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MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study

BACKGROUND AND PURPOSE: Predicting tumour response would be useful for selecting patients with locally advanced rectal cancer (LARC) for organ preservation strategies. We aimed to develop and validate a prediction model for T downstaging (ypT0-2) in LARC patients after neoadjuvant chemoradiotherapy...

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Autores principales: Xiang, Yirong, Li, Shuai, Wang, Hongzhi, Song, Maxiaowei, Hu, Ke, Wang, Fengwei, Wang, Zhi, Niu, Zhiyong, Liu, Jin, Cai, Yong, Li, Yongheng, Zhu, Xianggao, Geng, Jianhao, Zhang, Yangzi, Teng, Huajing, Wang, Weihu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719068/
https://www.ncbi.nlm.nih.gov/pubmed/36471751
http://dx.doi.org/10.1016/j.ctro.2022.11.009
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author Xiang, Yirong
Li, Shuai
Wang, Hongzhi
Song, Maxiaowei
Hu, Ke
Wang, Fengwei
Wang, Zhi
Niu, Zhiyong
Liu, Jin
Cai, Yong
Li, Yongheng
Zhu, Xianggao
Geng, Jianhao
Zhang, Yangzi
Teng, Huajing
Wang, Weihu
author_facet Xiang, Yirong
Li, Shuai
Wang, Hongzhi
Song, Maxiaowei
Hu, Ke
Wang, Fengwei
Wang, Zhi
Niu, Zhiyong
Liu, Jin
Cai, Yong
Li, Yongheng
Zhu, Xianggao
Geng, Jianhao
Zhang, Yangzi
Teng, Huajing
Wang, Weihu
author_sort Xiang, Yirong
collection PubMed
description BACKGROUND AND PURPOSE: Predicting tumour response would be useful for selecting patients with locally advanced rectal cancer (LARC) for organ preservation strategies. We aimed to develop and validate a prediction model for T downstaging (ypT0-2) in LARC patients after neoadjuvant chemoradiotherapy and to identify those who may benefit from consolidation chemotherapy. MATERIALS AND METHODS: cT3-4 LARC patients at three tertiary medical centers from January 2012 to January 2019 were retrospectively included, while a prospective cohort was recruited from June 2021 to March 2022. Eight filter (principal component analysis, least absolute shrinkage and selection operator, partial least-squares discriminant analysis, random forest)-classifier (support vector machine, logistic regression) models were established to select radiomic features. A nomogram combining radiomics and significant clinical features was developed and validated by calibration curve and decision curve analysis. Interaction test was conducted to investigate the consolidation chemotherapy benefits. RESULTS: A total of 634 patients were included (426 in training cohort, 174 in testing cohort and 34 in prospective cohort). A radiomic prediction model using partial least-squares discriminant analysis and a support vector machine showed the best performance (AUC: 0.832 [training]; 0.763 [testing]). A nomogram combining radiomics and clinical features showed significantly better prognostic performance (AUC: 0.842 [training]; 0.809 [testing]) than the radiomic model. The model was also tested in the prospective cohort with AUC 0.727. High-probability group (score > 81.82) may have potential benefits from ≥ 4 cycles consolidation chemotherapy (OR: 4.173, 95 % CI: 0.953–18.276, p = 0.058, p(interaction) = 0.021). CONCLUSION: We identified and validated a model based on multicenter pre-treatment radiomics to predict ypT0-2 in cT3-4 LARC patients, which may facilitate individualised treatment decision-making for organ-preservation strategies and consolidation chemotherapy.
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spelling pubmed-97190682022-12-04 MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study Xiang, Yirong Li, Shuai Wang, Hongzhi Song, Maxiaowei Hu, Ke Wang, Fengwei Wang, Zhi Niu, Zhiyong Liu, Jin Cai, Yong Li, Yongheng Zhu, Xianggao Geng, Jianhao Zhang, Yangzi Teng, Huajing Wang, Weihu Clin Transl Radiat Oncol Article BACKGROUND AND PURPOSE: Predicting tumour response would be useful for selecting patients with locally advanced rectal cancer (LARC) for organ preservation strategies. We aimed to develop and validate a prediction model for T downstaging (ypT0-2) in LARC patients after neoadjuvant chemoradiotherapy and to identify those who may benefit from consolidation chemotherapy. MATERIALS AND METHODS: cT3-4 LARC patients at three tertiary medical centers from January 2012 to January 2019 were retrospectively included, while a prospective cohort was recruited from June 2021 to March 2022. Eight filter (principal component analysis, least absolute shrinkage and selection operator, partial least-squares discriminant analysis, random forest)-classifier (support vector machine, logistic regression) models were established to select radiomic features. A nomogram combining radiomics and significant clinical features was developed and validated by calibration curve and decision curve analysis. Interaction test was conducted to investigate the consolidation chemotherapy benefits. RESULTS: A total of 634 patients were included (426 in training cohort, 174 in testing cohort and 34 in prospective cohort). A radiomic prediction model using partial least-squares discriminant analysis and a support vector machine showed the best performance (AUC: 0.832 [training]; 0.763 [testing]). A nomogram combining radiomics and clinical features showed significantly better prognostic performance (AUC: 0.842 [training]; 0.809 [testing]) than the radiomic model. The model was also tested in the prospective cohort with AUC 0.727. High-probability group (score > 81.82) may have potential benefits from ≥ 4 cycles consolidation chemotherapy (OR: 4.173, 95 % CI: 0.953–18.276, p = 0.058, p(interaction) = 0.021). CONCLUSION: We identified and validated a model based on multicenter pre-treatment radiomics to predict ypT0-2 in cT3-4 LARC patients, which may facilitate individualised treatment decision-making for organ-preservation strategies and consolidation chemotherapy. Elsevier 2022-11-17 /pmc/articles/PMC9719068/ /pubmed/36471751 http://dx.doi.org/10.1016/j.ctro.2022.11.009 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Xiang, Yirong
Li, Shuai
Wang, Hongzhi
Song, Maxiaowei
Hu, Ke
Wang, Fengwei
Wang, Zhi
Niu, Zhiyong
Liu, Jin
Cai, Yong
Li, Yongheng
Zhu, Xianggao
Geng, Jianhao
Zhang, Yangzi
Teng, Huajing
Wang, Weihu
MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study
title MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study
title_full MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study
title_fullStr MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study
title_full_unstemmed MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study
title_short MRI-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: A multicenter study
title_sort mri-based radiomics to predict neoadjuvant chemoradiotherapy outcomes in locally advanced rectal cancer: a multicenter study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719068/
https://www.ncbi.nlm.nih.gov/pubmed/36471751
http://dx.doi.org/10.1016/j.ctro.2022.11.009
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