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Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces
BACKGROUND: Tumor spread through air spaces (STAS) is an important pattern of invasion and impacts the frequency and location of recurrence. The objective was to assess the correlation between metabolic tumor burden of positron emission tomography/computed tomography (PET/CT) and 2015 World Health O...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798457/ https://www.ncbi.nlm.nih.gov/pubmed/35117249 http://dx.doi.org/10.21037/tcr-20-1934 |
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author | Wang, Xiao-Yi Zhao, Yan-Feng Yang, Lin Liu, Ying Yang, Yi-Kun Wu, Ning |
author_facet | Wang, Xiao-Yi Zhao, Yan-Feng Yang, Lin Liu, Ying Yang, Yi-Kun Wu, Ning |
author_sort | Wang, Xiao-Yi |
collection | PubMed |
description | BACKGROUND: Tumor spread through air spaces (STAS) is an important pattern of invasion and impacts the frequency and location of recurrence. The objective was to assess the correlation between metabolic tumor burden of positron emission tomography/computed tomography (PET/CT) and 2015 World Health Organization (WHO) classification of lung adenocarcinoma, and to establish a risk prediction model of STAS. METHODS: We reviewed 127 consecutive patients. The SUV(max), SUV(mean), SUV(peak), MTV, TLG, diameter, and CTV were measured. All risk factors were analyzed by multivariate logistic regression analysis; regression coefficients and odds ratios were calculated for independent risk factors. A STAS risk prediction model was created using the regression coefficients to determine the predictive probability (PP). RESULTS: The nodule types and SUV were significantly correlated with 2015 WHO pathological categories (P<0.001). Most of (83.3%) the lepidic predominant adenocarcinoma (LPA) appeared as non-solid or part-solid nodules with the lowest SUV (P<0.05). There was a significant difference in STAS distribution among different nodule types (P=0.000). STAS was significantly correlated with SUV(max) (P=0.000), SUV(mean) (P=0.000), SUV(peak) (P=0.000), TLG (P=0.001), and diameter (P=0.044). The risk prediction model of STAS was established. The PP of STAS and the incidence of STAS were analyzed using the ROC curve (AUC =0.759, P=0.000). The sensitivity, specificity, and accuracy of the predictive model for STAS were 47.1%, 88.6%, and 71.1%, respectively. CONCLUSIONS: The LPA appeared as non-solid nodule with low SUV without STAS has a good prognosis. SUV and TLG are valuable predictive indices in the prediction of STAS. The predictive model developed in predicting the incidence of STAS has good specificity and accuracy. |
format | Online Article Text |
id | pubmed-8798457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87984572022-02-02 Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces Wang, Xiao-Yi Zhao, Yan-Feng Yang, Lin Liu, Ying Yang, Yi-Kun Wu, Ning Transl Cancer Res Original Article BACKGROUND: Tumor spread through air spaces (STAS) is an important pattern of invasion and impacts the frequency and location of recurrence. The objective was to assess the correlation between metabolic tumor burden of positron emission tomography/computed tomography (PET/CT) and 2015 World Health Organization (WHO) classification of lung adenocarcinoma, and to establish a risk prediction model of STAS. METHODS: We reviewed 127 consecutive patients. The SUV(max), SUV(mean), SUV(peak), MTV, TLG, diameter, and CTV were measured. All risk factors were analyzed by multivariate logistic regression analysis; regression coefficients and odds ratios were calculated for independent risk factors. A STAS risk prediction model was created using the regression coefficients to determine the predictive probability (PP). RESULTS: The nodule types and SUV were significantly correlated with 2015 WHO pathological categories (P<0.001). Most of (83.3%) the lepidic predominant adenocarcinoma (LPA) appeared as non-solid or part-solid nodules with the lowest SUV (P<0.05). There was a significant difference in STAS distribution among different nodule types (P=0.000). STAS was significantly correlated with SUV(max) (P=0.000), SUV(mean) (P=0.000), SUV(peak) (P=0.000), TLG (P=0.001), and diameter (P=0.044). The risk prediction model of STAS was established. The PP of STAS and the incidence of STAS were analyzed using the ROC curve (AUC =0.759, P=0.000). The sensitivity, specificity, and accuracy of the predictive model for STAS were 47.1%, 88.6%, and 71.1%, respectively. CONCLUSIONS: The LPA appeared as non-solid nodule with low SUV without STAS has a good prognosis. SUV and TLG are valuable predictive indices in the prediction of STAS. The predictive model developed in predicting the incidence of STAS has good specificity and accuracy. AME Publishing Company 2020-10 /pmc/articles/PMC8798457/ /pubmed/35117249 http://dx.doi.org/10.21037/tcr-20-1934 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Wang, Xiao-Yi Zhao, Yan-Feng Yang, Lin Liu, Ying Yang, Yi-Kun Wu, Ning Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
title | Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
title_full | Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
title_fullStr | Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
title_full_unstemmed | Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
title_short | Correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 World Health Organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
title_sort | correlation analysis between metabolic tumor burden measured by positron emission tomography/computed tomography and the 2015 world health organization classification of lung adenocarcinoma, with a risk prediction model of tumor spread through air spaces |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798457/ https://www.ncbi.nlm.nih.gov/pubmed/35117249 http://dx.doi.org/10.21037/tcr-20-1934 |
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