PI‐RADS in Predicting csPCa: A Comparison Between Academic and Nonacademic Centers
ABSTRACT Introduction The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in th...
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Published in | The Prostate Vol. 85; no. 4; pp. 337 - 343 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.03.2025
John Wiley and Sons Inc |
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Abstract | ABSTRACT
Introduction
The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in the execution, interpretation, and reporting of prostate MRI examinations across centers necessitate greater standardization and accuracy. This study compares the diagnostic efficacy of mpMRI from academic and nonacademic centers in detecting csPCa and identifies factors associated with csPCa detection.
Materials and Methods
Between July 2018 and October 2023, we prospectively followed 810 men at SS. Annunziata Hospital of Chieti who underwent MRI/US fusion biopsies due to elevated prostate‐specific antigen (PSA) and/or abnormal digital rectal examination (DRE). Patients with mpMRI‐documented suspicious lesions classified as PI‐RADS ≥ 3 were included. Patients were divided into two groups based on the source of their mpMRI (academic or nonacademic centers). All biopsies were conducted using the MRI/US fusion technique. Clinical, mpMRI, and pathological data were collected and analyzed. Statistical analyses were performed using R software.
Results
The cohort included 354 patients from academic centers and 456 from nonacademic centers. There were no significant differences in patient demographics, such as age and PSA levels, between the groups. Patients at academic centers were more likely to receive a higher number of elevated PI‐RADS scores compared to those at nonacademic centers (PI‐RADS > 3: 72.6% vs. 62.3%, p = 0.003). Histopathological analysis revealed no significant differences in the ISUP grade distribution between groups. Increased age, PSA levels, and positive DRE were significantly associated with higher odds of detecting csPCa. Median PSA density was significantly higher in patients with csPCa compared to those without csPCa (0.14 vs. 0.11 ng/mL/cm³, p < 0.001). Academic centers exhibited a higher odds ratio for csPCa detection in patients with PI‐RADS scores > 3 compared to nonacademic centers.
Conclusion
Our study highlights significant variability in PI‐RADS score assignments between academic and nonacademic centers, affecting csPCa detection rates. This variability underscores the need for greater standardization in PI‐RADS scoring to reduce disparities and improve diagnostic uniformity across centers. |
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AbstractList | ABSTRACT
Introduction
The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in the execution, interpretation, and reporting of prostate MRI examinations across centers necessitate greater standardization and accuracy. This study compares the diagnostic efficacy of mpMRI from academic and nonacademic centers in detecting csPCa and identifies factors associated with csPCa detection.
Materials and Methods
Between July 2018 and October 2023, we prospectively followed 810 men at SS. Annunziata Hospital of Chieti who underwent MRI/US fusion biopsies due to elevated prostate‐specific antigen (PSA) and/or abnormal digital rectal examination (DRE). Patients with mpMRI‐documented suspicious lesions classified as PI‐RADS ≥ 3 were included. Patients were divided into two groups based on the source of their mpMRI (academic or nonacademic centers). All biopsies were conducted using the MRI/US fusion technique. Clinical, mpMRI, and pathological data were collected and analyzed. Statistical analyses were performed using R software.
Results
The cohort included 354 patients from academic centers and 456 from nonacademic centers. There were no significant differences in patient demographics, such as age and PSA levels, between the groups. Patients at academic centers were more likely to receive a higher number of elevated PI‐RADS scores compared to those at nonacademic centers (PI‐RADS > 3: 72.6% vs. 62.3%, p = 0.003). Histopathological analysis revealed no significant differences in the ISUP grade distribution between groups. Increased age, PSA levels, and positive DRE were significantly associated with higher odds of detecting csPCa. Median PSA density was significantly higher in patients with csPCa compared to those without csPCa (0.14 vs. 0.11 ng/mL/cm³, p < 0.001). Academic centers exhibited a higher odds ratio for csPCa detection in patients with PI‐RADS scores > 3 compared to nonacademic centers.
