Should Targeted Biopsy be Performed in Patients Who Have Only Pi-rads 3 Lesions?


Journal

Archivos espanoles de urologia
ISSN: 0004-0614
Titre abrégé: Arch Esp Urol
Pays: Spain
ID NLM: 0064757

Informations de publication

Date de publication:
Jun 2022
Historique:
entrez: 19 8 2022
pubmed: 20 8 2022
medline: 23 8 2022
Statut: ppublish

Résumé

To determine whether clinical or radiological parameters can predict clinically significant prostate cancer (csPC) in patients with the Prostate Imaging Reporting and Data System (PI-RADS) 3 lesions. Data were obtained from 247 patients with PI-RADS 3 lesions on mpMRI and who had received a software guided transperineal/transrectal MRI/transrectal ultrasonography (MRI/TRUS) fusion prostate biopsy with concomitant standard systematic 12-core biopsy following mpMRI in the prostate cancer and prostate biopsy database of Turkish Urooncology Association, between 2016 and 2020. The cut-off values of clinical parameters were determined using receiver operating characteristic (ROC) curve analysis. Simple and multiple logistic regression analyses were performed to determine the clinical parameters in predicting csPC. A total of 56 patients (22.6%) had prostate cancer, 23 (9.3%) of whom had csPC. In the lesion- based analysis, cancer detection rates (CDRs) of each lesion in targeted biopsy were found to be 6% and 5% for ISUP GG 1 and ISUP GG ≥ 2, respectively. In the patient-based analysis, clinically insignificant CDRs were significantly higher in systematic biopsy compared with targeted biopsy, whereas no significant difference was found in terms of clinically significant CDRs (p = 0.020 and p=0.422, respectively). The cut-off values were determined as 48.3 mL (AUC [95% CI] = 0.68 [0.53-0.82]) for prostate volume, and 0.213 ng/mL/mL (AUC [95% CI] = 0.64 (0.51-0.77]) for PSAD in predicting csPC. In the multiple logistic regression analysis, only PSAD was found to be an independent risk factor in predicting csPC (OR [95% CI]: 3.56 [1.15-10.91], p = 0.024). Since PSAD > 0.20 ng/mL/mL was found to be positive independent risk factor in predicting csPC, in the absence of advanced radiological parameters, PSAD could be used for the biopsy decision in patients with PI-RADS 3 lesions.

Identifiants

pubmed: 35983811
pii: 1659082238563-1239218271
doi: 10.37554/en-j.arch.esp.urol-20210717-3506-26
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

410-415

Auteurs

Murat Yavuz Koparal (MY)

Department of Urology, Recep Tayyip Erdoğan University Training and Research Hospital Rize, Turkey.

Tevfik Sinan Sözen (TS)

Department of Urology, School of Medicine, Gazi University, Ankara, Turkey.

Nejdet Karşiyakali (N)

Department of Urology, School of Medicine, Acıbadem University, İstanbul, Turkey.

Bülent Akdoğan (B)

Department of Urology, School of Medicine, Hacettepe University, Ankara, Turkey.

Haluk Özen (H)

Department of Urology, School of Medicine, Hacettepe University, Ankara, Turkey.

Güven Aslan (G)

Department of Urology, School of Medicine, Dokuz Eylül University, İzmir, Turkey.

Levent Türkeri (L)

Department of Urology, School of Medicine, Acıbadem University, İstanbul, Turkey.

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Classifications MeSH