Lesion Volume in a Bi- or Multivariate Prediction Model for the Management of PI-RADS v2.1 Score 3 Category Lesions.


Journal

Turkish journal of urology
ISSN: 2149-3235
Titre abrégé: Turk J Urol
Pays: Turkey
ID NLM: 101643563

Informations de publication

Date de publication:
Jul 2022
Historique:
entrez: 1 8 2022
pubmed: 2 8 2022
medline: 2 8 2022
Statut: ppublish

Résumé

This study aimed at improving the discrimination of Prostate Imaging - Reporting and Data System version 2.1 (PI-RADS v2.1) score 3 suspicious prostate cancer lesions using lesion volume evaluation. Two hundred five PI-RADS v2.1 score 3 lesions were submitted to transperineal MRI/TRUS fusion-targeted biopsy. The lesion volumes were estimated on diffusion-weighted imaging sequence and distributed in PI-RADS 3a (LV < 0.5 mL) and PI-RADS 3b (LV ≥ 0.5 mL) subcategories, using a 0.5 mL cutoff value. Data were retrospectively matched with histopathological findings from the biopsy. Assuming that lesions with LV < or ≥ 0.5 mL were respectively not eligible (benign and indolent PCa lesions) or eligible for biopsy (significant PCa lesions), the diagnostic accuracy of lesion volume in determining clinically significant PCa at biopsy was evaluated using a bi- or multivariate model. About 55.1% and 44.9% of lesions were distributed in subcategories 3a and 3b, respectively. The overall PI-RADS score 3 detection rate was 273%. 3.5% (1.95% of total), and 25% (11.7% of total) significant PCa were found in PI-RADS 3a and 3b subcategory, respectively. The method showed 85.2% sensitivity, 61.2% specificity, 25% positive predictive value, and 96.5% negative predictive value and avoided 55.1% of unnecessary biopsies. The diagnostic accuracy in determining significant PCa at biopsy was 73.2% or 86.5% depending on whether lesion volume was used alone or in combination with prostate volume and patient age in a multivariate model. 0.5 mL lesion volume cutoff value significantly discriminates fusion-targeted biopsy need in PI-RADS v2.1 score 3 lesions and its diagnostic accuracy improves when it combines with prostate volume and age in a multivariate model.

Identifiants

pubmed: 35913442
doi: 10.5152/tud.2022.22038
pmc: PMC9612700
doi:

Types de publication

Journal Article

Langues

eng

Pagination

268-277

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Auteurs

Eugenio Martorana (E)

Department of Urology, New Civilian Hospital of Sassuolo, Modena, Italy.

Maria Cristina Aisa (MC)

Division of Gynaecology, Department of Medicine and Surgery, S. Maria della Misericordia Hospital, Perugia University, Perugia, Italy.

Riccardo Grisanti (R)

Department of Urology, New Civilian Hospital of Sassuolo, Modena, Italy.

Nicola Santini (N)

Department of Radiology, New Civilian Hospital of Sassuolo, Modena, Italy.

Giacomo Maria Pirola (GM)

Department of Urology, Usl Toscana Sud Est, San Donato Hospital, Arezzo, Italy.

Alessandro Datti (A)

Division of Biochemistry, Department of Agricultural, Food, and Environmental Sciences, Perugia University, Perugia, Italy.

Sandro Gerli (S)

Division of Gynaecology, Department of Medicine and Surgery, S. Maria della Misericordia Hospital, Perugia University, Perugia, Italy.

Alessandra Bonora (A)

Division of Anaesthesia, Casa di Cura Fogliani, Modena, Italy.

Aldo Burani (A)

Department of Radiology, New Civilian Hospital of Sassuolo, Modena, Italy.

Giovanni Battista Scalera (GB)

Division of Diagnostic Imaging, Department of Medicine and Surgery, S. Maria della Misericordia Hospital, Perugia University, Italy.

Pietro Scialpi (P)

Division of Urology, Portogruaro Hospital, Venice, Italy.

Aldo Di Blasi (A)

Division of Radiology, Tivoli Hospital, Tivoli, Italy.

Michele Scialpi (M)

Division of Radiology 2, Department of Medicine and Surgery, S. Maria della Misericordia Hospital, Perugia University, Perugia, Italy.

Classifications MeSH