Evaluation of Transperineal Magnetic Resonance Imaging/Ultrasound-Fusion Biopsy Compared to Transrectal Systematic Biopsy in the Prediction of Tumour Aggressiveness in Patients with Previously Negative Biopsy.


Journal

Urologia internationalis
ISSN: 1423-0399
Titre abrégé: Urol Int
Pays: Switzerland
ID NLM: 0417373

Informations de publication

Date de publication:
2019
Historique:
received: 05 07 2018
accepted: 27 07 2018
pubmed: 28 8 2018
medline: 30 3 2019
entrez: 28 8 2018
Statut: ppublish

Résumé

We compared the transperineal MRI/ultrasound-fusion biopsy (fusPbx) to transrectal systematic biopsy (sysPbx) in patients with previously negative biopsy and investigated the prediction of tumour aggressiveness with regard to radical prostatectomy (RP) specimen. A total of 710 patients underwent multiparametric magnetic resonance imaging (mpMRI), which was evaluated in accordance with Prostate Imaging Reporting and Data System (PI-RADS). The maximum PI-RADS (maxPI-RADS) was defined as the highest PI-RADS of all lesions detected in mpMRI. In case of proven prostate cancer (PCa) and performed RP, tumour grading of the biopsy specimen was compared to that of the RP. Significant PCa (csPCa) was defined according to Epstein criteria. Overall, scPCa was detected in 40% of patients. The detection rate of scPCa was 33% for fusPbx and 25% for sysPbx alone (p < 0.005). Patients with a maxPI-RADS ≥3 and a prostate specific antigen (PSA)-density ≥0.2 ng/mL2 harboured more csPCa than those with a PSA-density < 0.2 ng/mL2 (41% [33/81] vs. 20% [48/248]; p < 0.001). Compared to the RP specimen (n = 140), the concordance of tumour grading was 48% (γ = 0.57), 36% (γ = 0.31) and 54% (γ = 0.6) in fusPbx, sysPbx and comPbx, respectively. The combination of fusPbx and sysPbx outperforms both biopsy modalities in patients with re-biopsy. Additionally, the PSA-density may represent a predictor for csPCa in patients with maxPI-RADS ≥3.

Identifiants

pubmed: 30149386
pii: 000492495
doi: 10.1159/000492495
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20-26

Informations de copyright

© 2018 S. Karger AG, Basel.

Auteurs

Angelika Borkowetz (A)

Department of Urology, Technische Universität Dresden, Dresden, Germanyangelika.borkowetz@uniklinikum-dresden.de.

Theresa Renner (T)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Ivan Platzek (I)

Department of Radiology and Interventional Radiology, Technische Universität Dresden, Dresden, Germany.

Marieta Toma (M)

Department of Pathology, Technische Universität Dresden, Dresden, Germany.

Roman Herout (R)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Martin Baunacke (M)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Christer Groeben (C)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Johannes Huber (J)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Michael Laniado (M)

Department of Radiology and Interventional Radiology, Technische Universität Dresden, Dresden, Germany.

Gustavo Baretton (G)

Department of Pathology, Technische Universität Dresden, Dresden, Germany.

Michael Froehner (M)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Stefan Zastrow (S)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

Manfred P Wirth (MP)

Department of Urology, Technische Universität Dresden, Dresden, Germany.

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