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MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance

Nearly half of patients with prostate cancer (PCa) harbour low- or intermediate-risk disease considered suitable for active surveillance (AS). However, up to 44% of patients discontinue AS within the first five years, highlighting the unmet clinical need for robust baseline risk-stratification tools...

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Autores principales: Sushentsev, Nikita, Rundo, Leonardo, Blyuss, Oleg, Gnanapragasam, Vincent J., Sala, Evis, Barrett, Tristan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217549/
https://www.ncbi.nlm.nih.gov/pubmed/34155265
http://dx.doi.org/10.1038/s41598-021-92341-6
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author Sushentsev, Nikita
Rundo, Leonardo
Blyuss, Oleg
Gnanapragasam, Vincent J.
Sala, Evis
Barrett, Tristan
author_facet Sushentsev, Nikita
Rundo, Leonardo
Blyuss, Oleg
Gnanapragasam, Vincent J.
Sala, Evis
Barrett, Tristan
author_sort Sushentsev, Nikita
collection PubMed
description Nearly half of patients with prostate cancer (PCa) harbour low- or intermediate-risk disease considered suitable for active surveillance (AS). However, up to 44% of patients discontinue AS within the first five years, highlighting the unmet clinical need for robust baseline risk-stratification tools that enable timely and accurate prediction of tumour progression. In this proof-of-concept study, we sought to investigate the added value of MRI-derived radiomic features to standard-of-care clinical parameters for improving baseline prediction of PCa progression in AS patients. Tumour T(2)-weighted imaging (T2WI) and apparent diffusion coefficient radiomic features were extracted, with rigorous calibration and pre-processing methods applied to select the most robust features for predictive modelling. Following leave-one-out cross-validation, the addition of T2WI-derived radiomic features to clinical variables alone improved the area under the ROC curve for predicting progression from 0.61 (95% confidence interval [CI] 0.481–0.743) to 0.75 (95% CI 0.64–0.86). These exploratory findings demonstrate the potential benefit of MRI-derived radiomics to add incremental benefit to clinical data only models in the baseline prediction of PCa progression on AS, paving the way for future multicentre studies validating the proposed model and evaluating its impact on clinical outcomes.
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spelling pubmed-82175492021-06-22 MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance Sushentsev, Nikita Rundo, Leonardo Blyuss, Oleg Gnanapragasam, Vincent J. Sala, Evis Barrett, Tristan Sci Rep Article Nearly half of patients with prostate cancer (PCa) harbour low- or intermediate-risk disease considered suitable for active surveillance (AS). However, up to 44% of patients discontinue AS within the first five years, highlighting the unmet clinical need for robust baseline risk-stratification tools that enable timely and accurate prediction of tumour progression. In this proof-of-concept study, we sought to investigate the added value of MRI-derived radiomic features to standard-of-care clinical parameters for improving baseline prediction of PCa progression in AS patients. Tumour T(2)-weighted imaging (T2WI) and apparent diffusion coefficient radiomic features were extracted, with rigorous calibration and pre-processing methods applied to select the most robust features for predictive modelling. Following leave-one-out cross-validation, the addition of T2WI-derived radiomic features to clinical variables alone improved the area under the ROC curve for predicting progression from 0.61 (95% confidence interval [CI] 0.481–0.743) to 0.75 (95% CI 0.64–0.86). These exploratory findings demonstrate the potential benefit of MRI-derived radiomics to add incremental benefit to clinical data only models in the baseline prediction of PCa progression on AS, paving the way for future multicentre studies validating the proposed model and evaluating its impact on clinical outcomes. Nature Publishing Group UK 2021-06-21 /pmc/articles/PMC8217549/ /pubmed/34155265 http://dx.doi.org/10.1038/s41598-021-92341-6 Text en © The Author(s) 2021 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
Sushentsev, Nikita
Rundo, Leonardo
Blyuss, Oleg
Gnanapragasam, Vincent J.
Sala, Evis
Barrett, Tristan
MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
title MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
title_full MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
title_fullStr MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
title_full_unstemmed MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
title_short MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
title_sort mri-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217549/
https://www.ncbi.nlm.nih.gov/pubmed/34155265
http://dx.doi.org/10.1038/s41598-021-92341-6
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