Conclusion
Our study highlights significant variability in PI‐RADS score assignments between academic and nonacademic centers, affecting csPCa detection rates. This variability underscores the need for greater standardization in PI‐RADS scoring to reduce disparities and improve diagnostic uniformity across centers. The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in the execution, interpretation, and reporting of prostate MRI examinations across centers necessitate greater standardization and accuracy. This study compares the diagnostic efficacy of mpMRI from academic and nonacademic centers in detecting csPCa and identifies factors associated with csPCa detection. Between July 2018 and October 2023, we prospectively followed 810 men at SS. Annunziata Hospital of Chieti who underwent MRI/US fusion biopsies due to elevated prostate-specific antigen (PSA) and/or abnormal digital rectal examination (DRE). Patients with mpMRI-documented suspicious lesions classified as PI-RADS ≥ 3 were included. Patients were divided into two groups based on the source of their mpMRI (academic or nonacademic centers). All biopsies were conducted using the MRI/US fusion technique. Clinical, mpMRI, and pathological data were collected and analyzed. Statistical analyses were performed using R software. The cohort included 354 patients from academic centers and 456 from nonacademic centers. There were no significant differences in patient demographics, such as age and PSA levels, between the groups. Patients at academic centers were more likely to receive a higher number of elevated PI-RADS scores compared to those at nonacademic centers (PI-RADS > 3: 72.6% vs. 62.3%, p = 0.003). Histopathological analysis revealed no significant differences in the ISUP grade distribution between groups. Increased age, PSA levels, and positive DRE were significantly associated with higher odds of detecting csPCa. Median PSA density was significantly higher in patients with csPCa compared to those without csPCa (0.14 vs. 0.11 ng/mL/cm³, p < 0.001). Academic centers exhibited a higher odds ratio for csPCa detection in patients with PI-RADS scores > 3 compared to nonacademic centers. Our study highlights significant variability in PI-RADS score assignments between academic and nonacademic centers, affecting csPCa detection rates. This variability underscores the need for greater standardization in PI-RADS scoring to reduce disparities and improve diagnostic uniformity across centers. IntroductionThe introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in the execution, interpretation, and reporting of prostate MRI examinations across centers necessitate greater standardization and accuracy. This study compares the diagnostic efficacy of mpMRI from academic and nonacademic centers in detecting csPCa and identifies factors associated with csPCa detection.Materials and MethodsBetween July 2018 and October 2023, we prospectively followed 810 men at SS. Annunziata Hospital of Chieti who underwent MRI/US fusion biopsies due to elevated prostate‐specific antigen (PSA) and/or abnormal digital rectal examination (DRE). Patients with mpMRI‐documented suspicious lesions classified as PI‐RADS ≥ 3 were included. Patients were divided into two groups based on the source of their mpMRI (academic or nonacademic centers). All biopsies were conducted using the MRI/US fusion technique. Clinical, mpMRI, and pathological data were collected and analyzed. Statistical analyses were performed using R software.ResultsThe cohort included 354 patients from academic centers and 456 from nonacademic centers. There were no significant differences in patient demographics, such as age and PSA levels, between the groups. Patients at academic centers were more likely to receive a higher number of elevated PI‐RADS scores compared to those at nonacademic centers (PI‐RADS > 3: 72.6% vs. 62.3%, p = 0.003). Histopathological analysis revealed no significant differences in the ISUP grade distribution between groups. Increased age, PSA levels, and positive DRE were significantly associated with higher odds of detecting csPCa. Median PSA density was significantly higher in patients with csPCa compared to those without csPCa (0.14 vs. 0.11 ng/mL/cm³, p < 0.001). Academic centers exhibited a higher odds ratio for csPCa detection in patients with PI‐RADS scores > 3 compared to nonacademic centers.ConclusionOur study highlights significant variability in PI‐RADS score assignments between academic and nonacademic centers, affecting csPCa detection rates. This variability underscores the need for greater standardization in PI‐RADS scoring to reduce disparities and improve diagnostic uniformity across