Evaluating the performance of clinical and radiological data in predicting prostate cancer in prostate imaging reporting and data system version 2.1 category 3 lesions of the peripheral and the transition zones
Purpose To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ). Methods T...
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| Published in: | International urology and nephrology Vol. 54; no. 2; pp. 263 - 271 |
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| Main Authors: | , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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Springer Nature B.V |
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| ISSN: | 0301-1623, 1573-2584, 1573-2584 |
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| Abstract | Purpose
To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ).
Methods
The mpMRI of patients with PIRADSv2.1 3 lesions who had undergone fusion targeted biopsy was reviewed. Morphological pattern, diffusion parameters and vascularisation were evaluated. The radiological/histopathological data of benign and malignant lesions, between the PZ and TZ were compared. Univariate and multivariate analyses were carried out to identify the clinical and radiological data capable of predicting PCa.
Results
One hundred and twenty-three lesions were assessed, 93 (76%) in the PZ and 30 (24%) in the TZ. Of these, 56 (46%) were PCa and 67 (54%) were benign. The majority of the PCas were Grade Group System (GGS) 1 (38%) and GGS 2 (39%); tumours having a GGS ≥ 3 were more frequently in the TZ (
p
= 0.02). Univariate analysis showed a significant correlation between PCa and prostate volume, prostate-specific antigen (PSA) density
,
lesion zone and the apparent diffusion coefficient
.
At multivariate logistic regression PSA density > 0.15 ng/ml/ml {Odds ratio [OR] 2.38;
p
= 0.001} and lesion zone (i.e. TZ OR 7.55) were independent predictors of PCa (all
p
≤ 0.04).
Conclusion
In solitary PIRADSv2.1 3 lesions, the most important predictive factor was the location zone, with a much greater risk for TZ lesions. |
|---|---|
| AbstractList | PurposeTo define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ).MethodsThe mpMRI of patients with PIRADSv2.1 3 lesions who had undergone fusion targeted biopsy was reviewed. Morphological pattern, diffusion parameters and vascularisation were evaluated. The radiological/histopathological data of benign and malignant lesions, between the PZ and TZ were compared. Univariate and multivariate analyses were carried out to identify the clinical and radiological data capable of predicting PCa. ResultsOne hundred and twenty-three lesions were assessed, 93 (76%) in the PZ and 30 (24%) in the TZ. Of these, 56 (46%) were PCa and 67 (54%) were benign. The majority of the PCas were Grade Group System (GGS) 1 (38%) and GGS 2 (39%); tumours having a GGS ≥ 3 were more frequently in the TZ (p = 0.02). Univariate analysis showed a significant correlation between PCa and prostate volume, prostate-specific antigen (PSA) density, lesion zone and the apparent diffusion coefficient. At multivariate logistic regression PSA density > 0.15 ng/ml/ml {Odds ratio [OR] 2.38; p = 0.001} and lesion zone (i.e. TZ OR 7.55) were independent predictors of PCa (all p ≤ 0.04).ConclusionIn solitary PIRADSv2.1 3 lesions, the most important predictive factor was the location zone, with a much greater risk for TZ lesions. To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ).PURPOSETo define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ).The mpMRI of patients with PIRADSv2.1 3 lesions who had undergone fusion targeted biopsy was reviewed. Morphological pattern, diffusion parameters and vascularisation were evaluated. The radiological/histopathological data of benign and malignant lesions, between the PZ and TZ were compared. Univariate and multivariate analyses were carried out to identify the clinical and radiological data capable of predicting PCa.METHODSThe mpMRI of patients with PIRADSv2.1 3 lesions who had undergone fusion targeted biopsy was reviewed. Morphological pattern, diffusion parameters and vascularisation were evaluated. The radiological/histopathological data of benign and malignant lesions, between the PZ and TZ were compared. Univariate and multivariate analyses were carried out to identify the clinical and radiological data capable of predicting PCa.One hundred and twenty-three lesions were assessed, 93 (76%) in the PZ and 30 (24%) in the TZ. Of these, 56 (46%) were PCa and 67 (54%) were benign. The majority of the PCas were Grade Group System (GGS) 1 (38%) and GGS 2 (39%); tumours having a GGS ≥ 3 were more frequently in the TZ (p = 0.02). Univariate analysis showed a significant correlation between PCa and prostate volume, prostate-specific antigen (PSA) density, lesion zone and the apparent diffusion coefficient. At multivariate logistic regression PSA density > 0.15 ng/ml/ml {Odds ratio [OR] 2.38; p = 0.001} and lesion zone (i.e. TZ OR 7.55) were independent predictors of PCa (all p ≤ 0.04).RESULTSOne hundred and twenty-three lesions were assessed, 93 (76%) in the PZ and 30 (24%) in the TZ. Of these, 56 (46%) were PCa and 67 (54%) were benign. The majority of the PCas were Grade Group System (GGS) 1 (38%) and GGS 2 (39%); tumours having a GGS ≥ 3 were more frequently in the TZ (p = 0.02). Univariate analysis showed a significant correlation between PCa and prostate volume, prostate-specific antigen (PSA) density, lesion zone and the apparent diffusion coefficient. At multivariate logistic regression PSA density > 0.15 ng/ml/ml {Odds ratio [OR] 2.38; p = 0.001} and lesion zone (i.e. TZ OR 7.55) were independent predictors of PCa (all p ≤ 0.04).In solitary PIRADSv2.1 3 lesions, the most important predictive factor was the location zone, with a much greater risk for TZ lesions.CONCLUSIONIn solitary PIRADSv2.1 3 lesions, the most important predictive factor was the location zone, with a much greater risk for TZ lesions. Purpose To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ). Methods The mpMRI of