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Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC
Recurrence occurs in up to 36% of patients treated with curative-intent radiotherapy for NSCLC. Identifying patients at higher risk of recurrence for more intensive surveillance may facilitate the earlier introduction of the next line of treatment. We aimed to use radiotherapy planning CT scans to d...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613990/ https://www.ncbi.nlm.nih.gov/pubmed/36302938 http://dx.doi.org/10.1038/s41698-022-00322-3 |
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author | Hindocha, Sumeet Charlton, Thomas G. Linton-Reid, Kristofer Hunter, Benjamin Chan, Charleen Ahmed, Merina Greenlay, Emily J. Orton, Matthew Bunce, Catey Lunn, Jason Doran, Simon J. Ahmad, Shahreen McDonald, Fiona Locke, Imogen Power, Danielle Blackledge, Matthew Lee, Richard W. Aboagye, Eric O. |
author_facet | Hindocha, Sumeet Charlton, Thomas G. Linton-Reid, Kristofer Hunter, Benjamin Chan, Charleen Ahmed, Merina Greenlay, Emily J. Orton, Matthew Bunce, Catey Lunn, Jason Doran, Simon J. Ahmad, Shahreen McDonald, Fiona Locke, Imogen Power, Danielle Blackledge, Matthew Lee, Richard W. Aboagye, Eric O. |
author_sort | Hindocha, Sumeet |
collection | PubMed |
description | Recurrence occurs in up to 36% of patients treated with curative-intent radiotherapy for NSCLC. Identifying patients at higher risk of recurrence for more intensive surveillance may facilitate the earlier introduction of the next line of treatment. We aimed to use radiotherapy planning CT scans to develop radiomic classification models that predict overall survival (OS), recurrence-free survival (RFS) and recurrence two years post-treatment for risk-stratification. A retrospective multi-centre study of >900 patients receiving curative-intent radiotherapy for stage I-III NSCLC was undertaken. Models using radiomic and/or clinical features were developed, compared with 10-fold cross-validation and an external test set, and benchmarked against TNM-stage. Respective validation and test set AUCs (with 95% confidence intervals) for the radiomic-only models were: (1) OS: 0.712 (0.592–0.832) and 0.685 (0.585–0.784), (2) RFS: 0.825 (0.733–0.916) and 0.750 (0.665–0.835), (3) Recurrence: 0.678 (0.554–0.801) and 0.673 (0.577–0.77). For the combined models: (1) OS: 0.702 (0.583–0.822) and 0.683 (0.586–0.78), (2) RFS: 0.805 (0.707–0.903) and 0·755 (0.672–0.838), (3) Recurrence: 0·637 (0.51–0.·765) and 0·738 (0.649–0.826). Kaplan-Meier analyses demonstrate OS and RFS difference of >300 and >400 days respectively between low and high-risk groups. We have developed validated and externally tested radiomic-based prediction models. Such models could be integrated into the routine radiotherapy workflow, thus informing a personalised surveillance strategy at the point of treatment. Our work lays the foundations for future prospective clinical trials for quantitative personalised risk-stratification for surveillance following curative-intent radiotherapy for NSCLC. |
format | Online Article Text |
id | pubmed-9613990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96139902022-10-29 Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC Hindocha, Sumeet Charlton, Thomas G. Linton-Reid, Kristofer Hunter, Benjamin Chan, Charleen Ahmed, Merina Greenlay, Emily J. Orton, Matthew Bunce, Catey Lunn, Jason Doran, Simon J. Ahmad, Shahreen McDonald, Fiona Locke, Imogen Power, Danielle Blackledge, Matthew Lee, Richard W. Aboagye, Eric O. NPJ Precis Oncol Article Recurrence occurs in up to 36% of patients treated with curative-intent radiotherapy for NSCLC. Identifying patients at higher risk of recurrence for more intensive surveillance may facilitate the earlier introduction of the next line of treatment. We aimed to use radiotherapy planning CT scans to develop radiomic classification models that predict overall survival (OS), recurrence-free survival (RFS) and recurrence two years post-treatment for risk-stratification. A retrospective multi-centre study of >900 patients receiving curative-intent radiotherapy for stage I-III NSCLC was undertaken. Models using radiomic and/or clinical features were developed, compared with 10-fold cross-validation and an external test set, and benchmarked against TNM-stage. Respective validation and test set AUCs (with 95% confidence intervals) for the radiomic-only models were: (1) OS: 0.712 (0.592–0.832) and 0.685 (0.585–0.784), (2) RFS: 0.825 (0.733–0.916) and 0.750 (0.665–0.835), (3) Recurrence: 0.678 (0.554–0.801) and 0.673 (0.577–0.77). For the combined models: (1) OS: 0.702 (0.583–0.822) and 0.683 (0.586–0.78), (2) RFS: 0.805 (0.707–0.903) and 0·755 (0.672–0.838), (3) Recurrence: 0·637 (0.51–0.·765) and 0·738 (0.649–0.826). Kaplan-Meier analyses demonstrate OS and RFS difference of >300 and >400 days respectively between low and high-risk groups. We have developed validated and externally tested radiomic-based prediction models. Such models could be integrated into the routine radiotherapy workflow, thus informing a personalised surveillance strategy at the point of treatment. Our work lays the foundations for future prospective clinical trials for quantitative personalised risk-stratification for surveillance following curative-intent radiotherapy for NSCLC. Nature Publishing Group UK 2022-10-27 /pmc/articles/PMC9613990/ /pubmed/36302938 http://dx.doi.org/10.1038/s41698-022-00322-3 Text en © The Author(s) 2022, corrected publication 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hindocha, Sumeet Charlton, Thomas G. Linton-Reid, Kristofer Hunter, Benjamin Chan, Charleen Ahmed, Merina Greenlay, Emily J. Orton, Matthew Bunce, Catey Lunn, Jason Doran, Simon J. Ahmad, Shahreen McDonald, Fiona Locke, Imogen Power, Danielle Blackledge, Matthew Lee, Richard W. Aboagye, Eric O. Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC |
title | Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC |
title_full | Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC |
title_fullStr | Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC |
title_full_unstemmed | Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC |
title_short | Gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for NSCLC |
title_sort | gross tumour volume radiomics for prognostication of recurrence & death following radical radiotherapy for nsclc |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613990/ https://www.ncbi.nlm.nih.gov/pubmed/36302938 http://dx.doi.org/10.1038/s41698-022-00322-3 |
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