methods, our approach achieved superior mean intersection over the union (0.670 ± 0.121 per image versus 0.524 ± 0.034 per image), intersection over the union per MC object (0.607 ± 0.250 versus 0.363 ± 0.278) and true positive rate of 0.744 versus 0.581 at 0.4 false positive detections per square centimeter. Features generated using our approach outperformed the comparison method (0.763 versus 0.710 AUC) in distinguishing amorphous calcifications as benign or malignant. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10278-022-00751-3.
format Online
Article
Text
id pubmed-10287598
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-102875982023-06-24 Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach Marasinou, Chrysostomos Li, Bo Paige, Jeremy Omigbodun, Akinyinka Nakhaei, Noor Hoyt, Anne Hsu, William J Digit Imaging Article Accurate characterization of microcalcifications (MCs) in 2D digital mammography is a necessary step toward reducing the diagnostic uncertainty associated with the callback of indeterminate MCs. Quantitative analysis of MCs can better identify MCs with a higher likelihood of ductal carcinoma in situ or invasive cancer. However, automated identification and segmentation of MCs remain challenging with high false positive rates. We present a two-stage multiscale approach to MC segmentation in 2D full-field digital mammograms (FFDMs) and diagnostic magnification views. Candidate objects are first delineated using blob detection and Hessian analysis. A regression convolutional network, trained to output a function with a higher response near MCs, chooses the objects which constitute actual MCs. The method was trained and validated on 435 screening and diagnostic FFDMs from two separate datasets. We then used our approach to segment MCs on magnification views of 248 cases with amorphous MCs. We modeled the extracted features using gradient tree boosting to classify each case as benign or malignant. Compared to state-of-the-art comparison methods, our approach achieved superior mean intersection over the union (0.670 ± 0.121 per image versus 0.524 ± 0.034 per image), intersection over the union per MC object (0.607 ± 0.250 versus 0.363 ± 0.278) and true positive rate of 0.744 versus 0.581 at 0.4 false positive detections per square centimeter. Features generated using our approach outperformed the comparison method (0.763 versus 0.710 AUC) in distinguishing amorphous calcifications as benign or malignant. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10278-022-00751-3. Springer International Publishing 2023-02-23 2023-06 /pmc/articles/PMC10287598/ /pubmed/36820930 http://dx.doi.org/10.1007/s10278-022-00751-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Marasinou, Chrysostomos
Li, Bo
Paige, Jeremy
Omigbodun, Akinyinka
Nakhaei, Noor
Hoyt, Anne
Hsu, William
Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach
title Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach
title_full Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach
title_fullStr Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach
title_full_unstemmed Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach
title_short Improving the Quantitative Analysis of Breast Microcalcifications: A Multiscale Approach
title_sort improving the quantitative analysis of breast microcalcifications: a multiscale approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287598/
https://www.ncbi.nlm.nih.gov/pubmed/36820930
http://dx.doi.org/10.1007/s10278-022-00751-3
work_keys_str_mv AT marasinouchrysostomos improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach
AT libo improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach
AT paigejeremy improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach
AT omigbodunakinyinka improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach
AT nakhaeinoor improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach
AT hoytanne improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach
AT hsuwilliam improvingthequantitativeanalysisofbreastmicrocalcificationsamultiscaleapproach