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(18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma

OBJECTIVE: To develop and validate an (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT)-based radiomics nomogram for non-invasively prediction of bone marrow involvement (BMI) in pediatric neuroblastoma. METHODS: A total of 133 patients with neuroblastoma were...

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Autores principales: Feng, Lijuan, Yang, Xu, Lu, Xia, Kan, Ying, Wang, Chao, Sun, Dehui, Zhang, Hui, Wang, Wei, Yang, Jigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440965/
https://www.ncbi.nlm.nih.gov/pubmed/36057694
http://dx.doi.org/10.1186/s13244-022-01283-8
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author Feng, Lijuan
Yang, Xu
Lu, Xia
Kan, Ying
Wang, Chao
Sun, Dehui
Zhang, Hui
Wang, Wei
Yang, Jigang
author_facet Feng, Lijuan
Yang, Xu
Lu, Xia
Kan, Ying
Wang, Chao
Sun, Dehui
Zhang, Hui
Wang, Wei
Yang, Jigang
author_sort Feng, Lijuan
collection PubMed
description OBJECTIVE: To develop and validate an (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT)-based radiomics nomogram for non-invasively prediction of bone marrow involvement (BMI) in pediatric neuroblastoma. METHODS: A total of 133 patients with neuroblastoma were retrospectively included and randomized into the training set (n = 93) and test set (n = 40). Radiomics features were extracted from both CT and PET images. The radiomics signature was developed. Independent clinical risk factors were identified using the univariate and multivariate logistic regression analyses to construct the clinical model. The clinical-radiomics model, which integrated the radiomics signature and the independent clinical risk factors, was constructed using multivariate logistic regression analysis and finally presented as a radiomics nomogram. The predictive performance of the clinical-radiomics model was evaluated by receiver operating characteristic curves, calibration curves and decision curve analysis (DCA). RESULTS: Twenty-five radiomics features were selected to construct the radiomics signature. Age at diagnosis, neuron-specific enolase and vanillylmandelic acid were identified as independent predictors to establish the clinical model. In the training set, the clinical-radiomics model outperformed the radiomics model or clinical model (AUC: 0.924 vs. 0.900, 0.875) in predicting the BMI, which was then confirmed in the test set (AUC: 0.925 vs. 0.893, 0.910). The calibration curve and DCA demonstrated that the radiomics nomogram had a good consistency and clinical utility. CONCLUSION: The (18)F-FDG PET/CT-based radiomics nomogram which incorporates radiomics signature and independent clinical risk factors could non-invasively predict BMI in pediatric neuroblastoma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13244-022-01283-8.
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spelling pubmed-94409652022-09-05 (18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma Feng, Lijuan Yang, Xu Lu, Xia Kan, Ying Wang, Chao Sun, Dehui Zhang, Hui Wang, Wei Yang, Jigang Insights Imaging Original Article OBJECTIVE: To develop and validate an (18)F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT)-based radiomics nomogram for non-invasively prediction of bone marrow involvement (BMI) in pediatric neuroblastoma. METHODS: A total of 133 patients with neuroblastoma were retrospectively included and randomized into the training set (n = 93) and test set (n = 40). Radiomics features were extracted from both CT and PET images. The radiomics signature was developed. Independent clinical risk factors were identified using the univariate and multivariate logistic regression analyses to construct the clinical model. The clinical-radiomics model, which integrated the radiomics signature and the independent clinical risk factors, was constructed using multivariate logistic regression analysis and finally presented as a radiomics nomogram. The predictive performance of the clinical-radiomics model was evaluated by receiver operating characteristic curves, calibration curves and decision curve analysis (DCA). RESULTS: Twenty-five radiomics features were selected to construct the radiomics signature. Age at diagnosis, neuron-specific enolase and vanillylmandelic acid were identified as independent predictors to establish the clinical model. In the training set, the clinical-radiomics model outperformed the radiomics model or clinical model (AUC: 0.924 vs. 0.900, 0.875) in predicting the BMI, which was then confirmed in the test set (AUC: 0.925 vs. 0.893, 0.910). The calibration curve and DCA demonstrated that the radiomics nomogram had a good consistency and clinical utility. CONCLUSION: The (18)F-FDG PET/CT-based radiomics nomogram which incorporates radiomics signature and independent clinical risk factors could non-invasively predict BMI in pediatric neuroblastoma. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13244-022-01283-8. Springer Vienna 2022-09-04 /pmc/articles/PMC9440965/ /pubmed/36057694 http://dx.doi.org/10.1186/s13244-022-01283-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Article
Feng, Lijuan
Yang, Xu
Lu, Xia
Kan, Ying
Wang, Chao
Sun, Dehui
Zhang, Hui
Wang, Wei
Yang, Jigang
(18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
title (18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
title_full (18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
title_fullStr (18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
title_full_unstemmed (18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
title_short (18)F-FDG PET/CT-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
title_sort (18)f-fdg pet/ct-based radiomics nomogram could predict bone marrow involvement in pediatric neuroblastoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440965/
https://www.ncbi.nlm.nih.gov/pubmed/36057694
http://dx.doi.org/10.1186/s13244-022-01283-8
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