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Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis
This was a retrospective study to investigate the predictive and prognostic ability of quantitative computed tomography phenotypic features in patients with non-small cell lung cancer (NSCLC). 661 patients with pathological confirmed as NSCLC were enrolled between 2007 and 2014. 592 phenotypic descr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138817/ https://www.ncbi.nlm.nih.gov/pubmed/27922113 http://dx.doi.org/10.1038/srep38282 |
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author | Song, Jiangdian Liu, Zaiyi Zhong, Wenzhao Huang, Yanqi Ma, Zelan Dong, Di Liang, Changhong Tian, Jie |
author_facet | Song, Jiangdian Liu, Zaiyi Zhong, Wenzhao Huang, Yanqi Ma, Zelan Dong, Di Liang, Changhong Tian, Jie |
author_sort | Song, Jiangdian |
collection | PubMed |
description | This was a retrospective study to investigate the predictive and prognostic ability of quantitative computed tomography phenotypic features in patients with non-small cell lung cancer (NSCLC). 661 patients with pathological confirmed as NSCLC were enrolled between 2007 and 2014. 592 phenotypic descriptors was automatically extracted on the pre-therapy CT images. Firstly, support vector machine (SVM) was used to evaluate the predictive value of each feature for pathology and TNM clinical stage. Secondly, Cox proportional hazards model was used to evaluate the prognostic value of these imaging signatures selected by SVM which subjected to a primary cohort of 138 patients, and an external independent validation of 61 patients. The results indicated that predictive accuracy for histopathology, N staging, and overall clinical stage was 75.16%, 79.40% and 80.33%, respectively. Besides, Cox models indicated the signatures selected by SVM: “correlation of co-occurrence after wavelet transform” was significantly associated with overall survival in the two datasets (hazard ratio [HR]: 1.65, 95% confidence interval [CI]: 1.41–2.75, p = 0.010; and HR: 2.74, 95%CI: 1.10–6.85, p = 0.027, respectively). Our study indicates that the phenotypic features might provide some insight in metastatic potential or aggressiveness for NSCLC, which potentially offer clinical value in directing personalized therapeutic regimen selection for NSCLC. |
format | Online Article Text |
id | pubmed-5138817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51388172016-12-16 Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis Song, Jiangdian Liu, Zaiyi Zhong, Wenzhao Huang, Yanqi Ma, Zelan Dong, Di Liang, Changhong Tian, Jie Sci Rep Article This was a retrospective study to investigate the predictive and prognostic ability of quantitative computed tomography phenotypic features in patients with non-small cell lung cancer (NSCLC). 661 patients with pathological confirmed as NSCLC were enrolled between 2007 and 2014. 592 phenotypic descriptors was automatically extracted on the pre-therapy CT images. Firstly, support vector machine (SVM) was used to evaluate the predictive value of each feature for pathology and TNM clinical stage. Secondly, Cox proportional hazards model was used to evaluate the prognostic value of these imaging signatures selected by SVM which subjected to a primary cohort of 138 patients, and an external independent validation of 61 patients. The results indicated that predictive accuracy for histopathology, N staging, and overall clinical stage was 75.16%, 79.40% and 80.33%, respectively. Besides, Cox models indicated the signatures selected by SVM: “correlation of co-occurrence after wavelet transform” was significantly associated with overall survival in the two datasets (hazard ratio [HR]: 1.65, 95% confidence interval [CI]: 1.41–2.75, p = 0.010; and HR: 2.74, 95%CI: 1.10–6.85, p = 0.027, respectively). Our study indicates that the phenotypic features might provide some insight in metastatic potential or aggressiveness for NSCLC, which potentially offer clinical value in directing personalized therapeutic regimen selection for NSCLC. Nature Publishing Group 2016-12-06 /pmc/articles/PMC5138817/ /pubmed/27922113 http://dx.doi.org/10.1038/srep38282 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Song, Jiangdian Liu, Zaiyi Zhong, Wenzhao Huang, Yanqi Ma, Zelan Dong, Di Liang, Changhong Tian, Jie Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis |
title | Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis |
title_full | Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis |
title_fullStr | Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis |
title_full_unstemmed | Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis |
title_short | Non-small cell lung cancer: quantitative phenotypic analysis of CT images as a potential marker of prognosis |
title_sort | non-small cell lung cancer: quantitative phenotypic analysis of ct images as a potential marker of prognosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138817/ https://www.ncbi.nlm.nih.gov/pubmed/27922113 http://dx.doi.org/10.1038/srep38282 |
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