Repeat MRI during active surveillance: natural history of prostatic lesions and upgrading rates.


Journal

BJU international
ISSN: 1464-410X
Titre abrégé: BJU Int
Pays: England
ID NLM: 100886721

Informations de publication

Date de publication:
04 2022
Historique:
revised: 08 10 2021
received: 09 07 2021
accepted: 12 10 2021
pubmed: 24 10 2021
medline: 16 4 2022
entrez: 23 10 2021
Statut: ppublish

Résumé

To assess upgrading rates in patients on active surveillance (AS) for prostate cancer (PCa) after serial multiparametric magnetic resonance imaging (mpMRI). We conducted a retrospective analysis of 558 patients. Five different criteria for mpMRI progression were used: 1) a Prostate Imaging Reporting and Data System (PI-RADS) score increase; 2) a lesion size increase; 3) an extraprostatic extension score increase; 4) overall mpMRI progression; and 5) the number of criteria met for mpMRI progression (0 vs 1 vs 2-3). In addition, two definitions of PCa upgrading were evaluated: 1) International Society of Urological Pathology Grade Group (ISUP GG) ≥2 with >10% of pattern 4 and 2) ISUP GG ≥ 3. Estimated annual percent changes methodology was used to show the temporal trends of mpMRI progression criteria. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of mpMRI progression criteria were also analysed. Multivariable logistic regression models tested PCa upgrading rates. Lower rates over time for all mpMRI progression criteria were observed. The NPV of serial mpMRI scans ranged from 90.5% to 93.5% (ISUP GG≥2 with >10% of pattern 4 PCa upgrading) and from 98% to 99% (ISUP GG≥3 PCa upgrading), depending on the criteria used for mpMRI progression. A prostate-specific antigen density (PSAD) threshold of 0.15 ng/mL/mL was used to substratify those patients who would be able to skip a prostate biopsy. In multivariable logistic regression models assessing PCa upgrading rates, all five mpMRI progression criteria achieved independent predictor status. During AS, approximately 27% of patients experience mpMRI progression at first repeat MRI. However, the rates of mpMRI progression decrease over time at subsequent mpMRI scans. Patients with stable mpMRI findings and with PSAD < 0.15 ng/mL/mL could safely skip surveillance biopsies. Conversely, patients who experience mpMRI progression should undergo a prostate biopsy.

Identifiants

pubmed: 34687137
doi: 10.1111/bju.15623
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

524-533

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 The Authors BJU International © 2021 BJU International.

Références

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Auteurs

Stefano Luzzago (S)

Department of Urology, IEO European Institute of Oncology, IRCCS, Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Mattia Luca Piccinelli (ML)

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

Francesco A Mistretta (FA)

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

Roberto Bianchi (R)

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

Gabriele Cozzi (G)

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

Ettore Di Trapani (E)

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

Antonio Cioffi (A)

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

Michele Catellani (M)

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

Matteo Fontana (M)

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

Letizia Maria Ippolita Jannello (LMI)

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

Francesco Maria Gerardo Botticelli (FMG)

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

Giulia Marvaso (G)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Department of Radiotherapy, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Sarah Alessi (S)

Division of Radiology, IEO European Institute of Oncology IRCCS, Milan, Italy.

Paola Pricolo (P)

Division of Radiology, IEO European Institute of Oncology IRCCS, Milan, Italy.

Matteo Ferro (M)

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.

Barbara A Jereczek-Fossa (BA)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Department of Radiotherapy, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Nicola Fusco (N)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Department of Pathology, IEO European Institute of Oncology, IRCCS, Milan, Italy.

Giuseppe Petralia (G)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Precision Imaging and Research Unit, Department of Medical Imaging and Radiation Sciences, 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 Hemato-Oncology, University of Milan, Milan, Italy.

Gennaro Musi (G)

Department of Urology, IEO European Institute of Oncology, IRCCS, Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

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