MRI-Guided Targeted and Systematic Prostate Biopsies as Prognostic Indicators for Prostate Cancer Treatment Decisions

Author:

Abd Ali Furat1,Sievert Karl-Dietrich1,Eisenblaetter Michel2,Titze Barbara3,Hansen Torsten4,Barth Peter J.5,Titze Ulf3ORCID

Affiliation:

1. Bielefeld University, Medical School and University Medical Center OWL, Klinikum Lippe Detmold, Department of Urology, 32756 Detmold, Germany

2. Bielefeld University, Medical School and University Medical Center OWL, Klinikum Lippe Detmold, Department of Diagnostic and Interventional Radiology, 32756 Detmold, Germany

3. Bielefeld University, Medical School and University Medical Center OWL, Department of Pathology, Klinikum Lippe Detmold, 32756 Detmold, Germany

4. MVZ for Histology, Cytology and Molecular Diagnostics Trier GmbH, 54296 Trier, Germany

5. University of Münster, Gerhard-Domagk-Institute of Pathology, Münster University Hospital, 48149 Münster, Germany

Abstract

The standard procedure for the diagnosis of prostate carcinoma involves the collection of 10–12 systematic biopsies (SBx) from both lobes. MRI-guided targeted biopsies (TBx) from suspicious foci increase the detection rates of clinically significant (cs) PCa. We investigated the extent to which the results of the TBx predicted the tumor board treatment decisions. SBx and TBx were acquired from 150 patients. Risk stratifications and recommendations for interventional therapy (prostatectomy and radiotherapy) or active surveillance were established by interdisciplinary tumor boards. We analyzed how often TBx alone were enough to correctly classify the tumors as well as to indicate interventional therapy and how often the findings of SBx were crucial for therapy decisions. A total of 28/39 (72%) favorable risk tumors were detected in TBx, of which 11/26 (42%) very-low-risk tumors were not detected and 8/13 (62%) low-risk tumors were undergraded. A total of 36/44 (82%) intermediate-risk PCa were present in TBx, of which 4 (9%) were underdiagnosed as a favorable risk tumor. A total of 12/13 (92%) high-risk carcinomas were detected and correctly grouped in TBx. The majority of csPCa were identified by the sampling of TBx alone. The tumor size was underestimated in a proportion of ISUP grade 1 tumors. Systematic biopsy sampling is therefore indicated for the next AS follow-up in these cases.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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