Role of targeted biopsy, perilesional biopsy, random biopsy, and their combination in the detection of clinically significant prostate cancer by mpMRI/transrectal ultrasonography fusion biopsy in confirmatory biopsy during active surveillance program.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
12 Oct 2023
Historique:
received: 10 05 2023
accepted: 28 09 2023
revised: 07 09 2023
medline: 13 10 2023
pubmed: 13 10 2023
entrez: 12 10 2023
Statut: aheadofprint

Résumé

Based on the findings of different trials in biopsy naïve patients, target biopsy (TB) plus random biopsy (RB) during mpMRI-guided transrectal ultrasound fusion biopsy (FB) are often also adopted for the biopsy performed during active surveillance (AS) programs. At the moment, a clear consensus on the extent and modalities of the procedure is lacking. To evaluate the increase in diagnostic accuracy achieved by perilesional biopsy (PL) and different RB schemes during FB performed in AS protocol. We collected prospectively the data of 112 consecutive patients with low- or very-low-risk prostate cancer; positive mpMRI underwent biopsy at a single academic institution in the context of an AS protocol. mpMRI/transrectal US FB with Hitachi RVS system with 3 TB and concurrent transrectal 24-core RB. The diagnostic yield of the different possible biopsy schemes (TB only; TB + 4 perilesional (PL) cores; TB + 12-core RB; TB + 24-core RB) was compared by the McNemar test. Univariable and multivariable regression analyses were adopted to identify predictors of any cancer, Gleason grade group (GGG) ≥2 cancers, and the presence of GGG≥2 cancers in the larger schemes only. The detection rate of GGG ≥2 cancers increased to 30%, 39%, and 49% by adding 4 PL cores, 14, and 24 RB cores, respectively, to TB cores (all p values <0.01). On the whole, TB alone, 14-core RB, and 24-core-RB identified 38%, 47%, and 56% of all the GGG ≥2 cancers. Such figures increased to 62% by adding to TB 4 PL cores, and to 80% by adding 14 RB cores. Most of the differences were observed in PI-RADS 4 lesions. We found that PL biopsy increased the detection rate of GGG ≥2 cancers as compared with TB alone. However, the combination of those cores missed a large percentage of the CS cancers identified with larger RB cores, including a 20% of CS cancers diagnosed only by the combination of TB plus 24-core RB.

Sections du résumé

BACKGROUND BACKGROUND
Based on the findings of different trials in biopsy naïve patients, target biopsy (TB) plus random biopsy (RB) during mpMRI-guided transrectal ultrasound fusion biopsy (FB) are often also adopted for the biopsy performed during active surveillance (AS) programs. At the moment, a clear consensus on the extent and modalities of the procedure is lacking.
OBJECTIVE OBJECTIVE
To evaluate the increase in diagnostic accuracy achieved by perilesional biopsy (PL) and different RB schemes during FB performed in AS protocol.
DESIGN, SETTING, AND PARTICIPANTS METHODS
We collected prospectively the data of 112 consecutive patients with low- or very-low-risk prostate cancer; positive mpMRI underwent biopsy at a single academic institution in the context of an AS protocol.
INTERVENTION(S) METHODS
mpMRI/transrectal US FB with Hitachi RVS system with 3 TB and concurrent transrectal 24-core RB.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS METHODS
The diagnostic yield of the different possible biopsy schemes (TB only; TB + 4 perilesional (PL) cores; TB + 12-core RB; TB + 24-core RB) was compared by the McNemar test. Univariable and multivariable regression analyses were adopted to identify predictors of any cancer, Gleason grade group (GGG) ≥2 cancers, and the presence of GGG≥2 cancers in the larger schemes only.
RESULTS AND LIMITATIONS CONCLUSIONS
The detection rate of GGG ≥2 cancers increased to 30%, 39%, and 49% by adding 4 PL cores, 14, and 24 RB cores, respectively, to TB cores (all p values <0.01). On the whole, TB alone, 14-core RB, and 24-core-RB identified 38%, 47%, and 56% of all the GGG ≥2 cancers. Such figures increased to 62% by adding to TB 4 PL cores, and to 80% by adding 14 RB cores. Most of the differences were observed in PI-RADS 4 lesions.
CONCLUSIONS CONCLUSIONS
We found that PL biopsy increased the detection rate of GGG ≥2 cancers as compared with TB alone. However, the combination of those cores missed a large percentage of the CS cancers identified with larger RB cores, including a 20% of CS cancers diagnosed only by the combination of TB plus 24-core RB.

Identifiants

pubmed: 37828151
doi: 10.1038/s41391-023-00733-8
pii: 10.1038/s41391-023-00733-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Giacomo Novara (G)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy. giacomo.novara@unipd.it.

Fabio Zattoni (F)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Giovanni Zecchini (G)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Alberto Aceti (A)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Anna Pellizzari (A)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Giordana Ferraioli (G)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Claudia Cobacchini (C)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Alessandra Taverna (A)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Francesca Sattin (F)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Filippo Carletti (F)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Giulia La Bombarda (G)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Carmelo Salvino Lacognata (CS)

Radiology Unit, University Hospital of Padua, Padua, Italy.

Alberto Lauro (A)

Radiology Unit, University Hospital of Padua, Padua, Italy.

Marina Gardiman (M)

Surgical Pathology Unit, Department of Medicine, University Hospital of Padua, Padua, Italy.

Alessandro Morlacco (A)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Giovanni Betto (G)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Fabrizio Dal Moro (F)

Department of Surgery, Oncology, and Gastroenterology - Urology Clinic, University of Padua, Padua, Italy.

Classifications MeSH