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Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma

BACKGROUND: We aim to develop effective models for predicting postoperative distant metastasis for oesophageal squamous cell carcinoma (OSCC) for the purpose of guiding tailored therapy. METHODS: We used data from two centres to establish training (n=319) and validation (n=164) cohorts. All patients...

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Autores principales: Yang, H X, Feng, W, Wei, J C, Zeng, T S, Li, Z D, Zhang, L J, Lin, P, Luo, R Z, He, J H, Fu, J H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778272/
https://www.ncbi.nlm.nih.gov/pubmed/23942069
http://dx.doi.org/10.1038/bjc.2013.379
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author Yang, H X
Feng, W
Wei, J C
Zeng, T S
Li, Z D
Zhang, L J
Lin, P
Luo, R Z
He, J H
Fu, J H
author_facet Yang, H X
Feng, W
Wei, J C
Zeng, T S
Li, Z D
Zhang, L J
Lin, P
Luo, R Z
He, J H
Fu, J H
author_sort Yang, H X
collection PubMed
description BACKGROUND: We aim to develop effective models for predicting postoperative distant metastasis for oesophageal squamous cell carcinoma (OSCC) for the purpose of guiding tailored therapy. METHODS: We used data from two centres to establish training (n=319) and validation (n=164) cohorts. All patients underwent curative surgical treatment. The clinicopathological features and 23 immunomarkers detected by immunohistochemistry were involved for variable selection. We constructed eight support vector machine (SVM)-based nomograms (SVM1–SVM4 and SVM1'–SVM4'). The nomogram constructed with the training cohort was tested further with the validation cohort. RESULTS: The outcome of the SVM1 model in predicting postoperative distant metastasis was as follows: sensitivity, 44.7% specificity, 90.9% positive predictive value, 81.0% negative predictive value, 65.6% and overall accuracy, 69.5%. The corresponding outcome of the SVM2 model was as follows: 44.7%, 92.1%, 82.9%, 65.9%, and 70.1%, respectively. The corresponding outcome of the SVM3 model was as follows: 55.3%, 93.2%, 87.5%, 70.7%, and 75.6%, respectively. The SVM4 model was the most effective nomogram in prediction, and the corresponding outcome was as follows: 56.6%, 97.7%, 95.6%, 72.3%, and 78.7%, respectively.Similar results were observed in SVM1', SVM2', SVM3', and SVM4', respectively. CONCLUSION: The SVM-based models integrating clinicopathological features and molecular markers as variables are helpful in selecting the patients of OSCC with high risk of postoperative distant metastasis.
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spelling pubmed-37782722014-09-03 Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma Yang, H X Feng, W Wei, J C Zeng, T S Li, Z D Zhang, L J Lin, P Luo, R Z He, J H Fu, J H Br J Cancer Clinical Study BACKGROUND: We aim to develop effective models for predicting postoperative distant metastasis for oesophageal squamous cell carcinoma (OSCC) for the purpose of guiding tailored therapy. METHODS: We used data from two centres to establish training (n=319) and validation (n=164) cohorts. All patients underwent curative surgical treatment. The clinicopathological features and 23 immunomarkers detected by immunohistochemistry were involved for variable selection. We constructed eight support vector machine (SVM)-based nomograms (SVM1–SVM4 and SVM1'–SVM4'). The nomogram constructed with the training cohort was tested further with the validation cohort. RESULTS: The outcome of the SVM1 model in predicting postoperative distant metastasis was as follows: sensitivity, 44.7% specificity, 90.9% positive predictive value, 81.0% negative predictive value, 65.6% and overall accuracy, 69.5%. The corresponding outcome of the SVM2 model was as follows: 44.7%, 92.1%, 82.9%, 65.9%, and 70.1%, respectively. The corresponding outcome of the SVM3 model was as follows: 55.3%, 93.2%, 87.5%, 70.7%, and 75.6%, respectively. The SVM4 model was the most effective nomogram in prediction, and the corresponding outcome was as follows: 56.6%, 97.7%, 95.6%, 72.3%, and 78.7%, respectively.Similar results were observed in SVM1', SVM2', SVM3', and SVM4', respectively. CONCLUSION: The SVM-based models integrating clinicopathological features and molecular markers as variables are helpful in selecting the patients of OSCC with high risk of postoperative distant metastasis. Nature Publishing Group 2013-09-03 2013-08-13 /pmc/articles/PMC3778272/ /pubmed/23942069 http://dx.doi.org/10.1038/bjc.2013.379 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Yang, H X
Feng, W
Wei, J C
Zeng, T S
Li, Z D
Zhang, L J
Lin, P
Luo, R Z
He, J H
Fu, J H
Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
title Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
title_full Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
title_fullStr Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
title_full_unstemmed Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
title_short Support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
title_sort support vector machine-based nomogram predicts postoperative distant metastasis for patients with oesophageal squamous cell carcinoma
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778272/
https://www.ncbi.nlm.nih.gov/pubmed/23942069
http://dx.doi.org/10.1038/bjc.2013.379
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