Clinical Validation of IsoPSA™, a Single Parameter, Structure Based Assay for Improved Detection of High Grade Prostate Cancer.


Journal

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

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 28 2 2019
medline: 9 8 2019
entrez: 28 2 2019
Statut: ppublish

Résumé

Current prostate specific antigen markers to detect prostate cancer are limited by low specificity for high grade disease. IsoPSA™ is a blood based, structure focused assay which predicts risk by partitioning the isoforms of prostate specific antigen that are linked to cancer in an aqueous 2-phase reagent system. We validated the clinical performance of this assay for identifying high grade disease in a new contemporary biopsy cohort. We performed a multicenter prospective validation in 271 men scheduled for prostate biopsy at a total of 7 academic and community centers who were enrolled between May 2017 and March 2018. Blood samples were obtained for assay prior to biopsy. The discrimination power of the assay to detect high grade prostate cancer (Gleason 7 or greater) was evaluated by ROC analysis and compared to prior results. Clinical performance was further improved by comparison with multiparametric magnetic resonance imaging-ultrasound vs transrectal ultrasound guided biopsies. The assay AUC was 0.784 for high grade vs low grade cancer/benign histology, which was superior to the AUCs of total prostate specific antigen and percent free prostate specific antigen. If 1,000 patients were biopsied, the assay would have reduced the number of unnecessary biopsies from 705 to 402 (43%) with only 22 missed high grade cancers, of which 7 would have been Gleason sum 4 + 3 or higher. Subset analysis of multiparametric magnetic resonance imaging guided biopsy produced a substantial improvement of the AUC to 0.831. Validation of the structure based IsoPSA assay demonstrated statistical concordance with previously reported results and verified its superior performance vs concentration based prostate specific antigen and the free-to-total prostate specific antigen ratio. The assay improvement in detecting high grade prostate cancer using multiparametric magnetic resonance imaging-ultrasound guided biopsy may help define a new diagnostic paradigm.

Identifiants

pubmed: 30810464
doi: 10.1097/JU.0000000000000185
doi:

Substances chimiques

Protein Isoforms 0
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Multicenter Study Validation Study

Langues

eng

Pagination

1115-1120

Auteurs

Mark Stovsky (M)

Department of Urology, Glickman Urological and Kidney Institute, Cleveland Clinic , Cleveland , Ohio.
Cleveland Diagnostics, Inc. , Cleveland , Ohio.

Eric A Klein (EA)

Department of Urology, Glickman Urological and Kidney Institute, Cleveland Clinic , Cleveland , Ohio.

Arnon Chait (A)

Cleveland Diagnostics, Inc. , Cleveland , Ohio.

Kannan Manickam (K)

Chesapeake Urology Associates , Baltimore , Maryland.

Andrew J Stephenson (AJ)

Department of Urology, Glickman Urological and Kidney Institute, Cleveland Clinic , Cleveland , Ohio.

Mathew Wagner (M)

Kaiser Permanente Northwest , Clackamas , Oregon.

Martin Dineen (M)

Advanced Urology Institute , Daytona Beach , Florida.

Yair Lotan (Y)

University of Texas Southwestern Medical Center , Dallas , Texas.

Alan Partin (A)

The Brady Urological Institute, The Johns Hopkins University , Baltimore , Maryland.

Jack Baniel (J)

Rabin Medical Center , Petah-Tikva , Israel.

Aimee Kestranek (A)

Cleveland Diagnostics, Inc. , Cleveland , Ohio.

Prasad Gawande (P)

Cleveland Diagnostics, Inc. , Cleveland , Ohio.
Cleveland Diagnostics, Inc. , Cleveland , Ohio.

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Classifications MeSH