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Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI

PURPOSE: The study aimed to construct a predictive model for clinically significant prostate cancer (csPCa) and investigate its clinical efficacy to reduce unnecessary prostate biopsies. METHODS: A total of 847 patients from institute 1 were included in cohort 1 for model development. Cohort 2 inclu...

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Autores principales: Ma, Zengni, Wang, Xinchao, Zhang, Wanchun, Gao, Kaisheng, Wang, Le, Qian, Lixia, Mu, Jingjun, Zheng, Zhongyi, Cao, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990202/
https://www.ncbi.nlm.nih.gov/pubmed/36882854
http://dx.doi.org/10.1186/s12957-023-02959-1
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author Ma, Zengni
Wang, Xinchao
Zhang, Wanchun
Gao, Kaisheng
Wang, Le
Qian, Lixia
Mu, Jingjun
Zheng, Zhongyi
Cao, Xiaoming
author_facet Ma, Zengni
Wang, Xinchao
Zhang, Wanchun
Gao, Kaisheng
Wang, Le
Qian, Lixia
Mu, Jingjun
Zheng, Zhongyi
Cao, Xiaoming
author_sort Ma, Zengni
collection PubMed
description PURPOSE: The study aimed to construct a predictive model for clinically significant prostate cancer (csPCa) and investigate its clinical efficacy to reduce unnecessary prostate biopsies. METHODS: A total of 847 patients from institute 1 were included in cohort 1 for model development. Cohort 2 included a total of 208 patients from institute 2 for external validation of the model. The data obtained were used for retrospective analysis. The results of magnetic resonance imaging were obtained using Prostate Imaging Reporting and Data System version 2.1 (PI-RADS v2.1). Univariate and multivariate analyses were performed to determine significant predictors of csPCa. The diagnostic performances were compared using the receiver operating characteristic (ROC) curve and decision curve analyses. RESULTS: Age, prostate-specific antigen density (PSAD), and PI-RADS v2.1 scores were used as predictors of the model. In the development cohort, the areas under the ROC curve (AUC) for csPCa about age, PSAD, PI-RADS v2.1 scores, and the model were 0.675, 0.823, 0.875, and 0.938, respectively. In the external validation cohort, the AUC values predicted by the four were 0.619, 0.811, 0.863, and 0.914, respectively. Decision curve analysis revealed that the clear net benefit of the model was higher than PI-RADS v2.1 scores and PSAD. The model significantly reduced unnecessary prostate biopsies within the risk threshold of > 10%. CONCLUSIONS: In both internal and external validation, the model constructed by combining age, PSAD, and PI-RADS v2.1 scores exhibited excellent clinical efficacy and can be utilized to reduce unnecessary prostate biopsies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12957-023-02959-1.
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spelling pubmed-99902022023-03-08 Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI Ma, Zengni Wang, Xinchao Zhang, Wanchun Gao, Kaisheng Wang, Le Qian, Lixia Mu, Jingjun Zheng, Zhongyi Cao, Xiaoming World J Surg Oncol Research PURPOSE: The study aimed to construct a predictive model for clinically significant prostate cancer (csPCa) and investigate its clinical efficacy to reduce unnecessary prostate biopsies. METHODS: A total of 847 patients from institute 1 were included in cohort 1 for model development. Cohort 2 included a total of 208 patients from institute 2 for external validation of the model. The data obtained were used for retrospective analysis. The results of magnetic resonance imaging were obtained using Prostate Imaging Reporting and Data System version 2.1 (PI-RADS v2.1). Univariate and multivariate analyses were performed to determine significant predictors of csPCa. The diagnostic performances were compared using the receiver operating characteristic (ROC) curve and decision curve analyses. RESULTS: Age, prostate-specific antigen density (PSAD), and PI-RADS v2.1 scores were used as predictors of the model. In the development cohort, the areas under the ROC curve (AUC) for csPCa about age, PSAD, PI-RADS v2.1 scores, and the model were 0.675, 0.823, 0.875, and 0.938, respectively. In the external validation cohort, the AUC values predicted by the four were 0.619, 0.811, 0.863, and 0.914, respectively. Decision curve analysis revealed that the clear net benefit of the model was higher than PI-RADS v2.1 scores and PSAD. The model significantly reduced unnecessary prostate biopsies within the risk threshold of > 10%. CONCLUSIONS: In both internal and external validation, the model constructed by combining age, PSAD, and PI-RADS v2.1 scores exhibited excellent clinical efficacy and can be utilized to reduce unnecessary prostate biopsies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12957-023-02959-1. BioMed Central 2023-03-07 /pmc/articles/PMC9990202/ /pubmed/36882854 http://dx.doi.org/10.1186/s12957-023-02959-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ma, Zengni
Wang, Xinchao
Zhang, Wanchun
Gao, Kaisheng
Wang, Le
Qian, Lixia
Mu, Jingjun
Zheng, Zhongyi
Cao, Xiaoming
Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI
title Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI
title_full Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI
title_fullStr Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI
title_full_unstemmed Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI
title_short Developing a predictive model for clinically significant prostate cancer by combining age, PSA density, and mpMRI
title_sort developing a predictive model for clinically significant prostate cancer by combining age, psa density, and mpmri
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990202/
https://www.ncbi.nlm.nih.gov/pubmed/36882854
http://dx.doi.org/10.1186/s12957-023-02959-1
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