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Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors

PURPOSE: The objective of this study was to establish a predictive nomogram based on ultrasound (US) and clinical features for patients with soft tissue tumors (STTs). PATIENTS AND METHODS: A total of 260 patients with STTs were enrolled in this retrospective study and were divided into a training c...

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Autores principales: Wu, Mengjie, Hu, Yu, Ren, Anjing, Peng, Xiaojing, Ma, Qian, Mao, Cuilian, Hang, Jing, Li, Ao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936676/
https://www.ncbi.nlm.nih.gov/pubmed/33688257
http://dx.doi.org/10.2147/CMAR.S296972
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author Wu, Mengjie
Hu, Yu
Ren, Anjing
Peng, Xiaojing
Ma, Qian
Mao, Cuilian
Hang, Jing
Li, Ao
author_facet Wu, Mengjie
Hu, Yu
Ren, Anjing
Peng, Xiaojing
Ma, Qian
Mao, Cuilian
Hang, Jing
Li, Ao
author_sort Wu, Mengjie
collection PubMed
description PURPOSE: The objective of this study was to establish a predictive nomogram based on ultrasound (US) and clinical features for patients with soft tissue tumors (STTs). PATIENTS AND METHODS: A total of 260 patients with STTs were enrolled in this retrospective study and were divided into a training cohort (n=200, including 110 malignant and 90 benign masses) and a validation cohort (n=60, including 30 malignant and 30 benign masses). Multivariate analysis was performed by binary logistic regression analysis to determine the significant factors predictive of malignancy. A simple nomogram was established based on these independent risk factors including US and clinical features. The predictive accuracy and discriminative ability of the nomogram were measured by the calibration curve and the concordance index (C-index). RESULTS: The nomogram, comprising US features (maximum diameter, margin and vascular density) and clinical features (sex, age, and duration of disease), showed a favorable performance for predicting malignancy, with a sensitivity of 88.2% and a specificity of 78.7%. The calibration curve for malignancy probability in the training cohort showed good agreement between the nomogram predictions and actual observations. The C-indexes of the training cohort and validation cohort for predicting malignancy were 0.89 (95% CI: 0.85–0.94) and 0.83 (95% CI: 0.73–0.94), respectively. CONCLUSION: The nomogram based on US and clinical features could be a simple, intuitive and reliable tool to individually predict malignancy in patients with STTs.
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spelling pubmed-79366762021-03-08 Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors Wu, Mengjie Hu, Yu Ren, Anjing Peng, Xiaojing Ma, Qian Mao, Cuilian Hang, Jing Li, Ao Cancer Manag Res Original Research PURPOSE: The objective of this study was to establish a predictive nomogram based on ultrasound (US) and clinical features for patients with soft tissue tumors (STTs). PATIENTS AND METHODS: A total of 260 patients with STTs were enrolled in this retrospective study and were divided into a training cohort (n=200, including 110 malignant and 90 benign masses) and a validation cohort (n=60, including 30 malignant and 30 benign masses). Multivariate analysis was performed by binary logistic regression analysis to determine the significant factors predictive of malignancy. A simple nomogram was established based on these independent risk factors including US and clinical features. The predictive accuracy and discriminative ability of the nomogram were measured by the calibration curve and the concordance index (C-index). RESULTS: The nomogram, comprising US features (maximum diameter, margin and vascular density) and clinical features (sex, age, and duration of disease), showed a favorable performance for predicting malignancy, with a sensitivity of 88.2% and a specificity of 78.7%. The calibration curve for malignancy probability in the training cohort showed good agreement between the nomogram predictions and actual observations. The C-indexes of the training cohort and validation cohort for predicting malignancy were 0.89 (95% CI: 0.85–0.94) and 0.83 (95% CI: 0.73–0.94), respectively. CONCLUSION: The nomogram based on US and clinical features could be a simple, intuitive and reliable tool to individually predict malignancy in patients with STTs. Dove 2021-03-02 /pmc/articles/PMC7936676/ /pubmed/33688257 http://dx.doi.org/10.2147/CMAR.S296972 Text en © 2021 Wu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wu, Mengjie
Hu, Yu
Ren, Anjing
Peng, Xiaojing
Ma, Qian
Mao, Cuilian
Hang, Jing
Li, Ao
Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors
title Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors
title_full Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors
title_fullStr Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors
title_full_unstemmed Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors
title_short Nomogram Based on Ultrasonography and Clinical Features for Predicting Malignancy in Soft Tissue Tumors
title_sort nomogram based on ultrasonography and clinical features for predicting malignancy in soft tissue tumors
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936676/
https://www.ncbi.nlm.nih.gov/pubmed/33688257
http://dx.doi.org/10.2147/CMAR.S296972
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