Impact on prostate cancer clinical presentation after non-screening policies at a tertiary-care medical center- a retrospective study

Background: In May 2012 the US Preventive Task Force issued a 'D' recommendation against routine PSA-based early detection of prostate cancer. This recommendation was implemented progressively in our health system. The aim of this study is to defne its impact on prostate cancer staging at...

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Detalles Bibliográficos
Autores: Ajami, Tarek, Durruty, Jaime, Mercader Barrull, Clàudia, Rodríguez-Carunchio, Leonardo, Ribal, María José, Alcaraz Asensio, Antonio, Vilaseca, Antoni
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/183873
Acceso en línea:https://hdl.handle.net/2445/183873
Access Level:acceso abierto
Palabra clave:Càncer de pròstata
Cribratge
Prostate cancer
Medical screening
Descripción
Sumario:Background: In May 2012 the US Preventive Task Force issued a 'D' recommendation against routine PSA-based early detection of prostate cancer. This recommendation was implemented progressively in our health system. The aim of this study is to defne its impact on prostate cancer staging at a tertiary care institution. Methods: A retrospective analysis was performed from 2012 until 2015 at a single center. We analyzed the total number of biopsies performed per year and the positive biopsy rate. For those patients with positive biopsies we recorded diagnostic PSA, clinical stage, ISUP grade group, nodal involvement and metastatic status at diagnosis. Results: A total of 1686 biopsies were analyzed. The positive biopsy rate increased from 25% in 2012 to 40% in 2015 (p<0.05). No change in median PSA was noticed (p=0.627). The biopsies detected higher ISUP grades (p=0.000). In addition, newly diagnosed prostate cancer presented a higher clinical stage (p=0.005), higher metastatic rates (p=0.03) and a tendency to higher lymph node involvement although not statistically signifcant (p=0.09). Conclusion: After the 2012 recommendation, patients presented a higher probability of a prostate cancer diagnosis, with a more adverse ISUP group, clinical stage and metastatic disease. These results should be taken into consideration to implement a risk adapted strategy for prostate cancer screening. Keywords: Prostate cancer, Prostate specifc antigen, Prostate cancer screening