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Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer
Accurate identification of patients with poor prognosis after radical surgery is essential for clinical management of colon cancer. Thus, we aimed to develop death and relapse specific radiomics signatures to individually estimate overall survival (OS) and relapse free survival (RFS) of colon cancer...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240849/ https://www.ncbi.nlm.nih.gov/pubmed/32508036 http://dx.doi.org/10.1002/ctm2.31 |
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author | Dai, Weixing Mo, Shaobo Han, Lingyu Xiang, Wenqiang Li, Menglei Wang, Renjie Tong, Tong Cai, Guoxiang |
author_facet | Dai, Weixing Mo, Shaobo Han, Lingyu Xiang, Wenqiang Li, Menglei Wang, Renjie Tong, Tong Cai, Guoxiang |
author_sort | Dai, Weixing |
collection | PubMed |
description | Accurate identification of patients with poor prognosis after radical surgery is essential for clinical management of colon cancer. Thus, we aimed to develop death and relapse specific radiomics signatures to individually estimate overall survival (OS) and relapse free survival (RFS) of colon cancer patients. In this study, 701 stage I‐III colon cancer patients were identified from Fudan University Shanghai Cancer Center. A total of 647 three‐dimensional features were extracted from computed tomography images. LASSO Cox was used to identify the significantly death‐ and relapse‐associated features and to build death and relapse specific radiomics signatures, respectively. A total of 13 death‐specific and 26 relapse‐specific features were identified from 647 screened radiomics features. The developed signatures can divide patients into two groups with significantly different death (Hazard Ratio (HR): 3.053; 95% CI, 1.78‐5.23; P < .001) or relapse risk (HR: 2.794; 95% CI, 1.87‐4.16; P < .001). Time‐dependent Relative operating characteristic curve showed that the signatures performed better than any other clinicopathological factors in predicting OS (AUC: 0.768; 95% CI, 0.745‐0.791) and RFS (AUC: 0.744; 95% CI, 0.687‐0.801). Further, survival decision curve analyses confirmed the good clinical utility of the two radiomics signatures. In conclusion, we successfully developed death‐ and relapse‐specific radiomics signatures that can accurately predict OS and RFS, which may facilitate personalized treatment. |
format | Online Article Text |
id | pubmed-7240849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72408492020-06-01 Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer Dai, Weixing Mo, Shaobo Han, Lingyu Xiang, Wenqiang Li, Menglei Wang, Renjie Tong, Tong Cai, Guoxiang Clin Transl Med Short Communication Accurate identification of patients with poor prognosis after radical surgery is essential for clinical management of colon cancer. Thus, we aimed to develop death and relapse specific radiomics signatures to individually estimate overall survival (OS) and relapse free survival (RFS) of colon cancer patients. In this study, 701 stage I‐III colon cancer patients were identified from Fudan University Shanghai Cancer Center. A total of 647 three‐dimensional features were extracted from computed tomography images. LASSO Cox was used to identify the significantly death‐ and relapse‐associated features and to build death and relapse specific radiomics signatures, respectively. A total of 13 death‐specific and 26 relapse‐specific features were identified from 647 screened radiomics features. The developed signatures can divide patients into two groups with significantly different death (Hazard Ratio (HR): 3.053; 95% CI, 1.78‐5.23; P < .001) or relapse risk (HR: 2.794; 95% CI, 1.87‐4.16; P < .001). Time‐dependent Relative operating characteristic curve showed that the signatures performed better than any other clinicopathological factors in predicting OS (AUC: 0.768; 95% CI, 0.745‐0.791) and RFS (AUC: 0.744; 95% CI, 0.687‐0.801). Further, survival decision curve analyses confirmed the good clinical utility of the two radiomics signatures. In conclusion, we successfully developed death‐ and relapse‐specific radiomics signatures that can accurately predict OS and RFS, which may facilitate personalized treatment. John Wiley and Sons Inc. 2020-04-30 /pmc/articles/PMC7240849/ /pubmed/32508036 http://dx.doi.org/10.1002/ctm2.31 Text en © 2020 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Dai, Weixing Mo, Shaobo Han, Lingyu Xiang, Wenqiang Li, Menglei Wang, Renjie Tong, Tong Cai, Guoxiang Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer |
title | Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer |
title_full | Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer |
title_fullStr | Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer |
title_full_unstemmed | Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer |
title_short | Prognostic and predictive value of radiomics signatures in stage I‐III colon cancer |
title_sort | prognostic and predictive value of radiomics signatures in stage i‐iii colon cancer |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240849/ https://www.ncbi.nlm.nih.gov/pubmed/32508036 http://dx.doi.org/10.1002/ctm2.31 |
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