Correlation of mRNA-PCA3 urine levels with the new grading system in prostate cancer.


Journal

Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia
ISSN: 1988-561X
Titre abrégé: Rev Esp Patol
Pays: Spain
ID NLM: 100885154

Informations de publication

Date de publication:
Historique:
received: 24 01 2018
revised: 18 04 2018
accepted: 22 04 2018
entrez: 26 12 2018
pubmed: 26 12 2018
medline: 2 5 2020
Statut: ppublish

Résumé

To evaluate the PCA3 (Prostate Cancer 3 gene) as a tool to improve prostate cancer (PCa) screening and its capability to predict PCa aggressiveness. A retrospective study with data from consecutive patients with suspected PCa seen in the urology department between November 2009 and April 2016 and who were candidates for prostate biopsy. A total of 1038 urine samples were tested in our laboratory with a kit that generated a PCA3 score (s-PCA3). A prostate biopsy was recommended only in those patients with s-PCA3≥35. Associations between variables were analyzed using the R software. In patients with a positive s-PCA3 (44.5%), a subsequent biopsy was recommended. Of a total of 151 biopsies studied, 56.3% yielded a diagnosis of PCa. The probability of a positive biopsy increased as the s-PCA3 increased (p=0.041). The percentage of affected cylinders increased as the s-PCA3 increased (p=0.015). A statistically significant relationship was observed between s-PCA3 and both the Gleason score and the Grade Group (p=0.001 and 0.008, respectively). The best log-linear models and a logistic model confirmed the relationships shown previously with Fisher's exact tests. S-PCA3 may serve as an additional marker to reduce the indication for biopsies and avoid overdiagnosis and overtreatment of patients with suspected PCa. The prognostic significance of s-PCA3 was confirmed, as it was associated with tumor volume and Gleason score. Importantly, to our knowledge this is the first time that an association has been demonstrated between s-PCA3 and the new Grade Group.

Identifiants

pubmed: 30583827
pii: S1699-8855(18)30038-2
doi: 10.1016/j.patol.2018.04.003
pii:
doi:

Substances chimiques

Antigens, Neoplasm 0
RNA, Messenger 0
prostate cancer antigen 3, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20-26

Informations de copyright

Copyright © 2018 Sociedad Española de Anatomía Patológica. Publicado por Elsevier España, S.L.U. All rights reserved.

Auteurs

Natalia Rodon (N)

BIOPAT, Biopatologia Molecular SL, Grup Assistència, Barcelona, Spain. Electronic address: nrodon@biopat.es.

Isabel Trias (I)

BIOPAT, Biopatologia Molecular SL, Grup Assistència, Barcelona, Spain; HISTOPAT Laboratoris, Barcelona, Spain; Hospital de Barcelona, SCIAS, Grup Assistència, Barcelona, Spain.

Montse Verdú (M)

BIOPAT, Biopatologia Molecular SL, Grup Assistència, Barcelona, Spain; HISTOPAT Laboratoris, Barcelona, Spain.

Miquel Calvo (M)

Department of Statistics, Faculty of Biology, Universitat de Barcelona, Barcelona, Spain.

Josep Mª Banus (JM)

ICUN, Institut Català d'Urologia i Nefrologia, Barcelona, Spain.

Xavier Puig (X)

BIOPAT, Biopatologia Molecular SL, Grup Assistència, Barcelona, Spain; HISTOPAT Laboratoris, Barcelona, Spain; Hospital de Barcelona, SCIAS, Grup Assistència, Barcelona, Spain.

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Classifications MeSH