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The Differential Diagnostic Value of Radiomics Signatures Between Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients with Colorectal Cancer
BACKGROUND: Differential diagnosis of single-nodule pulmonary metastasis (SNPM) and second primary lung cancer (SPLC) in patients with colorectal cancer (CRC) prior to lung surgery is relatively complex. Radiomics is an emerging technique for image information analysis, while it has not yet been app...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226291/ https://www.ncbi.nlm.nih.gov/pubmed/37226476 http://dx.doi.org/10.1177/15330338231175735 |
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author | Yu, Yu Tan, Jiaqing Yang, Yi Zhang, Bin Yao, Xiaodong Sang, Shibiao Deng, Shengming |
author_facet | Yu, Yu Tan, Jiaqing Yang, Yi Zhang, Bin Yao, Xiaodong Sang, Shibiao Deng, Shengming |
author_sort | Yu, Yu |
collection | PubMed |
description | BACKGROUND: Differential diagnosis of single-nodule pulmonary metastasis (SNPM) and second primary lung cancer (SPLC) in patients with colorectal cancer (CRC) prior to lung surgery is relatively complex. Radiomics is an emerging technique for image information analysis, while it has not yet been applied to construct a differential diagnostic model between SNPM and SPLC in patients with CRC. In the present study, we aimed to extract radiomics signatures from thin-section computed tomography (CT) images of the chest. These radiomics signatures were combined with clinical features to construct a composite differential diagnostic model. METHOD: A total of 91 patients with CRC, including 66 patients with SNPM and 25 patients with SPLC, were enrolled in this study. Patients were randomly assigned to the training cohort (n = 63) and validation cohort (n = 28) at a ratio of 7 to 3. Moreover, 107 radiomics features were extracted from the chest thin-section CT images. The least absolute shrinkage and selection operator (LASSO) regression was used to filter these features, and clinical features were screened by univariate analysis. The screened radiomics and clinical features were combined to construct a multifactorial logistic regression composite model. The receiver operating characteristic (ROC) curves were adopted to evaluate the models, and the corresponding nomograms were created. RESULTS: A series of 6 radiomics characteristics was screened by LASSO. After univariate logistic regression analysis, the composite model finally included 4 radiomics features and 4 clinical features. In the training cohort, the area under the curve scores of ROC curves were 0.912 (95% confidence interval [CI]: 0.813-0.969), 0.884 (95% CI: 0.778-0.951), and 0.939 (95% CI: 0.848-0.984) for models derived from radiomics, clinical, and combined features, respectively. Similarly, these values were 0.756 (95% CI: 0.558-0.897), 0.888 (95% CI: 0.711-0.975), and 0.950 (95% CI: 0.795-0.997) in the validation cohort, respectively. CONCLUSIONS: We constructed a model for differential diagnosis of SNPM and SPLC in patients with CRC using radiomics and clinical features. Moreover, our findings provided a new assessment tool for patients with CRC in the future. |
format | Online Article Text |
id | pubmed-10226291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-102262912023-05-30 The Differential Diagnostic Value of Radiomics Signatures Between Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients with Colorectal Cancer Yu, Yu Tan, Jiaqing Yang, Yi Zhang, Bin Yao, Xiaodong Sang, Shibiao Deng, Shengming Technol Cancer Res Treat Original Article BACKGROUND: Differential diagnosis of single-nodule pulmonary metastasis (SNPM) and second primary lung cancer (SPLC) in patients with colorectal cancer (CRC) prior to lung surgery is relatively complex. Radiomics is an emerging technique for image information analysis, while it has not yet been applied to construct a differential diagnostic model between SNPM and SPLC in patients with CRC. In the present study, we aimed to extract radiomics signatures from thin-section computed tomography (CT) images of the chest. These radiomics signatures were combined with clinical features to construct a composite differential diagnostic model. METHOD: A total of 91 patients with CRC, including 66 patients with SNPM and 25 patients with SPLC, were enrolled in this study. Patients were randomly assigned to the training cohort (n = 63) and validation cohort (n = 28) at a ratio of 7 to 3. Moreover, 107 radiomics features were extracted from the chest thin-section CT images. The least absolute shrinkage and selection operator (LASSO) regression was used to filter these features, and clinical features were screened by univariate analysis. The screened radiomics and clinical features were combined to construct a multifactorial logistic regression composite model. The receiver operating characteristic (ROC) curves were adopted to evaluate the models, and the corresponding nomograms were created. RESULTS: A series of 6 radiomics characteristics was screened by LASSO. After univariate logistic regression analysis, the composite model finally included 4 radiomics features and 4 clinical features. In the training cohort, the area under the curve scores of ROC curves were 0.912 (95% confidence interval [CI]: 0.813-0.969), 0.884 (95% CI: 0.778-0.951), and 0.939 (95% CI: 0.848-0.984) for models derived from radiomics, clinical, and combined features, respectively. Similarly, these values were 0.756 (95% CI: 0.558-0.897), 0.888 (95% CI: 0.711-0.975), and 0.950 (95% CI: 0.795-0.997) in the validation cohort, respectively. CONCLUSIONS: We constructed a model for differential diagnosis of SNPM and SPLC in patients with CRC using radiomics and clinical features. Moreover, our findings provided a new assessment tool for patients with CRC in the future. SAGE Publications 2023-05-24 /pmc/articles/PMC10226291/ /pubmed/37226476 http://dx.doi.org/10.1177/15330338231175735 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Yu, Yu Tan, Jiaqing Yang, Yi Zhang, Bin Yao, Xiaodong Sang, Shibiao Deng, Shengming The Differential Diagnostic Value of Radiomics Signatures Between Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients with Colorectal Cancer |
title | The Differential Diagnostic Value of Radiomics Signatures Between
Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients
with Colorectal Cancer |
title_full | The Differential Diagnostic Value of Radiomics Signatures Between
Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients
with Colorectal Cancer |
title_fullStr | The Differential Diagnostic Value of Radiomics Signatures Between
Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients
with Colorectal Cancer |
title_full_unstemmed | The Differential Diagnostic Value of Radiomics Signatures Between
Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients
with Colorectal Cancer |
title_short | The Differential Diagnostic Value of Radiomics Signatures Between
Single-Nodule Pulmonary Metastases and Second Primary Lung Cancer in Patients
with Colorectal Cancer |
title_sort | differential diagnostic value of radiomics signatures between
single-nodule pulmonary metastases and second primary lung cancer in patients
with colorectal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226291/ https://www.ncbi.nlm.nih.gov/pubmed/37226476 http://dx.doi.org/10.1177/15330338231175735 |
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