centers. The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in the execution, interpretation, and reporting of prostate MRI examinations across centers necessitate greater standardization and accuracy. This study compares the diagnostic efficacy of mpMRI from academic and nonacademic centers in detecting csPCa and identifies factors associated with csPCa detection.INTRODUCTIONThe introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization of clinically significant prostate cancer (csPCa) and guiding targeted biopsies. However, significant disparities in the execution, interpretation, and reporting of prostate MRI examinations across centers necessitate greater standardization and accuracy. This study compares the diagnostic efficacy of mpMRI from academic and nonacademic centers in detecting csPCa and identifies factors associated with csPCa detection.Between July 2018 and October 2023, we prospectively followed 810 men at SS. Annunziata Hospital of Chieti who underwent MRI/US fusion biopsies due to elevated prostate-specific antigen (PSA) and/or abnormal digital rectal examination (DRE). Patients with mpMRI-documented suspicious lesions classified as PI-RADS ≥ 3 were included. Patients were divided into two groups based on the source of their mpMRI (academic or nonacademic centers). All biopsies were conducted using the MRI/US fusion technique. Clinical, mpMRI, and pathological data were collected and analyzed. Statistical analyses were performed using R software.MATERIALS AND METHODSBetween July 2018 and October 2023, we prospectively followed 810 men at SS. Annunziata Hospital of Chieti who underwent MRI/US fusion biopsies due to elevated prostate-specific antigen (PSA) and/or abnormal digital rectal examination (DRE). Patients with mpMRI-documented suspicious lesions classified as PI-RADS ≥ 3 were included. Patients were divided into two groups based on the source of their mpMRI (academic or nonacademic centers). All biopsies were conducted using the MRI/US fusion technique. Clinical, mpMRI, and pathological data were collected and analyzed. Statistical analyses were performed using R software.The cohort included 354 patients from academic centers and 456 from nonacademic centers. There were no significant differences in patient demographics, such as age and PSA levels, between the groups. Patients at academic centers were more likely to receive a higher number of elevated PI-RADS scores compared to those at nonacademic centers (PI-RADS > 3: 72.6% vs. 62.3%, p = 0.003). Histopathological analysis revealed no significant differences in the ISUP grade distribution between groups. Increased age, PSA levels, and positive DRE were significantly associated with higher odds of detecting csPCa. Median PSA density was significantly higher in patients with csPCa compared to those without csPCa (0.14 vs. 0.11 ng/mL/cm³, p < 0.001). Academic centers exhibited a higher odds ratio for csPCa detection in patients with PI-RADS scores > 3 compared to nonacademic centers.RESULTSThe cohort included 354 patients from academic centers and 456 from nonacademic centers. There were no significant differences in patient demographics, such as age and PSA levels, between the groups. Patients at academic centers were more likely to receive a higher number of elevated PI-RADS scores compared to those at nonacademic centers (PI-RADS > 3: 72.6% vs. 62.3%, p = 0.003). Histopathological analysis revealed no significant differences in the ISUP grade distribution between groups. Increased age, PSA levels, and positive DRE were significantly associated with higher odds of detecting csPCa. Median PSA density was significantly higher in patients with csPCa compared to those without csPCa (0.14 vs. 0.11 ng/mL/cm³, p < 0.001). Academic centers exhibited a higher odds ratio for csPCa detection in patients with PI-RADS scores > 3 compared to nonacademic centers.Our study highlights significant variability in PI-RADS score assignments between academic and nonacademic centers, affecting csPCa detection rates. This variability underscores the need for greater standardization in PI-RADS scoring to reduce disparities and improve diagnostic uniformity across centers.CONCLUSIONOur study highlights significant variability in PI-RADS score assignments between academic and nonacademic centers, affecting csPCa detection rates. This variability underscores the need for greater standardization in PI-RADS scoring to reduce disparities and improve diagnostic uniformity across centers. |
Author | Berardinelli, Francesco Nicola, Marta Litterio, Giulio Pizzi, Andrea D. Marchioni, Michele De Palma, Antonio D'Angelo, Emanuela Castellan, Pietro Schips, Luigi Porreca, Annamaria Ferretti, Simone Orsini, Angelo Ciavarella, Davide |
