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Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma
BACKGROUND: The aim of the study was to investigate the value of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and intravoxel incoherent motion (IVIM) in differentiating TP53-mutant from wild type, low-risk from non-low-risk early-stage endometrial carcinoma (EC). PATIENTS AND METHO...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sciendo
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286889/ https://www.ncbi.nlm.nih.gov/pubmed/37341203 http://dx.doi.org/10.2478/raon-2023-0023 |
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author | Wang, Hongxia Yan, Ruifang Li, Zhong Wang, Beiran Jin, Xingxing Guo, Zhenfang Liu, Wangyi Zhang, Meng Wang, Kaiyu Guo, Jinxia Han, Dongming |
author_facet | Wang, Hongxia Yan, Ruifang Li, Zhong Wang, Beiran Jin, Xingxing Guo, Zhenfang Liu, Wangyi Zhang, Meng Wang, Kaiyu Guo, Jinxia Han, Dongming |
author_sort | Wang, Hongxia |
collection | PubMed |
description | BACKGROUND: The aim of the study was to investigate the value of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and intravoxel incoherent motion (IVIM) in differentiating TP53-mutant from wild type, low-risk from non-low-risk early-stage endometrial carcinoma (EC). PATIENTS AND METHODS: A total of 74 EC patients underwent pelvic MRI. Parameters volume transfer constant (K(trans)), rate transfer constant (K(ep)), the volume of extravascular extracellular space per unit volume of tissue (V(e)), true diffusion coefficient (D), pseudo-diffusion coefficient (D*), and microvascular volume fraction (f) were compared. The combination of parameters was investigated by logistic regression and evaluated by bootstrap (1000 samples), receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA). RESULTS: In the TP53-mutant group, K(trans) and K(ep) were higher and D was lower than in the TP53-wild group; K(trans), V(e), f, and D were lower in the non-low-risk group than in the low-risk group (all P < 0.05). In the identification of TP53-mutant and TP53-wild early-stage EC, K(trans) and D were independent predictors, and the combination of them had an optimal diagnostic efficacy (AUC, 0.867; sensitivity, 92.00%; specificity, 80.95%), which was significantly better than D (Z = 2.169, P = 0.030) and K(trans) (Z = 2.572, P = 0.010). In the identification of low-risk and non-low-risk early-stage EC, K(trans), V(e), and f were independent predictors, and the combination of them had an optimal diagnostic efficacy (AUC, 0.947; sensitivity, 83.33%; specificity, 93.18%), which was significantly better than D (Z = 3.113, P = 0.002), f (Z = 4.317, P < 0.001), K(trans) (Z = 2.713, P = 0.007), and V(e) (Z = 3.175, P = 0.002). The calibration curves showed that the above two combinations of independent predictors, both have good consistency, and DCA showed that these combinations were reliable clinical prediction tools. CONCLUSIONS: Both DCE-MRI and IVIM facilitate the prediction of TP53 status and risk stratification in early-stage EC. Compare with each single parameter, the combination of independent predictors provided better predictive power and may serve as a superior imaging marker. |
format | Online Article Text |
id | pubmed-10286889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Sciendo |
record_format | MEDLINE/PubMed |
spelling | pubmed-102868892023-06-23 Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma Wang, Hongxia Yan, Ruifang Li, Zhong Wang, Beiran Jin, Xingxing Guo, Zhenfang Liu, Wangyi Zhang, Meng Wang, Kaiyu Guo, Jinxia Han, Dongming Radiol Oncol Research Article BACKGROUND: The aim of the study was to investigate the value of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and intravoxel incoherent motion (IVIM) in differentiating TP53-mutant from wild type, low-risk from non-low-risk early-stage endometrial carcinoma (EC). PATIENTS AND METHODS: A total of 74 EC patients underwent pelvic MRI. Parameters volume transfer constant (K(trans)), rate transfer constant (K(ep)), the volume of extravascular extracellular space per unit volume of tissue (V(e)), true diffusion coefficient (D), pseudo-diffusion coefficient (D*), and microvascular volume fraction (f) were compared. The combination of parameters was investigated by logistic regression and evaluated by bootstrap (1000 samples), receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA). RESULTS: In the TP53-mutant group, K(trans) and K(ep) were higher and D was lower than in the TP53-wild group; K(trans), V(e), f, and D were lower in the non-low-risk group than in the low-risk group (all P < 0.05). In the identification of TP53-mutant and TP53-wild early-stage EC, K(trans) and D were independent predictors, and the combination of them had an optimal diagnostic efficacy (AUC, 0.867; sensitivity, 92.00%; specificity, 80.95%), which was significantly better than D (Z = 2.169, P = 0.030) and K(trans) (Z = 2.572, P = 0.010). In the identification of low-risk and non-low-risk early-stage EC, K(trans), V(e), and f were independent predictors, and the combination of them had an optimal diagnostic efficacy (AUC, 0.947; sensitivity, 83.33%; specificity, 93.18%), which was significantly better than D (Z = 3.113, P = 0.002), f (Z = 4.317, P < 0.001), K(trans) (Z = 2.713, P = 0.007), and V(e) (Z = 3.175, P = 0.002). The calibration curves showed that the above two combinations of independent predictors, both have good consistency, and DCA showed that these combinations were reliable clinical prediction tools. CONCLUSIONS: Both DCE-MRI and IVIM facilitate the prediction of TP53 status and risk stratification in early-stage EC. Compare with each single parameter, the combination of independent predictors provided better predictive power and may serve as a superior imaging marker. Sciendo 2023-06-21 /pmc/articles/PMC10286889/ /pubmed/37341203 http://dx.doi.org/10.2478/raon-2023-0023 Text en © 2023 Hongxia Wang et al., published by Sciendo https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. |
spellingShingle | Research Article Wang, Hongxia Yan, Ruifang Li, Zhong Wang, Beiran Jin, Xingxing Guo, Zhenfang Liu, Wangyi Zhang, Meng Wang, Kaiyu Guo, Jinxia Han, Dongming Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma |
title | Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma |
title_full | Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma |
title_fullStr | Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma |
title_full_unstemmed | Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma |
title_short | Quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of TP53 status and risk stratification of early-stage endometrial carcinoma |
title_sort | quantitative dynamic contrast-enhanced parameters and intravoxel incoherent motion facilitate the prediction of tp53 status and risk stratification of early-stage endometrial carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286889/ https://www.ncbi.nlm.nih.gov/pubmed/37341203 http://dx.doi.org/10.2478/raon-2023-0023 |
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