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Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors

PURPOSE: To build radiomic prediction models using contrast-enhanced computed tomography (CE-CT) to preoperatively predict malignant potential and mitotic count of gastrointestinal stromal tumors (GISTs). PATIENTS AND METHODS: A total of 333 GISTs patients were retrospectively included in our study....

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Autores principales: Wang, Chao, Li, Hailin, Jiaerken, Yeerfan, Huang, Peiyu, Sun, Lifeng, Dong, Fei, Huang, Yajing, Dong, Di, Tian, Jie, Zhang, Minming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614115/
https://www.ncbi.nlm.nih.gov/pubmed/31280094
http://dx.doi.org/10.1016/j.tranon.2019.06.005
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author Wang, Chao
Li, Hailin
Jiaerken, Yeerfan
Huang, Peiyu
Sun, Lifeng
Dong, Fei
Huang, Yajing
Dong, Di
Tian, Jie
Zhang, Minming
author_facet Wang, Chao
Li, Hailin
Jiaerken, Yeerfan
Huang, Peiyu
Sun, Lifeng
Dong, Fei
Huang, Yajing
Dong, Di
Tian, Jie
Zhang, Minming
author_sort Wang, Chao
collection PubMed
description PURPOSE: To build radiomic prediction models using contrast-enhanced computed tomography (CE-CT) to preoperatively predict malignant potential and mitotic count of gastrointestinal stromal tumors (GISTs). PATIENTS AND METHODS: A total of 333 GISTs patients were retrospectively included in our study. Radiomic features were extracted from the preoperative CE-CT images. According to postoperative pathology, patients were categorized by malignant potential and mitotic count, respectively. The most valuable radiomic features were chosen to build a logistic regression model to predict the malignant potential and a random forest classifier model to predict the mitotic count. The performance of radiomic models was assessed with the receiver operating characteristics curve. Our study further developed a radiomic nomogram to preoperatively predict malignant potential in a personalized way for patients with GISTs. RESULTS: The predictive model was built to discriminate high– from low–malignant potential GISTs with an area under the curve (AUC) of 0.882 (95% CI 0.823-0.942) in the training set and 0.920 (95% CI 0.870-0.971) in the validation set. Moreover, the other radiomic model was built to differentiate high– from low–mitotic count GISTs with an AUC of 0.820 (95% CI 0.753-0.887) in the training set and 0.769 (95% CI 0.654-0.883) in the validation set. CONCLUSION: The radiomic models using CE-CT showed a good predictive performance for preoperative risk stratification of GISTs and hold great potential for personalized clinical decision making.
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spelling pubmed-66141152019-07-18 Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors Wang, Chao Li, Hailin Jiaerken, Yeerfan Huang, Peiyu Sun, Lifeng Dong, Fei Huang, Yajing Dong, Di Tian, Jie Zhang, Minming Transl Oncol Original article PURPOSE: To build radiomic prediction models using contrast-enhanced computed tomography (CE-CT) to preoperatively predict malignant potential and mitotic count of gastrointestinal stromal tumors (GISTs). PATIENTS AND METHODS: A total of 333 GISTs patients were retrospectively included in our study. Radiomic features were extracted from the preoperative CE-CT images. According to postoperative pathology, patients were categorized by malignant potential and mitotic count, respectively. The most valuable radiomic features were chosen to build a logistic regression model to predict the malignant potential and a random forest classifier model to predict the mitotic count. The performance of radiomic models was assessed with the receiver operating characteristics curve. Our study further developed a radiomic nomogram to preoperatively predict malignant potential in a personalized way for patients with GISTs. RESULTS: The predictive model was built to discriminate high– from low–malignant potential GISTs with an area under the curve (AUC) of 0.882 (95% CI 0.823-0.942) in the training set and 0.920 (95% CI 0.870-0.971) in the validation set. Moreover, the other radiomic model was built to differentiate high– from low–mitotic count GISTs with an AUC of 0.820 (95% CI 0.753-0.887) in the training set and 0.769 (95% CI 0.654-0.883) in the validation set. CONCLUSION: The radiomic models using CE-CT showed a good predictive performance for preoperative risk stratification of GISTs and hold great potential for personalized clinical decision making. Neoplasia Press 2019-07-04 /pmc/articles/PMC6614115/ /pubmed/31280094 http://dx.doi.org/10.1016/j.tranon.2019.06.005 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Wang, Chao
Li, Hailin
Jiaerken, Yeerfan
Huang, Peiyu
Sun, Lifeng
Dong, Fei
Huang, Yajing
Dong, Di
Tian, Jie
Zhang, Minming
Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors
title Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors
title_full Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors
title_fullStr Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors
title_full_unstemmed Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors
title_short Building CT Radiomics-Based Models for Preoperatively Predicting Malignant Potential and Mitotic Count of Gastrointestinal Stromal Tumors
title_sort building ct radiomics-based models for preoperatively predicting malignant potential and mitotic count of gastrointestinal stromal tumors
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614115/
https://www.ncbi.nlm.nih.gov/pubmed/31280094
http://dx.doi.org/10.1016/j.tranon.2019.06.005
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