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Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival

The aim of this study was to develop a prognostic classifier and subdivided the M1 stage for nasopharyngeal carcinoma patients with synchronous metastases (mNPC). A retrospective cohort of 347 mNPC patients was recruited between January 2000 and December 2010. Thirty hematological markers and 11 cli...

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Autores principales: Jiang, Rou, You, Rui, Pei, Xiao-Qing, Zou, Xiong, Zhang, Meng-Xia, Wang, Tong-Min, Sun, Rui, Luo, Dong-Hua, Huang, Pei-Yu, Chen, Qiu-Yan, Hua, Yi-Jun, Tang, Lin-Quan, Guo, Ling, Mo, Hao-Yuan, Qian, Chao-Nan, Mai, Hai-Qiang, Hong, Ming-Huang, Cai, Hong-Min, Chen, Ming-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823134/
https://www.ncbi.nlm.nih.gov/pubmed/26636646
http://dx.doi.org/10.18632/oncotarget.6436
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author Jiang, Rou
You, Rui
Pei, Xiao-Qing
Zou, Xiong
Zhang, Meng-Xia
Wang, Tong-Min
Sun, Rui
Luo, Dong-Hua
Huang, Pei-Yu
Chen, Qiu-Yan
Hua, Yi-Jun
Tang, Lin-Quan
Guo, Ling
Mo, Hao-Yuan
Qian, Chao-Nan
Mai, Hai-Qiang
Hong, Ming-Huang
Cai, Hong-Min
Chen, Ming-Yuan
author_facet Jiang, Rou
You, Rui
Pei, Xiao-Qing
Zou, Xiong
Zhang, Meng-Xia
Wang, Tong-Min
Sun, Rui
Luo, Dong-Hua
Huang, Pei-Yu
Chen, Qiu-Yan
Hua, Yi-Jun
Tang, Lin-Quan
Guo, Ling
Mo, Hao-Yuan
Qian, Chao-Nan
Mai, Hai-Qiang
Hong, Ming-Huang
Cai, Hong-Min
Chen, Ming-Yuan
author_sort Jiang, Rou
collection PubMed
description The aim of this study was to develop a prognostic classifier and subdivided the M1 stage for nasopharyngeal carcinoma patients with synchronous metastases (mNPC). A retrospective cohort of 347 mNPC patients was recruited between January 2000 and December 2010. Thirty hematological markers and 11 clinical characteristics were collected, and the association of these factors with overall survival (OS) was evaluated. Advanced machine learning schemes of a support vector machine (SVM) were used to select a subset of highly informative factors and to construct a prognostic model (mNPC-SVM). The mNPC-SVM classifier identified ten informative variables, including three clinical indexes and seven hematological markers. The median survival time for low-risk patients (M1a) as identified by the mNPC-SVM classifier was 38.0 months, and survival time was dramatically reduced to 13.8 months for high-risk patients (M1b) (P < 0.001). Multivariate adjustment using prognostic factors revealed that the mNPC-SVM classifier remained a powerful predictor of OS (M1a vs. M1b, hazard ratio, 3.45; 95% CI, 2.59 to 4.60, P < 0.001). Moreover, combination treatment of systemic chemotherapy and loco-regional radiotherapy was associated with significantly better survival outcomes than chemotherapy alone (the 5-year OS, 47.0% vs. 10.0%, P < 0.001) in the M1a subgroup but not in the M1b subgroup (12.0% vs. 3.0%, P = 0.101). These findings were validated by a separate cohort. In conclusion, the newly developed mNPC-SVM classifier led to more precise risk definitions that offer a promising subdivision of the M1 stage and individualized selection for future therapeutic regimens in mNPC patients.
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spelling pubmed-48231342016-05-03 Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival Jiang, Rou You, Rui Pei, Xiao-Qing Zou, Xiong Zhang, Meng-Xia Wang, Tong-Min Sun, Rui Luo, Dong-Hua Huang, Pei-Yu Chen, Qiu-Yan Hua, Yi-Jun Tang, Lin-Quan Guo, Ling Mo, Hao-Yuan Qian, Chao-Nan Mai, Hai-Qiang Hong, Ming-Huang Cai, Hong-Min Chen, Ming-Yuan Oncotarget Clinical Research Paper The aim of this study was to develop a prognostic classifier and subdivided the M1 stage for nasopharyngeal carcinoma patients with synchronous metastases (mNPC). A retrospective cohort of 347 mNPC patients was recruited between January 2000 and December 2010. Thirty hematological markers and 11 clinical characteristics were collected, and the association of these factors with overall survival (OS) was evaluated. Advanced machine learning schemes of a support vector machine (SVM) were used to select a subset of highly informative factors and to construct a prognostic model (mNPC-SVM). The mNPC-SVM classifier identified ten informative variables, including three clinical indexes and seven hematological markers. The median survival time for low-risk patients (M1a) as identified by the mNPC-SVM classifier was 38.0 months, and survival time was dramatically reduced to 13.8 months for high-risk patients (M1b) (P < 0.001). Multivariate adjustment using prognostic factors revealed that the mNPC-SVM classifier remained a powerful predictor of OS (M1a vs. M1b, hazard ratio, 3.45; 95% CI, 2.59 to 4.60, P < 0.001). Moreover, combination treatment of systemic chemotherapy and loco-regional radiotherapy was associated with significantly better survival outcomes than chemotherapy alone (the 5-year OS, 47.0% vs. 10.0%, P < 0.001) in the M1a subgroup but not in the M1b subgroup (12.0% vs. 3.0%, P = 0.101). These findings were validated by a separate cohort. In conclusion, the newly developed mNPC-SVM classifier led to more precise risk definitions that offer a promising subdivision of the M1 stage and individualized selection for future therapeutic regimens in mNPC patients. Impact Journals LLC 2015-11-30 /pmc/articles/PMC4823134/ /pubmed/26636646 http://dx.doi.org/10.18632/oncotarget.6436 Text en Copyright: © 2016 Jiang et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Jiang, Rou
You, Rui
Pei, Xiao-Qing
Zou, Xiong
Zhang, Meng-Xia
Wang, Tong-Min
Sun, Rui
Luo, Dong-Hua
Huang, Pei-Yu
Chen, Qiu-Yan
Hua, Yi-Jun
Tang, Lin-Quan
Guo, Ling
Mo, Hao-Yuan
Qian, Chao-Nan
Mai, Hai-Qiang
Hong, Ming-Huang
Cai, Hong-Min
Chen, Ming-Yuan
Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
title Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
title_full Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
title_fullStr Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
title_full_unstemmed Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
title_short Development of a ten-signature classifier using a support vector machine integrated approach to subdivide the M1 stage into M1a and M1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
title_sort development of a ten-signature classifier using a support vector machine integrated approach to subdivide the m1 stage into m1a and m1b stages of nasopharyngeal carcinoma with synchronous metastases to better predict patients' survival
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823134/
https://www.ncbi.nlm.nih.gov/pubmed/26636646
http://dx.doi.org/10.18632/oncotarget.6436
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