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Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data
Medical imaging represents the primary tool for investigating and monitoring several diseases, including cancer. The advances in quantitative image analysis have developed towards the extraction of biomarkers able to support clinical decisions. To produce robust results, multi-center studies are oft...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620174/ https://www.ncbi.nlm.nih.gov/pubmed/37914758 http://dx.doi.org/10.1038/s41598-023-45983-7 |
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author | Cavinato, Lara Massi, Michela Carlotta Sollini, Martina Kirienko, Margarita Ieva, Francesca |
author_facet | Cavinato, Lara Massi, Michela Carlotta Sollini, Martina Kirienko, Margarita Ieva, Francesca |
author_sort | Cavinato, Lara |
collection | PubMed |
description | Medical imaging represents the primary tool for investigating and monitoring several diseases, including cancer. The advances in quantitative image analysis have developed towards the extraction of biomarkers able to support clinical decisions. To produce robust results, multi-center studies are often set up. However, the imaging information must be denoised from confounding factors—known as batch-effect—like scanner-specific and center-specific influences. Moreover, in non-solid cancers, like lymphomas, effective biomarkers require an imaging-based representation of the disease that accounts for its multi-site spreading over the patient’s body. In this work, we address the dual-factor deconfusion problem and we propose a deconfusion algorithm to harmonize the imaging information of patients affected by Hodgkin Lymphoma in a multi-center setting. We show that the proposed model successfully denoises data from domain-specific variability (p-value < 0.001) while it coherently preserves the spatial relationship between imaging descriptions of peer lesions (p-value = 0), which is a strong prognostic biomarker for tumor heterogeneity assessment. This harmonization step allows to significantly improve the performance in prognostic models with respect to state-of-the-art methods, enabling building exhaustive patient representations and delivering more accurate analyses (p-values < 0.001 in training, p-values < 0.05 in testing). This work lays the groundwork for performing large-scale and reproducible analyses on multi-center data that are urgently needed to convey the translation of imaging-based biomarkers into the clinical practice as effective prognostic tools. The code is available on GitHub at this https://github.com/LaraCavinato/Dual-ADAE. |
format | Online Article Text |
id | pubmed-10620174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106201742023-11-03 Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data Cavinato, Lara Massi, Michela Carlotta Sollini, Martina Kirienko, Margarita Ieva, Francesca Sci Rep Article Medical imaging represents the primary tool for investigating and monitoring several diseases, including cancer. The advances in quantitative image analysis have developed towards the extraction of biomarkers able to support clinical decisions. To produce robust results, multi-center studies are often set up. However, the imaging information must be denoised from confounding factors—known as batch-effect—like scanner-specific and center-specific influences. Moreover, in non-solid cancers, like lymphomas, effective biomarkers require an imaging-based representation of the disease that accounts for its multi-site spreading over the patient’s body. In this work, we address the dual-factor deconfusion problem and we propose a deconfusion algorithm to harmonize the imaging information of patients affected by Hodgkin Lymphoma in a multi-center setting. We show that the proposed model successfully denoises data from domain-specific variability (p-value < 0.001) while it coherently preserves the spatial relationship between imaging descriptions of peer lesions (p-value = 0), which is a strong prognostic biomarker for tumor heterogeneity assessment. This harmonization step allows to significantly improve the performance in prognostic models with respect to state-of-the-art methods, enabling building exhaustive patient representations and delivering more accurate analyses (p-values < 0.001 in training, p-values < 0.05 in testing). This work lays the groundwork for performing large-scale and reproducible analyses on multi-center data that are urgently needed to convey the translation of imaging-based biomarkers into the clinical practice as effective prognostic tools. The code is available on GitHub at this https://github.com/LaraCavinato/Dual-ADAE. Nature Publishing Group UK 2023-11-01 /pmc/articles/PMC10620174/ /pubmed/37914758 http://dx.doi.org/10.1038/s41598-023-45983-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Cavinato, Lara Massi, Michela Carlotta Sollini, Martina Kirienko, Margarita Ieva, Francesca Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
title | Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
title_full | Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
title_fullStr | Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
title_full_unstemmed | Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
title_short | Dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
title_sort | dual adversarial deconfounding autoencoder for joint batch-effects removal from multi-center and multi-scanner radiomics data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620174/ https://www.ncbi.nlm.nih.gov/pubmed/37914758 http://dx.doi.org/10.1038/s41598-023-45983-7 |
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