Added Value of Concomitant Systematic and Fusion Targeted Biopsies for Grade Group Prediction Based on Radical Prostatectomy Final Pathology on Positive Magnetic Resonance Imaging.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
12 2019
Historique:
pubmed: 28 6 2019
medline: 15 11 2019
entrez: 28 6 2019
Statut: ppublish

Résumé

We assessed the added value of concomitant systematic biopsy for final grade group prediction in patients with positive magnetic resonance imaging who were undergoing targeted biopsy. Included in study were 478 consecutive patients with prebiopsy positive multiparametric magnetic resonance imaging and a greater than 10-core systematic biopsy combined with fusion targeted biopsy who underwent radical prostatectomy. The primary end point was the grade group concordance between biopsy and radical prostatectomy pathology according to the biopsy technique. Clinical and biological factors associated with the performance of systematic biopsy were analyzed. Adding systematic biopsy to targeted biopsy modified the d'Amico risk classification toward more intermediate and high risk in 7.8% of cases, mainly from low to intermediate risk with low risk prostate cancer on targeted biopsy in 44.3%. This reclassification was significantly higher in patients with lower prostate specific antigen and with prostate specific antigen density less than 0.20 ng/ml/gm (11.7% vs 2.4%, p <0.001). The concordance rate between biopsy pathology and radical prostatectomy pathology significantly differed between targeted biopsy and targeted biopsy plus systematic biopsy (45.2% and 51.7%, respectively). The upgrading rate in radical prostatectomy specimens decreased by 22% when systematic biopsy was added to targeted biopsy. Patients in whom systematic biopsy did not modify grading were more likely to have pT3-4 and/or pN1 disease on final pathology (56.9% vs 38.3%, p=0.007). Grading concordance between biopsy pathology and radical prostatectomy pathology was improved by adding systematic biopsy in all patient subgroups. Patients with prostate specific antigen density less than 0.20 ng/ml/gm benefited the most from this combined biopsy strategy. Systematic biopsy reclassified a nonnegligible number of cases toward a higher risk category, mainly the low risk cases. Thus, systematic biopsy could modify treatment decision making.

Identifiants

pubmed: 31246548
doi: 10.1097/JU.0000000000000418
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1182-1187

Auteurs

Guillaume Ploussard (G)

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

Jean-Baptiste Beauval (JB)

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

Marine Lesourd (M)

Department of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Department of Urology, Centre Hospitalier Universitaire 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, Centre Hospitalier Universitaire Toulouse, Toulouse, France.

Bernard Malavaud (B)

Department of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Department of Urology, Centre Hospitalier Universitaire Toulouse, Toulouse, France.

Mathieu Roumiguié (M)

Department of Urology, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.
Department of Urology, Centre Hospitalier Universitaire Toulouse, Toulouse, France.

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