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Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma

BACKGROUND: Heterogeneity of metastatic renal cell carcinoma (RCC) constraints accurate prognosis prediction of the tumor. We therefore aimed at developing a novel nomogram for accurate prediction of overall survival (OS) of patients with metastatic RCC. METHODS: We extracted 2010 to 2016 data for m...

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Autores principales: Zheng, Wenwen, Zhu, Weiwei, Yu, Shengqiang, Li, Kangqi, Ding, Yuexia, Wu, Qingna, Tang, Qiling, Zhao, Quan, Lu, Congxiao, Guo, Chenyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640685/
https://www.ncbi.nlm.nih.gov/pubmed/33148204
http://dx.doi.org/10.1186/s12885-020-07586-7
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author Zheng, Wenwen
Zhu, Weiwei
Yu, Shengqiang
Li, Kangqi
Ding, Yuexia
Wu, Qingna
Tang, Qiling
Zhao, Quan
Lu, Congxiao
Guo, Chenyu
author_facet Zheng, Wenwen
Zhu, Weiwei
Yu, Shengqiang
Li, Kangqi
Ding, Yuexia
Wu, Qingna
Tang, Qiling
Zhao, Quan
Lu, Congxiao
Guo, Chenyu
author_sort Zheng, Wenwen
collection PubMed
description BACKGROUND: Heterogeneity of metastatic renal cell carcinoma (RCC) constraints accurate prognosis prediction of the tumor. We therefore aimed at developing a novel nomogram for accurate prediction of overall survival (OS) of patients with metastatic RCC. METHODS: We extracted 2010 to 2016 data for metastatic RCC patients in the Surveillance, Epidemiology, and End Results (SEER) database, and randomly stratified them equally into training and validation sets. Prognostic factors for OS were analyzed using Cox regression models, and thereafter integrated into a 1, 3 and 5-year OS predictive nomogram. The nomogram was validated using the training and validation sets. The performance of this model was evaluated by the Harrell’s concordance index (C-index), calibration curve, integrated discrimination improvement (IDI), category-free net reclassification improvement (NRI), index of prediction accuracy (IPA), and decision curve analysis (DCA). RESULTS: Overall, 2315 metastatic RCC patients in the SEER database who fulfilled our inclusion criteria were utilized in constructing a nomogram for predicting OS of newly diagnosed metastatic RCC patients. The nomogram incorporated eight clinical factors: Fuhrman grade, lymph node status, sarcomatoid feature, cancer-directed surgery and bone, brain, liver, and lung metastases, all significantly associated with OS. The model was superior to the American Joint Committee on Cancer (AJCC) staging system (7th edition) both in training (C-indices, 0.701 vs. 0.612, P < 0.001) and validation sets (C-indices, 0.676 vs. 0.600, P < 0.001). The calibration plots of the nomogram corresponded well between predicted and observed values. NRI, IDI, and IPA further validated the superior predictive capability of the nomogram relative to the AJCC staging system. The DCA plots revealed reliable clinical application of our model in prognosis prediction of metastatic RCC patients. CONCLUSIONS: We developed and validated an accurate nomogram for individual OS prediction of metastatic RCC patients. This nomogram can be applied in design of clinical trials, patient counseling, and rationalizing therapeutic modalities.
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spelling pubmed-76406852020-11-04 Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma Zheng, Wenwen Zhu, Weiwei Yu, Shengqiang Li, Kangqi Ding, Yuexia Wu, Qingna Tang, Qiling Zhao, Quan Lu, Congxiao Guo, Chenyu BMC Cancer Research Article BACKGROUND: Heterogeneity of metastatic renal cell carcinoma (RCC) constraints accurate prognosis prediction of the tumor. We therefore aimed at developing a novel nomogram for accurate prediction of overall survival (OS) of patients with metastatic RCC. METHODS: We extracted 2010 to 2016 data for metastatic RCC patients in the Surveillance, Epidemiology, and End Results (SEER) database, and randomly stratified them equally into training and validation sets. Prognostic factors for OS were analyzed using Cox regression models, and thereafter integrated into a 1, 3 and 5-year OS predictive nomogram. The nomogram was validated using the training and validation sets. The performance of this model was evaluated by the Harrell’s concordance index (C-index), calibration curve, integrated discrimination improvement (IDI), category-free net reclassification improvement (NRI), index of prediction accuracy (IPA), and decision curve analysis (DCA). RESULTS: Overall, 2315 metastatic RCC patients in the SEER database who fulfilled our inclusion criteria were utilized in constructing a nomogram for predicting OS of newly diagnosed metastatic RCC patients. The nomogram incorporated eight clinical factors: Fuhrman grade, lymph node status, sarcomatoid feature, cancer-directed surgery and bone, brain, liver, and lung metastases, all significantly associated with OS. The model was superior to the American Joint Committee on Cancer (AJCC) staging system (7th edition) both in training (C-indices, 0.701 vs. 0.612, P < 0.001) and validation sets (C-indices, 0.676 vs. 0.600, P < 0.001). The calibration plots of the nomogram corresponded well between predicted and observed values. NRI, IDI, and IPA further validated the superior predictive capability of the nomogram relative to the AJCC staging system. The DCA plots revealed reliable clinical application of our model in prognosis prediction of metastatic RCC patients. CONCLUSIONS: We developed and validated an accurate nomogram for individual OS prediction of metastatic RCC patients. This nomogram can be applied in design of clinical trials, patient counseling, and rationalizing therapeutic modalities. BioMed Central 2020-11-04 /pmc/articles/PMC7640685/ /pubmed/33148204 http://dx.doi.org/10.1186/s12885-020-07586-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Zheng, Wenwen
Zhu, Weiwei
Yu, Shengqiang
Li, Kangqi
Ding, Yuexia
Wu, Qingna
Tang, Qiling
Zhao, Quan
Lu, Congxiao
Guo, Chenyu
Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
title Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
title_full Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
title_fullStr Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
title_full_unstemmed Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
title_short Development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
title_sort development and validation of a nomogram to predict overall survival for patients with metastatic renal cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7640685/
https://www.ncbi.nlm.nih.gov/pubmed/33148204
http://dx.doi.org/10.1186/s12885-020-07586-7
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