Cargando…
A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort
Selective identification of men with clinically significant prostate cancer (sPC) is a pivotal issue. Development of a risk model for detecting sPC based on the prostate imaging reporting and data system (PI-RADS) for bi-parametric magnetic resonance imaging (bpMRI) and clinical parameters in a Japa...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458280/ https://www.ncbi.nlm.nih.gov/pubmed/34552143 http://dx.doi.org/10.1038/s41598-021-98195-2 |
_version_ | 1784571271671971840 |
---|---|
author | Sakaguchi, Kazushige Hayashida, Michikata Tanaka, Naoto Oka, Suguru Urakami, Shinji |
author_facet | Sakaguchi, Kazushige Hayashida, Michikata Tanaka, Naoto Oka, Suguru Urakami, Shinji |
author_sort | Sakaguchi, Kazushige |
collection | PubMed |
description | Selective identification of men with clinically significant prostate cancer (sPC) is a pivotal issue. Development of a risk model for detecting sPC based on the prostate imaging reporting and data system (PI-RADS) for bi-parametric magnetic resonance imaging (bpMRI) and clinical parameters in a Japanese cohort is expected to prove beneficial. We retrospectively analyzed clinical parameters and bpMRI findings from 773 biopsy-naïve patients between January 2011 and December 2016. A risk model was established using multivariate logistic regression analysis and presented on a nomogram. Discrimination of the risk model was compared using the area under the receiver operating characteristic curve. Statistical differences between the predictive model and clinical parameters were analyzed using DeLong test. sPC was detected in 343 men (44.3%). Multivariate logistic regression analysis to predict sPC revealed age (P = 0.002), log prostate-specific antigen (P < 0.001), prostate volume (P < 0.001) and PI-RADS scores (P < 0.001) as significant contributors to the model. Area under the curve was higher for the risk model (0.862), than for age (0.646), log prostate-specific antigen (0.652), prostate volume (0.697) or imaging score (0.822). DeLong test results also showed that the novel risk model performed significantly better than those parameters (P < 0.05). This novel risk model performed significantly better compared with PI-RADS scores and other parameters alone, and is thus expected to prove beneficial in making decisions regarding biopsy on suspicion of sPC. |
format | Online Article Text |
id | pubmed-8458280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84582802021-09-24 A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort Sakaguchi, Kazushige Hayashida, Michikata Tanaka, Naoto Oka, Suguru Urakami, Shinji Sci Rep Article Selective identification of men with clinically significant prostate cancer (sPC) is a pivotal issue. Development of a risk model for detecting sPC based on the prostate imaging reporting and data system (PI-RADS) for bi-parametric magnetic resonance imaging (bpMRI) and clinical parameters in a Japanese cohort is expected to prove beneficial. We retrospectively analyzed clinical parameters and bpMRI findings from 773 biopsy-naïve patients between January 2011 and December 2016. A risk model was established using multivariate logistic regression analysis and presented on a nomogram. Discrimination of the risk model was compared using the area under the receiver operating characteristic curve. Statistical differences between the predictive model and clinical parameters were analyzed using DeLong test. sPC was detected in 343 men (44.3%). Multivariate logistic regression analysis to predict sPC revealed age (P = 0.002), log prostate-specific antigen (P < 0.001), prostate volume (P < 0.001) and PI-RADS scores (P < 0.001) as significant contributors to the model. Area under the curve was higher for the risk model (0.862), than for age (0.646), log prostate-specific antigen (0.652), prostate volume (0.697) or imaging score (0.822). DeLong test results also showed that the novel risk model performed significantly better than those parameters (P < 0.05). This novel risk model performed significantly better compared with PI-RADS scores and other parameters alone, and is thus expected to prove beneficial in making decisions regarding biopsy on suspicion of sPC. Nature Publishing Group UK 2021-09-22 /pmc/articles/PMC8458280/ /pubmed/34552143 http://dx.doi.org/10.1038/s41598-021-98195-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Sakaguchi, Kazushige Hayashida, Michikata Tanaka, Naoto Oka, Suguru Urakami, Shinji A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort |
title | A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort |
title_full | A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort |
title_fullStr | A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort |
title_full_unstemmed | A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort |
title_short | A risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a Japanese cohort |
title_sort | risk model for detecting clinically significant prostate cancer based on bi-parametric magnetic resonance imaging in a japanese cohort |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458280/ https://www.ncbi.nlm.nih.gov/pubmed/34552143 http://dx.doi.org/10.1038/s41598-021-98195-2 |
work_keys_str_mv | AT sakaguchikazushige ariskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT hayashidamichikata ariskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT tanakanaoto ariskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT okasuguru ariskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT urakamishinji ariskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT sakaguchikazushige riskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT hayashidamichikata riskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT tanakanaoto riskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT okasuguru riskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort AT urakamishinji riskmodelfordetectingclinicallysignificantprostatecancerbasedonbiparametricmagneticresonanceimaginginajapanesecohort |