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Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study
The 2019 novel coronavirus has spread rapidly around the world. Cancer patients seem to be more susceptible to infection and disease deterioration, but the factors affecting the deterioration remain unclear. We aimed to develop an individualized model for prediction of coronavirus disease (COVID‐19)...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177766/ https://www.ncbi.nlm.nih.gov/pubmed/33728806 http://dx.doi.org/10.1111/cas.14882 |
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author | Xu, Bin Song, Ke‐Han Yao, Yi Dong, Xiao‐Rong Li, Lin‐Jun Wang, Qun Yang, Ji‐Yuan Hu, Wei‐Dong Xie, Zhi‐Bin Luo, Zhi‐Guo Luo, Xiu‐Li Liu, Jing Rao, Zhi‐Guo Zhang, Hui‐Bo Wu, Jie Li, Lan Gong, Hong‐Yun Chu, Qian Song, Qi‐Bin Wang, Jie |
author_facet | Xu, Bin Song, Ke‐Han Yao, Yi Dong, Xiao‐Rong Li, Lin‐Jun Wang, Qun Yang, Ji‐Yuan Hu, Wei‐Dong Xie, Zhi‐Bin Luo, Zhi‐Guo Luo, Xiu‐Li Liu, Jing Rao, Zhi‐Guo Zhang, Hui‐Bo Wu, Jie Li, Lan Gong, Hong‐Yun Chu, Qian Song, Qi‐Bin Wang, Jie |
author_sort | Xu, Bin |
collection | PubMed |
description | The 2019 novel coronavirus has spread rapidly around the world. Cancer patients seem to be more susceptible to infection and disease deterioration, but the factors affecting the deterioration remain unclear. We aimed to develop an individualized model for prediction of coronavirus disease (COVID‐19) deterioration in cancer patients. The clinical data of 276 cancer patients diagnosed with COVID‐19 in 33 designated hospitals of Hubei, China from December 21, 2019 to March 18, 2020, were collected and randomly divided into a training and a validation cohort by a ratio of 2:1. Cox stepwise regression analysis was carried out to select prognostic factors. The prediction model was developed in the training cohort. The predictive accuracy of the model was quantified by C‐index and time‐dependent area under the receiver operating characteristic curve (t‐AUC). Internal validation was assessed by the validation cohort. Risk stratification based on the model was carried out. Decision curve analysis (DCA) were used to evaluate the clinical usefulness of the model. We found age, cancer type, computed tomography baseline image features (ground glass opacity and consolidation), laboratory findings (lymphocyte count, serum levels of C‐reactive protein, aspartate aminotransferase, direct bilirubin, urea, and d‐dimer) were significantly associated with symptomatic deterioration. The C‐index of the model was 0.755 in the training cohort and 0.779 in the validation cohort. The t‐AUC values were above 0.7 within 8 weeks both in the training and validation cohorts. Patients were divided into two risk groups based on the nomogram: low‐risk (total points ≤ 9.98) and high‐risk (total points > 9.98) group. The Kaplan‐Meier deterioration‐free survival of COVID‐19 curves presented significant discrimination between the two risk groups in both training and validation cohorts. The model indicated good clinical applicability by DCA curves. This study presents an individualized nomogram model to individually predict the possibility of symptomatic deterioration of COVID‐19 in patients with cancer. |
format | Online Article Text |
id | pubmed-8177766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81777662021-06-15 Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study Xu, Bin Song, Ke‐Han Yao, Yi Dong, Xiao‐Rong Li, Lin‐Jun Wang, Qun Yang, Ji‐Yuan Hu, Wei‐Dong Xie, Zhi‐Bin Luo, Zhi‐Guo Luo, Xiu‐Li Liu, Jing Rao, Zhi‐Guo Zhang, Hui‐Bo Wu, Jie Li, Lan Gong, Hong‐Yun Chu, Qian Song, Qi‐Bin Wang, Jie Cancer Sci Original Articles The 2019 novel coronavirus has spread rapidly around the world. Cancer patients seem to be more susceptible to infection and disease deterioration, but the factors affecting the deterioration remain unclear. We aimed to develop an individualized model for prediction of coronavirus disease (COVID‐19) deterioration in cancer patients. The clinical data of 276 cancer patients diagnosed with COVID‐19 in 33 designated hospitals of Hubei, China from December 21, 2019 to March 18, 2020, were collected and randomly divided into a training and a validation cohort by a ratio of 2:1. Cox stepwise regression analysis was carried out to select prognostic factors. The prediction model was developed in the training cohort. The predictive accuracy of the model was quantified by C‐index and time‐dependent area under the receiver operating characteristic curve (t‐AUC). Internal validation was assessed by the validation cohort. Risk stratification based on the model was carried out. Decision curve analysis (DCA) were used to evaluate the clinical usefulness of the model. We found age, cancer type, computed tomography baseline image features (ground glass opacity and consolidation), laboratory findings (lymphocyte count, serum levels of C‐reactive protein, aspartate aminotransferase, direct bilirubin, urea, and d‐dimer) were significantly associated with symptomatic deterioration. The C‐index of the model was 0.755 in the training cohort and 0.779 in the validation cohort. The t‐AUC values were above 0.7 within 8 weeks both in the training and validation cohorts. Patients were divided into two risk groups based on the nomogram: low‐risk (total points ≤ 9.98) and high‐risk (total points > 9.98) group. The Kaplan‐Meier deterioration‐free survival of COVID‐19 curves presented significant discrimination between the two risk groups in both training and validation cohorts. The model indicated good clinical applicability by DCA curves. This study presents an individualized nomogram model to individually predict the possibility of symptomatic deterioration of COVID‐19 in patients with cancer. John Wiley and Sons Inc. 2021-05-01 2021-06 /pmc/articles/PMC8177766/ /pubmed/33728806 http://dx.doi.org/10.1111/cas.14882 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Xu, Bin Song, Ke‐Han Yao, Yi Dong, Xiao‐Rong Li, Lin‐Jun Wang, Qun Yang, Ji‐Yuan Hu, Wei‐Dong Xie, Zhi‐Bin Luo, Zhi‐Guo Luo, Xiu‐Li Liu, Jing Rao, Zhi‐Guo Zhang, Hui‐Bo Wu, Jie Li, Lan Gong, Hong‐Yun Chu, Qian Song, Qi‐Bin Wang, Jie Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study |
title | Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study |
title_full | Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study |
title_fullStr | Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study |
title_full_unstemmed | Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study |
title_short | Individualized model for predicting COVID‐19 deterioration in patients with cancer: A multicenter retrospective study |
title_sort | individualized model for predicting covid‐19 deterioration in patients with cancer: a multicenter retrospective study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177766/ https://www.ncbi.nlm.nih.gov/pubmed/33728806 http://dx.doi.org/10.1111/cas.14882 |
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