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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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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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. |
format | Online Article Text |
id | pubmed-4823134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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