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Predicting survival time of lung cancer patients using radiomic analysis

OBJECTIVES: This study investigates the prediction of Non-small cell lung cancer (NSCLC) patient survival outcomes based on radiomic texture and shape features automatically extracted from tumor image data. MATERIALS AND METHODS: Retrospective analysis involves CT scans of 315 NSCLC patients from Th...

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Autores principales: Chaddad, Ahmad, Desrosiers, Christian, Toews, Matthew, Abdulkarim, Bassam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732814/
https://www.ncbi.nlm.nih.gov/pubmed/29262648
http://dx.doi.org/10.18632/oncotarget.22251
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author Chaddad, Ahmad
Desrosiers, Christian
Toews, Matthew
Abdulkarim, Bassam
author_facet Chaddad, Ahmad
Desrosiers, Christian
Toews, Matthew
Abdulkarim, Bassam
author_sort Chaddad, Ahmad
collection PubMed
description OBJECTIVES: This study investigates the prediction of Non-small cell lung cancer (NSCLC) patient survival outcomes based on radiomic texture and shape features automatically extracted from tumor image data. MATERIALS AND METHODS: Retrospective analysis involves CT scans of 315 NSCLC patients from The Cancer Imaging Archive (TCIA). A total of 24 image features are computed from labeled tumor volumes of patients within groups defined using NSCLC subtype and TNM staging information. Spearman’s rank correlation, Kaplan-Meier estimation and log-rank tests were used to identify features related to long/short NSCLC patient survival groups. Automatic random forest classification was used to predict patient survival group from multivariate feature data. Significance is assessed at P < 0.05 following Holm-Bonferroni correction for multiple comparisons. RESULTS: Significant correlations between radiomic features and survival were observed for four clinical groups: (group, [absolute correlation range]): (large cell carcinoma (LCC) [0.35, 0.43]), (tumor size T2, [0.31, 0.39]), (non lymph node metastasis N0, [0.3, 0.33]), (TNM stage I, [0.39, 0.48]). Significant log-rank relationships between features and survival time were observed for three clinical groups: (group, hazard ratio): (LCC, 3.0), (LCC, 3.9), (T2, 2.5) and (stage I, 2.9). Automatic survival prediction performance (i.e. below/above median) is superior for combined radiomic features with age-TNM in comparison to standard TNM clinical staging information (clinical group, mean area-under-the-ROC-curve (AUC)): (LCC, 75.73%), (N0, 70.33%), (T2, 70.28%) and (TNM-I, 76.17%). CONCLUSION: Quantitative lung CT imaging features can be used as indicators of survival, in particular for patients with large-cell-carcinoma (LCC), primary-tumor-sizes (T2) and no lymph-node-metastasis (N0).
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spelling pubmed-57328142017-12-19 Predicting survival time of lung cancer patients using radiomic analysis Chaddad, Ahmad Desrosiers, Christian Toews, Matthew Abdulkarim, Bassam Oncotarget Research Paper OBJECTIVES: This study investigates the prediction of Non-small cell lung cancer (NSCLC) patient survival outcomes based on radiomic texture and shape features automatically extracted from tumor image data. MATERIALS AND METHODS: Retrospective analysis involves CT scans of 315 NSCLC patients from The Cancer Imaging Archive (TCIA). A total of 24 image features are computed from labeled tumor volumes of patients within groups defined using NSCLC subtype and TNM staging information. Spearman’s rank correlation, Kaplan-Meier estimation and log-rank tests were used to identify features related to long/short NSCLC patient survival groups. Automatic random forest classification was used to predict patient survival group from multivariate feature data. Significance is assessed at P < 0.05 following Holm-Bonferroni correction for multiple comparisons. RESULTS: Significant correlations between radiomic features and survival were observed for four clinical groups: (group, [absolute correlation range]): (large cell carcinoma (LCC) [0.35, 0.43]), (tumor size T2, [0.31, 0.39]), (non lymph node metastasis N0, [0.3, 0.33]), (TNM stage I, [0.39, 0.48]). Significant log-rank relationships between features and survival time were observed for three clinical groups: (group, hazard ratio): (LCC, 3.0), (LCC, 3.9), (T2, 2.5) and (stage I, 2.9). Automatic survival prediction performance (i.e. below/above median) is superior for combined radiomic features with age-TNM in comparison to standard TNM clinical staging information (clinical group, mean area-under-the-ROC-curve (AUC)): (LCC, 75.73%), (N0, 70.33%), (T2, 70.28%) and (TNM-I, 76.17%). CONCLUSION: Quantitative lung CT imaging features can be used as indicators of survival, in particular for patients with large-cell-carcinoma (LCC), primary-tumor-sizes (T2) and no lymph-node-metastasis (N0). Impact Journals LLC 2017-11-01 /pmc/articles/PMC5732814/ /pubmed/29262648 http://dx.doi.org/10.18632/oncotarget.22251 Text en Copyright: © 2017 Chaddad 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
Chaddad, Ahmad
Desrosiers, Christian
Toews, Matthew
Abdulkarim, Bassam
Predicting survival time of lung cancer patients using radiomic analysis
title Predicting survival time of lung cancer patients using radiomic analysis
title_full Predicting survival time of lung cancer patients using radiomic analysis
title_fullStr Predicting survival time of lung cancer patients using radiomic analysis
title_full_unstemmed Predicting survival time of lung cancer patients using radiomic analysis
title_short Predicting survival time of lung cancer patients using radiomic analysis
title_sort predicting survival time of lung cancer patients using radiomic analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732814/
https://www.ncbi.nlm.nih.gov/pubmed/29262648
http://dx.doi.org/10.18632/oncotarget.22251
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