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Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2
OBJECTIVES: To develop and validate a radiomics model for predicting 2019 novel coronavirus (COVID-19) pneumonia. METHODS: For this retrospective study, a radiomics model was developed on the basis of a training set consisting of 136 patients with COVID-19 pneumonia and 103 patients with other types...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332742/ https://www.ncbi.nlm.nih.gov/pubmed/32621237 http://dx.doi.org/10.1007/s00330-020-07032-z |
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author | Fang, Xu Li, Xiao Bian, Yun Ji, Xiang Lu, Jianping |
author_facet | Fang, Xu Li, Xiao Bian, Yun Ji, Xiang Lu, Jianping |
author_sort | Fang, Xu |
collection | PubMed |
description | OBJECTIVES: To develop and validate a radiomics model for predicting 2019 novel coronavirus (COVID-19) pneumonia. METHODS: For this retrospective study, a radiomics model was developed on the basis of a training set consisting of 136 patients with COVID-19 pneumonia and 103 patients with other types of viral pneumonia. Radiomics features were extracted from the lung parenchyma window. A radiomics signature was built on the basis of reproducible features, using the least absolute shrinkage and selection operator method (LASSO). Multivariable logistic regression model was adopted to establish a radiomics nomogram. Nomogram performance was determined by its discrimination, calibration, and clinical usefulness. The model was validated in 90 consecutive patients, of which 56 patients had COVID-19 pneumonia and 34 patients had other types of viral pneumonia. RESULTS: The radiomics signature, consisting of 3 selected features, was significantly associated with COVID-19 pneumonia (p < 0.05) in both training and validation sets. The multivariable logistic regression model included the radiomics signature and distribution; maximum lesion, hilar, and mediastinal lymph node enlargement; and pleural effusion. The individualized prediction nomogram showed good discrimination in the training sample (area under the receiver operating characteristic curve [AUC], 0.959; 95% confidence interval [CI], 0.933–0.985) and in the validation sample (AUC, 0.955; 95% CI, 0.899–0.995) and good calibration. The mixed model achieved better predictive efficacy than the clinical model. Decision curve analysis demonstrated that the radiomics nomogram was clinically useful. CONCLUSIONS: The radiomics model derived has good performance for predicting COVID-19 pneumonia and may help in clinical decision-making. KEY POINTS: • A radiomics model showed good performance for prediction 2019 novel coronavirus pneumonia and favorable discrimination for other types of pneumonia on CT images. • A central or peripheral distribution, a maximum lesion range > 10 cm, the involvement of all five lobes, hilar and mediastinal lymph node enlargement, and no pleural effusion is associated with an increased risk of 2019 novel coronavirus pneumonia. • A radiomics model was superior to a clinical model in predicting 2019 novel coronavirus pneumonia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-020-07032-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7332742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-73327422020-07-06 Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 Fang, Xu Li, Xiao Bian, Yun Ji, Xiang Lu, Jianping Eur Radiol Imaging Informatics and Artificial Intelligence OBJECTIVES: To develop and validate a radiomics model for predicting 2019 novel coronavirus (COVID-19) pneumonia. METHODS: For this retrospective study, a radiomics model was developed on the basis of a training set consisting of 136 patients with COVID-19 pneumonia and 103 patients with other types of viral pneumonia. Radiomics features were extracted from the lung parenchyma window. A radiomics signature was built on the basis of reproducible features, using the least absolute shrinkage and selection operator method (LASSO). Multivariable logistic regression model was adopted to establish a radiomics nomogram. Nomogram performance was determined by its discrimination, calibration, and clinical usefulness. The model was validated in 90 consecutive patients, of which 56 patients had COVID-19 pneumonia and 34 patients had other types of viral pneumonia. RESULTS: The radiomics signature, consisting of 3 selected features, was significantly associated with COVID-19 pneumonia (p < 0.05) in both training and validation sets. The multivariable logistic regression model included the radiomics signature and distribution; maximum lesion, hilar, and mediastinal lymph node enlargement; and pleural effusion. The individualized prediction nomogram showed good discrimination in the training sample (area under the receiver operating characteristic curve [AUC], 0.959; 95% confidence interval [CI], 0.933–0.985) and in the validation sample (AUC, 0.955; 95% CI, 0.899–0.995) and good calibration. The mixed model achieved better predictive efficacy than the clinical model. Decision curve analysis demonstrated that the radiomics nomogram was clinically useful. CONCLUSIONS: The radiomics model derived has good performance for predicting COVID-19 pneumonia and may help in clinical decision-making. KEY POINTS: • A radiomics model showed good performance for prediction 2019 novel coronavirus pneumonia and favorable discrimination for other types of pneumonia on CT images. • A central or peripheral distribution, a maximum lesion range > 10 cm, the involvement of all five lobes, hilar and mediastinal lymph node enlargement, and no pleural effusion is associated with an increased risk of 2019 novel coronavirus pneumonia. • A radiomics model was superior to a clinical model in predicting 2019 novel coronavirus pneumonia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-020-07032-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-07-03 2020 /pmc/articles/PMC7332742/ /pubmed/32621237 http://dx.doi.org/10.1007/s00330-020-07032-z Text en © European Society of Radiology 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Imaging Informatics and Artificial Intelligence Fang, Xu Li, Xiao Bian, Yun Ji, Xiang Lu, Jianping Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 |
title | Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 |
title_full | Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 |
title_fullStr | Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 |
title_full_unstemmed | Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 |
title_short | Radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by SARS-CoV-2 |
title_sort | radiomics nomogram for the prediction of 2019 novel coronavirus pneumonia caused by sars-cov-2 |
topic | Imaging Informatics and Artificial Intelligence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332742/ https://www.ncbi.nlm.nih.gov/pubmed/32621237 http://dx.doi.org/10.1007/s00330-020-07032-z |
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