Impact of MRI and Targeted Biopsies on Eligibility and Disease Reclassification in MRI-positive Candidates for Active Surveillance on Systematic Biopsies.


Journal

Urology
ISSN: 1527-9995
Titre abrégé: Urology
Pays: United States
ID NLM: 0366151

Informations de publication

Date de publication:
03 2020
Historique:
received: 03 06 2019
revised: 21 08 2019
accepted: 09 10 2019
pubmed: 4 1 2020
medline: 13 3 2020
entrez: 4 1 2020
Statut: ppublish

Résumé

To assess the impact of concomitant targeted biopsies (TB) for predicting final disease reclassification in MRI-positive low-risk prostate cancer patients eligible for active surveillance (AS) on systematic biopsies (SB). From a prospective database, we included all prebiopsy MRI-positive men fulfilling AS criteria at diagnosis (Toronto [n = 114], UCSF [n = 82], or PRIAS [n = 60] criteria) on SB. All patients underwent a combination of SB and software-based fusion TB, and an immediate radical prostatectomy. The primary endpoints were the pathologic upgrading and upstaging rates. Biopsy grade group was upgraded to grade group (GG) 2 and to GG≥3 on TB in 65.9%-76.7% and in 12.2-16.7%, respectively. The rate of GG ≥3 in radical prostatectomy specimens varied from 31.6% to 43.3% with no relation between strictest criteria and lower upgrading rates. The proportion of not organ-confined disease (35%-39%) was comparable among the AS cohorts. Negative TB was strongly associated with the absence of final GG ≥3. Tumor grade on TB was significantly correlated with the risk of final GG ≥3 in both Toronto and UCSF cohorts, not in the PRIAS cohort. In the PRIAS cohort, the only independent predictive factor for GG ≥3 disease was the maximal tumor length in any core (P = .034). In MRI-positive patients, the risk of disease reclassification was comparable whatever the SB-based AS criteria used. TB were predictive of final upgrading, with a varied impact according to the AS criteria. SB features remained relevant for reclassification prediction even in case of positive TB. The risk of upstaged disease remains important, approximately one third, and neither TB/SB parameters nor MRI findings could accurately predict it.

Identifiants

pubmed: 31899229
pii: S0090-4295(19)31124-0
doi: 10.1016/j.urology.2019.10.039
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

126-132

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Guillaume Ploussard (G)

Department of Urology, La Croix du Sud Hospital, Quint Fonsegrives, France; Department of Urology, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France. Electronic address: g.ploussard@gmail.com.

Jean-Baptiste Beauval (JB)

Department of Urology, CHU Toulouse, Toulouse, France.

Marine Lesourd (M)

Department of Urology, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France; Department of Urology, CHU Toulouse, Toulouse, France.

Christophe Almeras (C)

Department of Urology, La Croix du Sud Hospital, Quint Fonsegrives, France.

Jacques Assoun (J)

Department of Radiology, La Croix du Sud Hospital, Quint Fonsegrives, France.

Richard Aziza (R)

Department of Radiology, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France.

Jean-Romain Gautier (JR)

Department of Urology, La Croix du Sud Hospital, Quint Fonsegrives, France.

Guillaume Loison (G)

Department of Urology, La Croix du Sud Hospital, Quint Fonsegrives, France.

Daniel Portalez (D)

Department of Radiology, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France.

Ambroise Salin (A)

Department of Urology, La Croix du Sud Hospital, Quint Fonsegrives, France.

Christophe Tollon (C)

Department of Urology, La Croix du Sud Hospital, Quint Fonsegrives, France.

Michel Soulié (M)

Department of Urology, CHU Toulouse, Toulouse, France.

Bernard Malavaud (B)

Department of Urology, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France; Department of Urology, CHU Toulouse, Toulouse, France.

Mathieu Roumiguié (M)

Department of Urology, Institut Universitaire du Cancer Toulouse - Oncopole, Toulouse, France; Department of Urology, CHU Toulouse, Toulouse, France.

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Classifications MeSH