Systematic sampling during MRI-US fusion prostate biopsy can overcome errors of targeting-prospective single center experience after 300 cases in first biopsy setting.

MRI-TRUS fusion prostate biopsy Multiparametric magnetic resonance imaging (mpMRI) prostate cancer diagnosis systematic biopsy

Journal

Translational andrology and urology
ISSN: 2223-4691
Titre abrégé: Transl Androl Urol
Pays: China
ID NLM: 101581119

Informations de publication

Date de publication:
Dec 2020
Historique:
entrez: 18 1 2021
pubmed: 19 1 2021
medline: 19 1 2021
Statut: ppublish

Résumé

Multiparametric magnetic resonance imaging (mpMRI) and targeted biopsy have become an integral part of the diagnosis of prostate cancer (PCa), as recommended by the European Association of Urology Guidelines. The aim of the current study was to evaluate the performance of MRI and MRI-transrectal ultrasound (TRUS) fusion prostate biopsy as first biopsy setting in a tertiary center. A cohort of 300 patients was included in the current analysis. All patients presented with clinical or biochemical suspicion of PCa and harbored at least one suspect lesion on mpMRI. MRI-TRUS fusion prostate biopsy, followed by 12 core systematic prostate biopsy were performed by the same operator using a rigid registration system. The mean age of the patients was 64 years (IQR: 58-68.5 years) and the mean PSA was 6.35 ng/mL (IQR: 4.84-9.46 ng/mL). Overall cancer and csPCa diagnosis rates were 47% and 40.66%. Overall PCa/csPCa detection rates were 20.4%/11.1%, 52%/45% and 68.5%/66.7% for PI-RADS lesions 3, 4 and 5 (P<0.001/P<0.0001). Larger lesion diameter and lesion volume were associated with PCa diagnosis (P=0.006 and P=0.001, respectively). MRI-TRUS fusion biopsy missed PCa diagnosis in 37 cases (of whom 48.6% ISUP 1) in comparison with 9 patients missed by systematic biopsy (of whom 11.1% ISUP 1). In terms of csPCa, systematic biopsy missed 77.7% of the tumors located in the anterior and transitional areas. The rate of csPCa was highest when targeted biopsy was associated with systematic biopsy: 86.52% MRI-TRUS fusion prostate biopsy improves the diagnosis of csPCa. The main advantage of an MRI-guided approach is the diagnosis of anterior and transitional area tumors. The best results in terms of csPCa diagnosis are obtained by the combination of MRI-TRUS fusion with systematic biopsy. The systematic biopsy performed during MRI-targeted biopsy could have an important role in overcoming errors of MRI-TRUS fusion systems.

Sections du résumé

BACKGROUND BACKGROUND
Multiparametric magnetic resonance imaging (mpMRI) and targeted biopsy have become an integral part of the diagnosis of prostate cancer (PCa), as recommended by the European Association of Urology Guidelines. The aim of the current study was to evaluate the performance of MRI and MRI-transrectal ultrasound (TRUS) fusion prostate biopsy as first biopsy setting in a tertiary center.
METHODS METHODS
A cohort of 300 patients was included in the current analysis. All patients presented with clinical or biochemical suspicion of PCa and harbored at least one suspect lesion on mpMRI. MRI-TRUS fusion prostate biopsy, followed by 12 core systematic prostate biopsy were performed by the same operator using a rigid registration system.
RESULTS RESULTS
The mean age of the patients was 64 years (IQR: 58-68.5 years) and the mean PSA was 6.35 ng/mL (IQR: 4.84-9.46 ng/mL). Overall cancer and csPCa diagnosis rates were 47% and 40.66%. Overall PCa/csPCa detection rates were 20.4%/11.1%, 52%/45% and 68.5%/66.7% for PI-RADS lesions 3, 4 and 5 (P<0.001/P<0.0001). Larger lesion diameter and lesion volume were associated with PCa diagnosis (P=0.006 and P=0.001, respectively). MRI-TRUS fusion biopsy missed PCa diagnosis in 37 cases (of whom 48.6% ISUP 1) in comparison with 9 patients missed by systematic biopsy (of whom 11.1% ISUP 1). In terms of csPCa, systematic biopsy missed 77.7% of the tumors located in the anterior and transitional areas. The rate of csPCa was highest when targeted biopsy was associated with systematic biopsy: 86.52%
CONCLUSIONS CONCLUSIONS
MRI-TRUS fusion prostate biopsy improves the diagnosis of csPCa. The main advantage of an MRI-guided approach is the diagnosis of anterior and transitional area tumors. The best results in terms of csPCa diagnosis are obtained by the combination of MRI-TRUS fusion with systematic biopsy. The systematic biopsy performed during MRI-targeted biopsy could have an important role in overcoming errors of MRI-TRUS fusion systems.

Identifiants

pubmed: 33457225
doi: 10.21037/tau-20-1001
pii: tau-09-06-2510
pmc: PMC7807351
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2510-2518

Informations de copyright

2020 Translational Andrology and Urology. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau-20-1001). The authors have no conflicts of interest to declare

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Auteurs

Emanuel Cata (E)

Urology Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Urology Department, Municipal Hospital, Cluj Napoca, Romania.

Iulia Andras (I)

Urology Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Urology Department, Municipal Hospital, Cluj Napoca, Romania.

Matteo Ferro (M)

Department of Urology, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Pierre Kadula (P)

Urology Department, Municipal Hospital, Cluj Napoca, Romania.

Daniel Leucuta (D)

Medical Informatics and Biostatistics Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.

Gennaro Musi (G)

Department of Urology, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Deliu-Victor Matei (DV)

Department of Urology, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Ottavio De Cobelli (O)

Department of Urology, IEO European Institute of Oncology, IRCCS, Milan, Italy.
Department of Oncology and Hematology-Oncology, Università degli Studi di Milano, Milan, Italy.

Attila Tamas-Szora (A)

Radiology Department, Municipal Hospital, Cluj Napoca, Romania.

Cosmin Caraiani (C)

Medical Imaging Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.

Andrei Lebovici (A)

Radiology Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.

Flavia Epure (F)

Medical Imaging Department, Medisprof Cancer Center, Cluj Napoca, Romania.

Maria Bungardean (M)

Pathology Department, County Emergency Hospital, Cluj Napoca, Romania.

Radu-Tudor Coman (RT)

Epidemiology Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.

Nicolae Crisan (N)

Urology Department, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Urology Department, Municipal Hospital, Cluj Napoca, Romania.

Classifications MeSH