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Nomogram application to predict overall and cancer-specific survival in osteosarcoma
PURPOSE: A prognostic nomogram was applied to predict survival in osteosarcoma patients. PATIENTS AND METHODS: Data collected from 2,195 osteosarcoma patients in the Surveillance, Epidemiology, and End Results (SEER) database between 1983 and 2014 were analyzed. Independent prognostic factors were i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235004/ https://www.ncbi.nlm.nih.gov/pubmed/30519092 http://dx.doi.org/10.2147/CMAR.S177945 |
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author | Zheng, Weipeng Huang, Yuanping Chen, Haoyi Wang, Ning Xiao, Wende Liang, YingJie Jiang, Xin Su, Wenzhou Wen, Shifeng |
author_facet | Zheng, Weipeng Huang, Yuanping Chen, Haoyi Wang, Ning Xiao, Wende Liang, YingJie Jiang, Xin Su, Wenzhou Wen, Shifeng |
author_sort | Zheng, Weipeng |
collection | PubMed |
description | PURPOSE: A prognostic nomogram was applied to predict survival in osteosarcoma patients. PATIENTS AND METHODS: Data collected from 2,195 osteosarcoma patients in the Surveillance, Epidemiology, and End Results (SEER) database between 1983 and 2014 were analyzed. Independent prognostic factors were identified via univariate and multivariate Cox analyses. These were incorporated into a nomogram to predict 3- and 5-year overall survival (OS) and cancer-specific survival (CSS) rates. Internal and external data were used for validation. Concordance indices (C-indices) were used to estimate nomogram accuracy. RESULTS: Patients were randomly assigned into a training cohort (n=1,098) or validation cohort (n=1,097). Age at diagnosis, tumor site, histology, tumor size, tumor stage, use of surgery, and tumor grade were identified as independent prognostic factors via univariate and multivariate Cox analyses (all P<0.05) and then included in the prognostic nomogram. C-indices for OS and CSS prediction in the training cohort were 0.763 (95% CI 0.761–0.764) and 0.764 (95% CI 0.762–0.765), respectively. C-indices for OS and CSS prediction in the external validation cohort were 0.739 (95% CI 0.737–0.740) and 0.740 (95% CI, 0.738–0.741), respectively. Calibration plots revealed excellent consistency between actual survival and nomogram prediction. CONCLUSION: Nomograms were constructed to predict OS and CSS for osteosarcoma patients in the SEER database. They provide accurate and individualized survival prediction. |
format | Online Article Text |
id | pubmed-6235004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62350042018-12-05 Nomogram application to predict overall and cancer-specific survival in osteosarcoma Zheng, Weipeng Huang, Yuanping Chen, Haoyi Wang, Ning Xiao, Wende Liang, YingJie Jiang, Xin Su, Wenzhou Wen, Shifeng Cancer Manag Res Original Research PURPOSE: A prognostic nomogram was applied to predict survival in osteosarcoma patients. PATIENTS AND METHODS: Data collected from 2,195 osteosarcoma patients in the Surveillance, Epidemiology, and End Results (SEER) database between 1983 and 2014 were analyzed. Independent prognostic factors were identified via univariate and multivariate Cox analyses. These were incorporated into a nomogram to predict 3- and 5-year overall survival (OS) and cancer-specific survival (CSS) rates. Internal and external data were used for validation. Concordance indices (C-indices) were used to estimate nomogram accuracy. RESULTS: Patients were randomly assigned into a training cohort (n=1,098) or validation cohort (n=1,097). Age at diagnosis, tumor site, histology, tumor size, tumor stage, use of surgery, and tumor grade were identified as independent prognostic factors via univariate and multivariate Cox analyses (all P<0.05) and then included in the prognostic nomogram. C-indices for OS and CSS prediction in the training cohort were 0.763 (95% CI 0.761–0.764) and 0.764 (95% CI 0.762–0.765), respectively. C-indices for OS and CSS prediction in the external validation cohort were 0.739 (95% CI 0.737–0.740) and 0.740 (95% CI, 0.738–0.741), respectively. Calibration plots revealed excellent consistency between actual survival and nomogram prediction. CONCLUSION: Nomograms were constructed to predict OS and CSS for osteosarcoma patients in the SEER database. They provide accurate and individualized survival prediction. Dove Medical Press 2018-11-08 /pmc/articles/PMC6235004/ /pubmed/30519092 http://dx.doi.org/10.2147/CMAR.S177945 Text en © 2018 Zheng et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zheng, Weipeng Huang, Yuanping Chen, Haoyi Wang, Ning Xiao, Wende Liang, YingJie Jiang, Xin Su, Wenzhou Wen, Shifeng Nomogram application to predict overall and cancer-specific survival in osteosarcoma |
title | Nomogram application to predict overall and cancer-specific survival in osteosarcoma |
title_full | Nomogram application to predict overall and cancer-specific survival in osteosarcoma |
title_fullStr | Nomogram application to predict overall and cancer-specific survival in osteosarcoma |
title_full_unstemmed | Nomogram application to predict overall and cancer-specific survival in osteosarcoma |
title_short | Nomogram application to predict overall and cancer-specific survival in osteosarcoma |
title_sort | nomogram application to predict overall and cancer-specific survival in osteosarcoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6235004/ https://www.ncbi.nlm.nih.gov/pubmed/30519092 http://dx.doi.org/10.2147/CMAR.S177945 |
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