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Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation

Objective: The stage, size, grade, and necrosis (SSIGN) score can facilitate the assessment of tumor aggressiveness and the personal management for patients with clear cell renal cell carcinoma (ccRCC). However, this score is only available after the postoperative pathological evaluation. The aim of...

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Autores principales: Jiang, Yi, Li, Wuchao, Huang, Chencui, Tian, Chong, Chen, Qi, Zeng, Xianchun, Cao, Yin, Chen, Yi, Yang, Yintong, Liu, Heng, Bo, Yonghua, Luo, Chenggong, Li, Yiming, Zhang, Tijiang, Wang, Rongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402386/
https://www.ncbi.nlm.nih.gov/pubmed/32850304
http://dx.doi.org/10.3389/fonc.2020.00909
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author Jiang, Yi
Li, Wuchao
Huang, Chencui
Tian, Chong
Chen, Qi
Zeng, Xianchun
Cao, Yin
Chen, Yi
Yang, Yintong
Liu, Heng
Bo, Yonghua
Luo, Chenggong
Li, Yiming
Zhang, Tijiang
Wang, Rongping
author_facet Jiang, Yi
Li, Wuchao
Huang, Chencui
Tian, Chong
Chen, Qi
Zeng, Xianchun
Cao, Yin
Chen, Yi
Yang, Yintong
Liu, Heng
Bo, Yonghua
Luo, Chenggong
Li, Yiming
Zhang, Tijiang
Wang, Rongping
author_sort Jiang, Yi
collection PubMed
description Objective: The stage, size, grade, and necrosis (SSIGN) score can facilitate the assessment of tumor aggressiveness and the personal management for patients with clear cell renal cell carcinoma (ccRCC). However, this score is only available after the postoperative pathological evaluation. The aim of this study was to develop and validate a CT radiomic signature for the preoperative prediction of SSIGN risk groups in patients with ccRCC in multicenters. Methods: In total, 330 patients with ccRCC from three centers were classified into the training, external validation 1, and external validation 2 cohorts. Through consistent analysis and the least absolute shrinkage and selection operator, a radiomic signature was developed to predict the SSIGN low-risk group (scores 0–3) and intermediate- to high-risk group (score ≥ 4). An image feature model was developed according to the independent image features, and a fusion model was constructed integrating the radiomic signature and the independent image features. Furthermore, the predictive performance of the above models for the SSIGN risk groups was evaluated with regard to their discrimination, calibration, and clinical usefulness. Results: A radiomic signature consisting of sixteen relevant features from the nephrographic phase CT images achieved a good calibration (all Hosmer–Lemeshow p > 0.05) and favorable prediction efficacy in the training cohort [area under the curve (AUC): 0.940, 95% confidence interval (CI): 0.884–0.973] and in the external validation cohorts (AUC: 0.876, 95% CI: 0.811–0.942; AUC: 0.928, 95% CI: 0.844–0.975, respectively). The radiomic signature performed better than the image feature model constructed by intra-tumoral vessels (all p < 0.05) and showed similar performance with the fusion model integrating radiomic signature and intra-tumoral vessels (all p > 0.05) in terms of the discrimination in all cohorts. Moreover, the decision curve analysis verified the clinical utility of the radiomic signature in both external cohorts. Conclusion: Radiomic signature could be used as a promising non-invasive tool to predict SSIGN risk groups and to facilitate preoperative clinical decision-making for patients with ccRCC.
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spelling pubmed-74023862020-08-25 Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation Jiang, Yi Li, Wuchao Huang, Chencui Tian, Chong Chen, Qi Zeng, Xianchun Cao, Yin Chen, Yi Yang, Yintong Liu, Heng Bo, Yonghua Luo, Chenggong Li, Yiming Zhang, Tijiang Wang, Rongping Front Oncol Oncology Objective: The stage, size, grade, and necrosis (SSIGN) score can facilitate the assessment of tumor aggressiveness and the personal management for patients with clear cell renal cell carcinoma (ccRCC). However, this score is only available after the postoperative pathological evaluation. The aim of this study was to develop and validate a CT radiomic signature for the preoperative prediction of SSIGN risk groups in patients with ccRCC in multicenters. Methods: In total, 330 patients with ccRCC from three centers were classified into the training, external validation 1, and external validation 2 cohorts. Through consistent analysis and the least absolute shrinkage and selection operator, a radiomic signature was developed to predict the SSIGN low-risk group (scores 0–3) and intermediate- to high-risk group (score ≥ 4). An image feature model was developed according to the independent image features, and a fusion model was constructed integrating the radiomic signature and the independent image features. Furthermore, the predictive performance of the above models for the SSIGN risk groups was evaluated with regard to their discrimination, calibration, and clinical usefulness. Results: A radiomic signature consisting of sixteen relevant features from the nephrographic phase CT images achieved a good calibration (all Hosmer–Lemeshow p > 0.05) and favorable prediction efficacy in the training cohort [area under the curve (AUC): 0.940, 95% confidence interval (CI): 0.884–0.973] and in the external validation cohorts (AUC: 0.876, 95% CI: 0.811–0.942; AUC: 0.928, 95% CI: 0.844–0.975, respectively). The radiomic signature performed better than the image feature model constructed by intra-tumoral vessels (all p < 0.05) and showed similar performance with the fusion model integrating radiomic signature and intra-tumoral vessels (all p > 0.05) in terms of the discrimination in all cohorts. Moreover, the decision curve analysis verified the clinical utility of the radiomic signature in both external cohorts. Conclusion: Radiomic signature could be used as a promising non-invasive tool to predict SSIGN risk groups and to facilitate preoperative clinical decision-making for patients with ccRCC. Frontiers Media S.A. 2020-07-28 /pmc/articles/PMC7402386/ /pubmed/32850304 http://dx.doi.org/10.3389/fonc.2020.00909 Text en Copyright © 2020 Jiang, Li, Huang, Tian, Chen, Zeng, Cao, Chen, Yang, Liu, Bo, Luo, Li, Zhang and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Jiang, Yi
Li, Wuchao
Huang, Chencui
Tian, Chong
Chen, Qi
Zeng, Xianchun
Cao, Yin
Chen, Yi
Yang, Yintong
Liu, Heng
Bo, Yonghua
Luo, Chenggong
Li, Yiming
Zhang, Tijiang
Wang, Rongping
Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation
title Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation
title_full Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation
title_fullStr Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation
title_full_unstemmed Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation
title_short Preoperative CT Radiomics Predicting the SSIGN Risk Groups in Patients With Clear Cell Renal Cell Carcinoma: Development and Multicenter Validation
title_sort preoperative ct radiomics predicting the ssign risk groups in patients with clear cell renal cell carcinoma: development and multicenter validation
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402386/
https://www.ncbi.nlm.nih.gov/pubmed/32850304
http://dx.doi.org/10.3389/fonc.2020.00909
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