AuthorAffiliation | 5 ITAB Institute for Advanced Biomedical Technologies Gabriele d'Annunzio University of Chieti Chieti Italy 2 Department of Medical Oral Science and Biotechnology G. d'Annunzio University Chieti Italy 3 Department of Urology Universita degli Studi Gabriele d'Annunzio Chieti Pescara Dipartimento di Scienze Mediche Orali e Biotecnologiche Chieti Italy 4 Department of Innovative Technologies in Medicine and Dentistry G. D'Annunzio University Chieti Italy 6 Diagnostic Molecular Pathology, Unit of Anatomic Pathology, SS Annunziata Hospital Chieti Italy 1 Urology Unit, Department of Medical, Oral and Biotechnological Sciences ‘G. d'Annunzio University’ Chieti Italy |
AuthorAffiliation_xml | – name: 6 Diagnostic Molecular Pathology, Unit of Anatomic Pathology, SS Annunziata Hospital Chieti Italy – name: 2 Department of Medical Oral Science and Biotechnology G. d'Annunzio University Chieti Italy – name: 1 Urology Unit, Department of Medical, Oral and Biotechnological Sciences ‘G. d'Annunzio University’ Chieti Italy – name: 5 ITAB Institute for Advanced Biomedical Technologies Gabriele d'Annunzio University of Chieti Chieti Italy – name: 3 Department of Urology Universita degli Studi Gabriele d'Annunzio Chieti Pescara Dipartimento di Scienze Mediche Orali e Biotecnologiche Chieti Italy – name: 4 Department of Innovative Technologies in Medicine and Dentistry G. D'Annunzio University Chieti Italy |
Author_xml | – sequence: 1 givenname: Angelo orcidid: 0009-0009-9372-5847 surname: Orsini fullname: Orsini, Angelo organization: ‘G. d'Annunzio University’ – sequence: 2 givenname: Simone surname: Ferretti fullname: Ferretti, Simone organization: ‘G. d'Annunzio University’ – sequence: 3 givenname: Annamaria surname: Porreca fullname: Porreca, Annamaria organization: G. d'Annunzio University – sequence: 4 givenname: Pietro surname: Castellan fullname: Castellan, Pietro organization: Universita degli Studi Gabriele d'Annunzio Chieti Pescara Dipartimento di Scienze Mediche Orali e Biotecnologiche – sequence: 5 givenname: Giulio surname: Litterio fullname: Litterio, Giulio organization: ‘G. d'Annunzio University’ – sequence: 6 givenname: Davide surname: Ciavarella fullname: Ciavarella, Davide organization: ‘G. d'Annunzio University’ – sequence: 7 givenname: Antonio surname: De Palma fullname: De Palma, Antonio organization: ‘G. d'Annunzio University’ – sequence: 8 givenname: Francesco surname: Berardinelli fullname: Berardinelli, Francesco organization: Universita degli Studi Gabriele d'Annunzio Chieti Pescara Dipartimento di Scienze Mediche Orali e Biotecnologiche – sequence: 9 givenname: Andrea D. surname: Pizzi fullname: Pizzi, Andrea D. organization: Gabriele d'Annunzio University of Chieti – sequence: 10 givenname: Emanuela surname: D'Angelo fullname: D'Angelo, Emanuela organization: Diagnostic Molecular Pathology, Unit of Anatomic Pathology, SS Annunziata Hospital – sequence: 11 givenname: Marta surname: Nicola fullname: Nicola, Marta organization: G. d'Annunzio University – sequence: 12 givenname: Luigi surname: Schips fullname: Schips, Luigi organization: Universita degli Studi Gabriele d'Annunzio Chieti Pescara Dipartimento di Scienze Mediche Orali e Biotecnologiche – sequence: 13 givenname: Michele orcidid: 0000-0002-1702-4127 surname: Marchioni fullname: Marchioni, Michele email: mic.marchioni@gmail.com organization: Universita degli Studi Gabriele d'Annunzio Chieti Pescara Dipartimento di Scienze Mediche Orali e Biotecnologiche |
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Introduction
The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis,... The introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the localization... IntroductionThe introduction of multiparametric prostate magnetic resonance imaging (mpMRI) has revolutionized prostate cancer (PCa) diagnosis, enhancing the... |
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SubjectTerms | academic Academic Medical Centers - statistics & numerical data Age composition Aged Biopsy clinically significant prostate cancer csPCa Humans Image-Guided Biopsy - methods Localization Magnetic resonance imaging Male Middle Aged mpMRI Multiparametric Magnetic Resonance Imaging - methods Multiparametric Magnetic Resonance Imaging - standards nonacademic Original Patients PIRADS Prospective Studies Prostate - diagnostic imaging Prostate - pathology Prostate cancer Prostate-Specific Antigen - blood Prostatic Neoplasms - diagnosis Prostatic Neoplasms - diagnostic imaging Prostatic Neoplasms - pathology Standardization Statistical analysis |
Title | PI‐RADS in Predicting csPCa: A Comparison Between Academic and Nonacademic Centers |
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