Effects of "real life" prostate MRI inter-observer variability on total needle samples and indication for biopsy.


Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
10 2020
Historique:
received: 28 10 2019
revised: 07 03 2020
accepted: 19 03 2020
pubmed: 19 4 2020
medline: 29 6 2021
entrez: 19 4 2020
Statut: ppublish

Résumé

Prostate multiparametric magnetic resonance imaging (mpMRI) improves diagnosis of clinically significant cancer and reduces over-detection of nonsignificant cancer. Disagreement in the interpretation of mpMRI readings is well-known, with a reported discrepancy rate of 10% to 42%. We report the clinical repercussions of this variability on prostate biopsy candidates. Medical records of patients referred from 11 medical centers for MR-guided prostate biopsy (MRGpB) between October, 2017 and January, 2019 were retrospectively analyzed. Patients with at least one prostate imaging reporting and data system (PI-RADS) 3 or greater prostate lesion were selected, and the mpMRI studies (all read by others) were reviewed by our prostate mpMRI reader. Outcomes included changes in PI-RADS score and the subsequent effect on total needle samples and indication for biopsy. Eighty-two patients with 128 lesions were suitable for analysis (mean age 66.5 ± 7.1 years, mean PSA 6.8 ± 8.5 ng/ml). Nine (11%) patients had suspicious rectal exams (T2a). Following our prostate mpMRI reader's imaging revisions, the PI-RADS score was downgraded in 66 (52%) lesions, upgraded in 15 (12%), and unchanged in 47 (37%), leaving a total of 84 suspected lesions (kappa = 0.17). Biopsy was deferred in 22 (27%) patients, and an estimated 136.4 (34.4%) samples were avoided (P = 0.0001 for both). There was a trend toward prostate size to correlate with imaging revision and abortion of biopsy (P = 0.06) while enrollment in active surveillance correlated with proof from such outcome (P = 0.007). These data suggest that high interobserver disagreement in prostate mpMRIs from diverse institutes significantly affects prostate biopsy practice. The clinical consequences of this discord are significant.

Identifiants

pubmed: 32303407
pii: S1078-1439(20)30102-2
doi: 10.1016/j.urolonc.2020.03.015
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

793.e13-793.e18

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Barak Rosenzweig (B)

Department of Urology, Chaim Sheba Medical Center, Ramat Gan, Israel; The Sackler Faculty of Medicine, Tel Aviv University, Tel-Aviv, Israel; The Dr. Pinchas Borenstein Talpiot Medical Leadership Program 2013, Chaim Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel. Electronic address: Barak.rosenzweig@sheba.health.gov.il.

Yael Laitman (Y)

Oncogenetics Unit, Institute of Human Genetics, and Meirav High Risk Clinic, Chaim Sheba Medical Center, Tel-Hashomer, Israel.

Dorit E Zilberman (DE)

Department of Urology, Chaim Sheba Medical Center, Ramat Gan, Israel; The Sackler Faculty of Medicine, Tel Aviv University, Tel-Aviv, Israel.

Orit Raz (O)

Assuta Ashdod University Hospital, Ashdod, Israel.

Jacob Ramon (J)

Department of Urology, Chaim Sheba Medical Center, Ramat Gan, Israel; The Sackler Faculty of Medicine, Tel Aviv University, Tel-Aviv, Israel.

Zohar A Dotan (ZA)

Department of Urology, Chaim Sheba Medical Center, Ramat Gan, Israel; The Sackler Faculty of Medicine, Tel Aviv University, Tel-Aviv, Israel.

Orith Portnoy (O)

The Sackler Faculty of Medicine, Tel Aviv University, Tel-Aviv, Israel; Department of Diagnostic Imaging, Chaim Sheba Medical Center, Ramat Gan, Israel.

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