New strategy for the identification of prostate cancer: The combination of Proclarix and the prostate health index.


Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
11 2022
Historique:
revised: 10 06 2022
received: 21 02 2022
accepted: 11 07 2022
pubmed: 17 8 2022
medline: 24 9 2022
entrez: 16 8 2022
Statut: ppublish

Résumé

Prostate health index (PHI) and, more recently, Proclarix have been proposed as serum biomarkers for prostate cancer (PCa). In this study, we aimed to evaluate Proclarix and PHI for predicting clinically significant prostate cancer (csPCa). Proclarix and PHI were measured using samples of 344 men from two different centers. All patients underwent prostate biopsy, and among those, 188 men with PCa on biopsy had an additional radical prostatectomy (RP). All men had a prostate-specific antigen (PSA) between 2 and 10 ng/ml. Evaluation of area under the curve (AUC) and performance at predefined cut-offs of Proclarix and PHI risk scores as well as the linear combination thereof was performed to predict csPCa. PSA density was used as an independent comparator. The cohort median age and PSA were 65 (interquartile range [IQR]: 60-71) and 5.6 (IQR: 4.3-7.2) ng/ml, respectively. CsPCa was diagnosed in 161 (47%) men based on the RP specimen. ROC analysis showed that Proclarix and PHI accurately predicted csPCa with no significant difference (AUC of 0.79 and 0.76, p = 0.378) but significantly better when compared to PSA density (AUC of 0.66, p < 0.001). When using specific cut-offs, Proclarix (cut-off 10) revealed higher specificity and positive predictive value than PHI (cut-off 27) at similar sensitivities. The combination of Proclarix and PHI provided a significant increase in the AUC (p ≤ 0.007) compared to the individual tests alone and the highest clinical benefit was achieved. Results of this study show that both Proclarix and PHI accurately detect the presence of csPCa. The model combining Proclarix and PHI revealed the synergistic effect and improved the diagnostic performance of the individual tests.

Identifiants

pubmed: 35971798
doi: 10.1002/pros.24422
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1469-1476

Informations de copyright

© 2022 Wiley Periodicals LLC.

Références

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Auteurs

Daniela Terracciano (D)

Department of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.

Evelina La Civita (E)

Department of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.

Alcibiade Athanasiou (A)

Proteomedix AG, Research & Development, Zurich-Schlieren, Switzerland.

Antonietta Liotti (A)

Department of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.

Mariano Fiorenza (M)

Department of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.

Michele Cennamo (M)

Department of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.

Felice Crocetto (F)

Department of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples "Federico II", Naples, Italy.

Pierre Tennstedt (P)

Martini-Klinik, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

Ralph Schiess (R)

Proteomedix AG, Research & Development, Zurich-Schlieren, Switzerland.

Alexander Haese (A)

Martini-Klinik, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

Matteo Ferro (M)

Division of Urology, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Thomas Steuber (T)

Martini-Klinik, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

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