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Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction

SIMPLE SUMMARY: Machine learning approaches, using both radiomic and deep-learning-based features, were performed for an analysis of the breast parenchyma to identify women at risk of future breast cancer. Results from this study demonstrate that the antecedent mammographic images can potentially di...

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Autores principales: Li, Hui, Robinson, Kayla, Lan, Li, Baughan, Natalie, Chan, Chun-Wai, Embury, Matthew, Whitman, Gary J., El-Zein, Randa, Bedrosian, Isabelle, Giger, Maryellen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093086/
https://www.ncbi.nlm.nih.gov/pubmed/37046802
http://dx.doi.org/10.3390/cancers15072141
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author Li, Hui
Robinson, Kayla
Lan, Li
Baughan, Natalie
Chan, Chun-Wai
Embury, Matthew
Whitman, Gary J.
El-Zein, Randa
Bedrosian, Isabelle
Giger, Maryellen L.
author_facet Li, Hui
Robinson, Kayla
Lan, Li
Baughan, Natalie
Chan, Chun-Wai
Embury, Matthew
Whitman, Gary J.
El-Zein, Randa
Bedrosian, Isabelle
Giger, Maryellen L.
author_sort Li, Hui
collection PubMed
description SIMPLE SUMMARY: Machine learning approaches, using both radiomic and deep-learning-based features, were performed for an analysis of the breast parenchyma to identify women at risk of future breast cancer. Results from this study demonstrate that the antecedent mammographic images can potentially discriminate between women with a future-biopsy-proven cancer versus those with a future-biopsy-proven benign lesion. ABSTRACT: The identification of women at risk for sporadic breast cancer remains a clinical challenge. We hypothesize that the temporal analysis of annual screening mammograms, using a long short-term memory (LSTM) network, could accurately identify women at risk of future breast cancer. Women with an imaging abnormality, which had been biopsy-confirmed to be cancer or benign, who also had antecedent imaging available were included in this case–control study. Sequences of antecedent mammograms were retrospectively collected under HIPAA-approved guidelines. Radiomic and deep-learning-based features were extracted on regions of interest placed posterior to the nipple in antecedent images. These features were input to LSTM recurrent networks to classify whether the future lesion would be malignant or benign. Classification performance was assessed using all available antecedent time-points and using a single antecedent time-point in the task of lesion classification. Classifiers incorporating multiple time-points with LSTM, based either on deep-learning-extracted features or on radiomic features, tended to perform statistically better than chance, whereas those using only a single time-point failed to show improved performance compared to chance, as judged by area under the receiver operating characteristic curves (AUC: 0.63 ± 0.05, 0.65 ± 0.05, 0.52 ± 0.06 and 0.54 ± 0.06, respectively). Lastly, similar classification performance was observed when using features extracted from the affected versus the contralateral breast in predicting future unilateral malignancy (AUC: 0.63 ± 0.05 vs. 0.59 ± 0.06 for deep-learning-extracted features; 0.65 ± 0.05 vs. 0.62 ± 0.06 for radiomic features). The results of this study suggest that the incorporation of temporal information into radiomic analyses may improve the overall classification performance through LSTM, as demonstrated by the improved discrimination of future lesions as malignant or benign. Further, our data suggest that a potential field effect, changes in the breast extending beyond the lesion itself, is present in both the affected and contralateral breasts in antecedent imaging, and, thus, the evaluation of either breast might inform on the future risk of breast cancer.
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spelling pubmed-100930862023-04-13 Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction Li, Hui Robinson, Kayla Lan, Li Baughan, Natalie Chan, Chun-Wai Embury, Matthew Whitman, Gary J. El-Zein, Randa Bedrosian, Isabelle Giger, Maryellen L. Cancers (Basel) Article SIMPLE SUMMARY: Machine learning approaches, using both radiomic and deep-learning-based features, were performed for an analysis of the breast parenchyma to identify women at risk of future breast cancer. Results from this study demonstrate that the antecedent mammographic images can potentially discriminate between women with a future-biopsy-proven cancer versus those with a future-biopsy-proven benign lesion. ABSTRACT: The identification of women at risk for sporadic breast cancer remains a clinical challenge. We hypothesize that the temporal analysis of annual screening mammograms, using a long short-term memory (LSTM) network, could accurately identify women at risk of future breast cancer. Women with an imaging abnormality, which had been biopsy-confirmed to be cancer or benign, who also had antecedent imaging available were included in this case–control study. Sequences of antecedent mammograms were retrospectively collected under HIPAA-approved guidelines. Radiomic and deep-learning-based features were extracted on regions of interest placed posterior to the nipple in antecedent images. These features were input to LSTM recurrent networks to classify whether the future lesion would be malignant or benign. Classification performance was assessed using all available antecedent time-points and using a single antecedent time-point in the task of lesion classification. Classifiers incorporating multiple time-points with LSTM, based either on deep-learning-extracted features or on radiomic features, tended to perform statistically better than chance, whereas those using only a single time-point failed to show improved performance compared to chance, as judged by area under the receiver operating characteristic curves (AUC: 0.63 ± 0.05, 0.65 ± 0.05, 0.52 ± 0.06 and 0.54 ± 0.06, respectively). Lastly, similar classification performance was observed when using features extracted from the affected versus the contralateral breast in predicting future unilateral malignancy (AUC: 0.63 ± 0.05 vs. 0.59 ± 0.06 for deep-learning-extracted features; 0.65 ± 0.05 vs. 0.62 ± 0.06 for radiomic features). The results of this study suggest that the incorporation of temporal information into radiomic analyses may improve the overall classification performance through LSTM, as demonstrated by the improved discrimination of future lesions as malignant or benign. Further, our data suggest that a potential field effect, changes in the breast extending beyond the lesion itself, is present in both the affected and contralateral breasts in antecedent imaging, and, thus, the evaluation of either breast might inform on the future risk of breast cancer. MDPI 2023-04-04 /pmc/articles/PMC10093086/ /pubmed/37046802 http://dx.doi.org/10.3390/cancers15072141 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Hui
Robinson, Kayla
Lan, Li
Baughan, Natalie
Chan, Chun-Wai
Embury, Matthew
Whitman, Gary J.
El-Zein, Randa
Bedrosian, Isabelle
Giger, Maryellen L.
Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction
title Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction
title_full Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction
title_fullStr Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction
title_full_unstemmed Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction
title_short Temporal Machine Learning Analysis of Prior Mammograms for Breast Cancer Risk Prediction
title_sort temporal machine learning analysis of prior mammograms for breast cancer risk prediction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093086/
https://www.ncbi.nlm.nih.gov/pubmed/37046802
http://dx.doi.org/10.3390/cancers15072141
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