patients with PIRADSv2.1 3 lesions who had undergone fusion targeted biopsy was reviewed. Morphological pattern, diffusion parameters and vascularisation were evaluated. The radiological/histopathological data of benign and malignant lesions, between the PZ and TZ were compared. Univariate and multivariate analyses were carried out to identify the clinical and radiological data capable of predicting PCa. Results One hundred and twenty-three lesions were assessed, 93 (76%) in the PZ and 30 (24%) in the TZ. Of these, 56 (46%) were PCa and 67 (54%) were benign. The majority of the PCas were Grade Group System (GGS) 1 (38%) and GGS 2 (39%); tumours having a GGS ≥ 3 were more frequently in the TZ ( p = 0.02). Univariate analysis showed a significant correlation between PCa and prostate volume, prostate-specific antigen (PSA) density , lesion zone and the apparent diffusion coefficient . At multivariate logistic regression PSA density > 0.15 ng/ml/ml {Odds ratio [OR] 2.38; p = 0.001} and lesion zone (i.e. TZ OR 7.55) were independent predictors of PCa (all p ≤ 0.04). Conclusion In solitary PIRADSv2.1 3 lesions, the most important predictive factor was the location zone, with a much greater risk for TZ lesions. To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate imaging reporting and data system version 2.1 (PIRADSv2.1) 3 lesions of the peripheral and the transition zones (PZ and TZ). The mpMRI of patients with PIRADSv2.1 3 lesions who had undergone fusion targeted biopsy was reviewed. Morphological pattern, diffusion parameters and vascularisation were evaluated. The radiological/histopathological data of benign and malignant lesions, between the PZ and TZ were compared. Univariate and multivariate analyses were carried out to identify the clinical and radiological data capable of predicting PCa. One hundred and twenty-three lesions were assessed, 93 (76%) in the PZ and 30 (24%) in the TZ. Of these, 56 (46%) were PCa and 67 (54%) were benign. The majority of the PCas were Grade Group System (GGS) 1 (38%) and GGS 2 (39%); tumours having a GGS ≥ 3 were more frequently in the TZ (p = 0.02). Univariate analysis showed a significant correlation between PCa and prostate volume, prostate-specific antigen (PSA) density, lesion zone and the apparent diffusion coefficient. At multivariate logistic regression PSA density > 0.15 ng/ml/ml {Odds ratio [OR] 2.38; p = 0.001} and lesion zone (i.e. TZ OR 7.55) were independent predictors of PCa (all p ≤ 0.04). In solitary PIRADSv2.1 3 lesions, the most important predictive factor was the location zone, with a much greater risk for TZ lesions. |
| Author | Gaudiano, Caterina Rustici, Arianna Bianchi, Lorenzo Giunchi, Francesca Braccischi, Lorenzo Corcioni, Beniamino Golfieri, Rita Ciccarese, Federica Schiavina, Riccardo Brunocilla, Eugenio Fiorentino, Michelangelo |
| Author_xml | – sequence: 1 givenname: Caterina orcidid: 0000-0002-3849-8428 surname: Gaudiano fullname: Gaudiano, Caterina email: caterina.gaudiano@aosp.bo.it, caterina.gaudiano@gmail.com organization: Department of Radiology, IRCCS Azienda Ospedaliero-Universitaria di Bologna – sequence: 2 givenname: Lorenzo surname: Bianchi fullname: Bianchi, Lorenzo organization: Department of Urology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna – sequence: 3 givenname: Beniamino surname: Corcioni fullname: Corcioni, Beniamino organization: Department of Radiology, IRCCS Azienda Ospedaliero-Universitaria di Bologna – sequence: 4 givenname: Francesca surname: Giunchi fullname: Giunchi, Francesca organization: Department of Pathology, IRCCS Azienda Ospedaliero-Universitaria di Bologna – sequence: 5 givenname: Riccardo surname: Schiavina fullname: Schiavina, Riccardo organization: Department of Urology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna – sequence: 6 givenname: Federica surname: Ciccarese fullname: Ciccarese, Federica organization: Department of Radiology, IRCCS Azienda Ospedaliero-Universitaria di Bologna – sequence: 7 givenname: Lorenzo surname: Braccischi fullname: Braccischi, Lorenzo organization: Department of Radiology, IRCCS Azienda Ospedaliero-Universitaria di Bologna – sequence: 8 givenname: Arianna surname: Rustici fullname: Rustici, Arianna organization: Department of Radiology, IRCCS Azienda Ospedaliero-Universitaria di Bologna – sequence: 9 givenname: Michelangelo surname: Fiorentino fullname: Fiorentino, Michelangelo organization: Department of Pathology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Department of Specialty, Diagnostic and Experimental Medicine, University of Bologna – sequence: 10 givenname: Eugenio surname: Brunocilla fullname: Brunocilla, Eugenio organization: Department of Urology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna – sequence: 11 givenname: Rita surname: Golfieri fullname: Golfieri, Rita organization: Department of Radiology, IRCCS Azienda Ospedaliero-Universitaria di Bologna |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34822065$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_3389_fonc_2023_1082564 crossref_primary_10_1148_radiol_233337 crossref_primary_10_3389_fonc_2022_908956 crossref_primary_10_3390_cancers15133438 crossref_primary_10_1038_s41391_025_00987_4 |
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| Keywords | Multiparametric magnetic resonance imaging Prostate cancer PIRADS version 2.1 PIRADS 3 lesions |
| Language | English |
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To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in... To define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in prostate... PurposeTo define the value of clinical and radiological data, using multiparametric magnetic resonance imaging (mpMRI), to predict prostate cancer (PCa) in... |
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| Title | Evaluating the performance of clinical and radiological data in predicting prostate cancer in prostate imaging reporting and data system version 2.1 category 3 lesions of the peripheral and the transition zones |
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