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Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma

There is no consensus on specific prognostic biomarkers potentially improving survival of nasopharyngeal carcinoma (NPC), especially in advanced-stage disease. The prognostic value of MRI-based radiomics signature is unclear. A total of 970 quantitative features were extracted from the tumor of 100...

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Autores principales: Ouyang, Fu-Sheng, Guo, Bao-Liang, Zhang, Bin, Dong, Yu-Hao, Zhang, Lu, Mo, Xiao-Kai, Huang, Wen-Hui, Zhang, Shui-Xing, Hu, Qiu-Gen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650385/
https://www.ncbi.nlm.nih.gov/pubmed/29088830
http://dx.doi.org/10.18632/oncotarget.20423
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author Ouyang, Fu-Sheng
Guo, Bao-Liang
Zhang, Bin
Dong, Yu-Hao
Zhang, Lu
Mo, Xiao-Kai
Huang, Wen-Hui
Zhang, Shui-Xing
Hu, Qiu-Gen
author_facet Ouyang, Fu-Sheng
Guo, Bao-Liang
Zhang, Bin
Dong, Yu-Hao
Zhang, Lu
Mo, Xiao-Kai
Huang, Wen-Hui
Zhang, Shui-Xing
Hu, Qiu-Gen
author_sort Ouyang, Fu-Sheng
collection PubMed
description There is no consensus on specific prognostic biomarkers potentially improving survival of nasopharyngeal carcinoma (NPC), especially in advanced-stage disease. The prognostic value of MRI-based radiomics signature is unclear. A total of 970 quantitative features were extracted from the tumor of 100 untreated NPC patients (stage III-IVb) (discovery set: n = 70, validation set: n = 30). We then applied least absolute shrinkage and selection operator (lasso) regression to select features that were most associated with progression-free survival (PFS). Candidate prognostic biomarkers included age, gender, overall stage, hemoglobin, platelet counts and radiomics signature. We developed model 1 (without radiomics signature) and model 2 (with radiomics signature) in the discovery set and then tested in the validation set. Multivariable Cox regression analysis was used to yield hazard ratio (HR) of each potential biomarker. We found the radiomics signature stratified patients in the discovery set into a low or high risk group for PFS (HR = 5.14, p < 0.001) and was successfully validated for patients in the validation set (HR = 7.28, p = 0.015). However, the other risk factors showed no significantly prognostic value (all p-values for HR, > 0.05). Accordingly, pretreatment MRI-based radiomics signature is a non-invasive and cost-effective prognostic biomarker in advanced NPC patients, which would improve decision-support in cancer care.
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spelling pubmed-56503852017-10-30 Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma Ouyang, Fu-Sheng Guo, Bao-Liang Zhang, Bin Dong, Yu-Hao Zhang, Lu Mo, Xiao-Kai Huang, Wen-Hui Zhang, Shui-Xing Hu, Qiu-Gen Oncotarget Research Paper There is no consensus on specific prognostic biomarkers potentially improving survival of nasopharyngeal carcinoma (NPC), especially in advanced-stage disease. The prognostic value of MRI-based radiomics signature is unclear. A total of 970 quantitative features were extracted from the tumor of 100 untreated NPC patients (stage III-IVb) (discovery set: n = 70, validation set: n = 30). We then applied least absolute shrinkage and selection operator (lasso) regression to select features that were most associated with progression-free survival (PFS). Candidate prognostic biomarkers included age, gender, overall stage, hemoglobin, platelet counts and radiomics signature. We developed model 1 (without radiomics signature) and model 2 (with radiomics signature) in the discovery set and then tested in the validation set. Multivariable Cox regression analysis was used to yield hazard ratio (HR) of each potential biomarker. We found the radiomics signature stratified patients in the discovery set into a low or high risk group for PFS (HR = 5.14, p < 0.001) and was successfully validated for patients in the validation set (HR = 7.28, p = 0.015). However, the other risk factors showed no significantly prognostic value (all p-values for HR, > 0.05). Accordingly, pretreatment MRI-based radiomics signature is a non-invasive and cost-effective prognostic biomarker in advanced NPC patients, which would improve decision-support in cancer care. Impact Journals LLC 2017-08-24 /pmc/articles/PMC5650385/ /pubmed/29088830 http://dx.doi.org/10.18632/oncotarget.20423 Text en Copyright: © 2017 Ouyang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ouyang, Fu-Sheng
Guo, Bao-Liang
Zhang, Bin
Dong, Yu-Hao
Zhang, Lu
Mo, Xiao-Kai
Huang, Wen-Hui
Zhang, Shui-Xing
Hu, Qiu-Gen
Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma
title Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma
title_full Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma
title_fullStr Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma
title_full_unstemmed Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma
title_short Exploration and validation of radiomics signature as an independent prognostic biomarker in stage III-IVb nasopharyngeal carcinoma
title_sort exploration and validation of radiomics signature as an independent prognostic biomarker in stage iii-ivb nasopharyngeal carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650385/
https://www.ncbi.nlm.nih.gov/pubmed/29088830
http://dx.doi.org/10.18632/oncotarget.20423
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