Detection of clinically significant prostate cancer by micro-ultrasound-informed systematic biopsy during MRI/micro-ultrasound fusion biopsy.


Journal

Canadian Urological Association journal = Journal de l'Association des urologues du Canada
ISSN: 1911-6470
Titre abrégé: Can Urol Assoc J
Pays: Canada
ID NLM: 101312644

Informations de publication

Date de publication:
Apr 2023
Historique:
medline: 10 12 2022
pubmed: 10 12 2022
entrez: 9 12 2022
Statut: ppublish

Résumé

High-resolution micro-ultrasound (microUS) is a novel imaging technique that may visualize clinically significant prostate cancer (csPCa), including those missed by magnetic resonance imaging (MRI ), in real time during prostate biopsy. From September 2021 to January 2022, 75 consecutive biopsy-naive men were entered into an observational cohort. All men underwent an MRI /microUS fusion prostate biopsy, completed by a single surgeon using the ExactVU device. At time of biopsy, each biopsy core was given a Prostate Risk Identification using MicroUS (PRI-MUS) score. Anonymized data were entered into a RED Cap database. Cancer detection stratified by Prostate Imaging-Reporting & Data System (PI-RADS ) and PRI-MUS score, and imaging modality was captured. Our primary outcome was the detection rate of csPCa in microUS-informed systematic biopsy cores, taken outside MRI-visible lesions, during MRI /microUS fusion prostate biopsy. A median of three MRI-targeted and 12 microUS-informed systematic cores were taken per patient. MRI /microUS biopsy detected PCa in 84%, with csPCa detected in 52%. Of the 900 microUS-informed systematic cores, 105 cores were PRI-MUS ≥3 and 795 cores were PRI-MUS ≤2. csPCa was detected in 35% of the PRI-MUS ≥3 cores compared to 10% of the PRI-MUS ≤2 cores (p<0.0001). Detection of csPCa varied by core type: 8% of patients were diagnosed by MRI-targeted cores only, 38% were diagnosed by microUS-informed systematic cores only, and 54% were diagnosed by both. MicroUS-informed systematic biopsy may be a useful adjunct to MRI, with PRI-MUS ≥3 systematic cores having a 3.5-fold increased risk of csPCa compared to PRI-MUS ≤2 cores.

Identifiants

pubmed: 36486174
pii: cuaj.8094
doi: 10.5489/cuaj.8094
pmc: PMC10073530
doi:

Types de publication

Journal Article

Langues

eng

Pagination

117-120

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Auteurs

Betty Wang (B)

Division of Urology, Department of Surgery, University of Alberta, Edmonton, AB, Canada.

Stacey Broomfield (S)

Division of Urology, Department of Surgery, University of Alberta, Edmonton, AB, Canada.

Anaïs Medina Martín (AM)

Alberta Prostate Cancer Research Initiative (APCaRI ), Edmonton, AB, Canada.

Patrick Albers (P)

Division of Urology, Department of Surgery, University of Alberta, Edmonton, AB, Canada.

Christopher Fung (C)

Department of Radiology & Diagnostic Imaging, University of Alberta, Edmonton, AB, Canada.

Adam Kinnaird (A)

Division of Urology, Department of Surgery, University of Alberta, Edmonton, AB, Canada.
Alberta Prostate Cancer Research Initiative (APCaRI ), Edmonton, AB, Canada.
Cancer Research Institute of Northern Alberta (CRINA), Edmonton, AB, Canada.
Alberta Centre for Urologic Research and Excellence (ACURE ), Edmonton, AB, Canada.
Department of Oncology, University of Alberta, Edmonton, AB, Canada.

Classifications MeSH