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A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter
Background: To establish a prognostic score based on clinical routine factors to stratify nasopharyngeal carcinoma patients with bone metastasis into risk groups with different survival rates. Materials and Methods: Total 276 patients from multicenter were retrospectively analyzed. Kaplan-Meier meth...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868144/ https://www.ncbi.nlm.nih.gov/pubmed/29581758 http://dx.doi.org/10.7150/jca.22663 |
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author | Chen, Chen Wu, Jing-Bo Jiang, Hao Gao, Jin Chen, Jia-Xin Pan, Chang-Chuan Shen, Lu-Jun Chen, Yu Chang, Hui Tao, Ya-Lan Li, Xiao-Hui Wu, Pei-Hong Xia, Yun-Fei |
author_facet | Chen, Chen Wu, Jing-Bo Jiang, Hao Gao, Jin Chen, Jia-Xin Pan, Chang-Chuan Shen, Lu-Jun Chen, Yu Chang, Hui Tao, Ya-Lan Li, Xiao-Hui Wu, Pei-Hong Xia, Yun-Fei |
author_sort | Chen, Chen |
collection | PubMed |
description | Background: To establish a prognostic score based on clinical routine factors to stratify nasopharyngeal carcinoma patients with bone metastasis into risk groups with different survival rates. Materials and Methods: Total 276 patients from multicenter were retrospectively analyzed. Kaplan-Meier method and Cox regression were used to confirm independent risk factors, which were checked for internal validity by bootstrapping method. The prognostic score, deriving from the corresponding regression coefficients in Cox model, classified patients into low and high risk groups. Finally, two independent cohorts were used for external validation. Results: In development cohort, six risk factors were identified: age>46 year-old (point=1), N>0 stage (point=2), anemia (point=2), bone metastasis free interval≤12 months (point=1), without radiotherapy to primary sites (point=1), and without radiotherapy to first metastasis sites (point=1). The derived prognostic score divided patients into low (score, 0-4) and high (score, 5-8) risk groups, with highly significant differences of 5-year overall survival rates (high vs. low risk: 24.6% vs. 58.2%, HR 3.47, P<0.001). Two external validations presented congruent results. Conclusion: A feasible and applicative prognostic score was successfully established and validated to discriminate bone metastatic nasopharyngeal carcinoma into low/high risk groups, which will be useful for individual treatment. |
format | Online Article Text |
id | pubmed-5868144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-58681442018-03-26 A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter Chen, Chen Wu, Jing-Bo Jiang, Hao Gao, Jin Chen, Jia-Xin Pan, Chang-Chuan Shen, Lu-Jun Chen, Yu Chang, Hui Tao, Ya-Lan Li, Xiao-Hui Wu, Pei-Hong Xia, Yun-Fei J Cancer Research Paper Background: To establish a prognostic score based on clinical routine factors to stratify nasopharyngeal carcinoma patients with bone metastasis into risk groups with different survival rates. Materials and Methods: Total 276 patients from multicenter were retrospectively analyzed. Kaplan-Meier method and Cox regression were used to confirm independent risk factors, which were checked for internal validity by bootstrapping method. The prognostic score, deriving from the corresponding regression coefficients in Cox model, classified patients into low and high risk groups. Finally, two independent cohorts were used for external validation. Results: In development cohort, six risk factors were identified: age>46 year-old (point=1), N>0 stage (point=2), anemia (point=2), bone metastasis free interval≤12 months (point=1), without radiotherapy to primary sites (point=1), and without radiotherapy to first metastasis sites (point=1). The derived prognostic score divided patients into low (score, 0-4) and high (score, 5-8) risk groups, with highly significant differences of 5-year overall survival rates (high vs. low risk: 24.6% vs. 58.2%, HR 3.47, P<0.001). Two external validations presented congruent results. Conclusion: A feasible and applicative prognostic score was successfully established and validated to discriminate bone metastatic nasopharyngeal carcinoma into low/high risk groups, which will be useful for individual treatment. Ivyspring International Publisher 2018-02-12 /pmc/articles/PMC5868144/ /pubmed/29581758 http://dx.doi.org/10.7150/jca.22663 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Chen, Chen Wu, Jing-Bo Jiang, Hao Gao, Jin Chen, Jia-Xin Pan, Chang-Chuan Shen, Lu-Jun Chen, Yu Chang, Hui Tao, Ya-Lan Li, Xiao-Hui Wu, Pei-Hong Xia, Yun-Fei A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter |
title | A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter |
title_full | A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter |
title_fullStr | A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter |
title_full_unstemmed | A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter |
title_short | A Prognostic Score for Nasopharyngeal Carcinoma with Bone Metastasis: Development and Validation from Multicenter |
title_sort | prognostic score for nasopharyngeal carcinoma with bone metastasis: development and validation from multicenter |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868144/ https://www.ncbi.nlm.nih.gov/pubmed/29581758 http://dx.doi.org/10.7150/jca.22663 |
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