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Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features
BACKGROUND: To construct a model based on magnetic resonance imaging (MRI) features and histological and clinical variables for the prediction of pathology-detected extracapsular extension (pECE) in patients with prostate cancer (PCa). METHODS: We performed a prospective 3 T MRI study comparing the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784252/ https://www.ncbi.nlm.nih.gov/pubmed/36550525 http://dx.doi.org/10.1186/s40644-022-00509-8 |
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author | Guerra, Adalgisa Alves, Filipe Caseiro Maes, Kris Joniau, Steven Cassis, João Maio, Rui Cravo, Marília Mouriño, Helena |
author_facet | Guerra, Adalgisa Alves, Filipe Caseiro Maes, Kris Joniau, Steven Cassis, João Maio, Rui Cravo, Marília Mouriño, Helena |
author_sort | Guerra, Adalgisa |
collection | PubMed |
description | BACKGROUND: To construct a model based on magnetic resonance imaging (MRI) features and histological and clinical variables for the prediction of pathology-detected extracapsular extension (pECE) in patients with prostate cancer (PCa). METHODS: We performed a prospective 3 T MRI study comparing the clinical and MRI data on pECE obtained from patients treated using robotic-assisted radical prostatectomy (RARP) at our institution. The covariates under consideration were prostate-specific antigen (PSA) levels, the patient’s age, prostate volume, and MRI interpretative features for predicting pECE based on the Prostate Imaging–Reporting and Data System (PI-RADS) version 2.0 (v2), as well as tumor capsular contact length (TCCL), length of the index lesion, and prostate biopsy Gleason score (GS). Univariable and multivariable logistic regression models were applied to explore the statistical associations and construct the model. We also recruited an additional set of participants—which included 59 patients from external institutions—to validate the model. RESULTS: The study participants included 184 patients who had undergone RARP at our institution, 26% of whom were pECE+ (i.e., pECE positive). Significant predictors of pECE+ were TCCL, capsular disruption, measurable ECE on MRI, and a GS of ≥7(4 + 3) on a prostate biopsy. The strongest predictor of pECE+ is measurable ECE on MRI, and in its absence, a combination of TCCL and prostate biopsy GS was significantly effective for detecting the patient’s risk of being pECE+. Our predictive model showed a satisfactory performance at distinguishing between patients with pECE+ and patients with pECE−, with an area under the ROC curve (AUC) of 0.90 (86.0–95.8%), high sensitivity (86%), and moderate specificity (70%). CONCLUSIONS: Our predictive model, based on consistent MRI features (i.e., measurable ECE and TCCL) and a prostate biopsy GS, has satisfactory performance and sufficiently high sensitivity for predicting pECE+. Hence, the model could be a valuable tool for surgeons planning preoperative nerve sparing, as it would reduce positive surgical margins. |
format | Online Article Text |
id | pubmed-9784252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97842522022-12-24 Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features Guerra, Adalgisa Alves, Filipe Caseiro Maes, Kris Joniau, Steven Cassis, João Maio, Rui Cravo, Marília Mouriño, Helena Cancer Imaging Research Article BACKGROUND: To construct a model based on magnetic resonance imaging (MRI) features and histological and clinical variables for the prediction of pathology-detected extracapsular extension (pECE) in patients with prostate cancer (PCa). METHODS: We performed a prospective 3 T MRI study comparing the clinical and MRI data on pECE obtained from patients treated using robotic-assisted radical prostatectomy (RARP) at our institution. The covariates under consideration were prostate-specific antigen (PSA) levels, the patient’s age, prostate volume, and MRI interpretative features for predicting pECE based on the Prostate Imaging–Reporting and Data System (PI-RADS) version 2.0 (v2), as well as tumor capsular contact length (TCCL), length of the index lesion, and prostate biopsy Gleason score (GS). Univariable and multivariable logistic regression models were applied to explore the statistical associations and construct the model. We also recruited an additional set of participants—which included 59 patients from external institutions—to validate the model. RESULTS: The study participants included 184 patients who had undergone RARP at our institution, 26% of whom were pECE+ (i.e., pECE positive). Significant predictors of pECE+ were TCCL, capsular disruption, measurable ECE on MRI, and a GS of ≥7(4 + 3) on a prostate biopsy. The strongest predictor of pECE+ is measurable ECE on MRI, and in its absence, a combination of TCCL and prostate biopsy GS was significantly effective for detecting the patient’s risk of being pECE+. Our predictive model showed a satisfactory performance at distinguishing between patients with pECE+ and patients with pECE−, with an area under the ROC curve (AUC) of 0.90 (86.0–95.8%), high sensitivity (86%), and moderate specificity (70%). CONCLUSIONS: Our predictive model, based on consistent MRI features (i.e., measurable ECE and TCCL) and a prostate biopsy GS, has satisfactory performance and sufficiently high sensitivity for predicting pECE+. Hence, the model could be a valuable tool for surgeons planning preoperative nerve sparing, as it would reduce positive surgical margins. BioMed Central 2022-12-23 /pmc/articles/PMC9784252/ /pubmed/36550525 http://dx.doi.org/10.1186/s40644-022-00509-8 Text en © The Author(s) 2022 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 Article Guerra, Adalgisa Alves, Filipe Caseiro Maes, Kris Joniau, Steven Cassis, João Maio, Rui Cravo, Marília Mouriño, Helena Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features |
title | Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features |
title_full | Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features |
title_fullStr | Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features |
title_full_unstemmed | Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features |
title_short | Early biomarkers of extracapsular extension of prostate cancer using MRI-derived semantic features |
title_sort | early biomarkers of extracapsular extension of prostate cancer using mri-derived semantic features |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9784252/ https://www.ncbi.nlm.nih.gov/pubmed/36550525 http://dx.doi.org/10.1186/s40644-022-00509-8 |
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