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Elastic fusion biopsy versus systematic biopsy for prostate cancer detection: Results of a multicentric study on 1,119 patients. / Evaluación de la biopsia de fusión elástica vs. biopsia sistemática para la detección del cáncer de próstata: resultados de un estudio multicéntrico en 1.119 pacientes.
Oderda, M; Marra, G; Albisinni, S; Altobelli, E; Baco, E; Beatrici, V; Dellabella, M; Descotes, J L; Eldred-Evans, D; Fasolis, G; Ferriero, M; Fiard, G; Giacobbe, A; Kumar, P; Lacetera, V; Mozer, P; Muto, G; Papalia, R; Peltier, A; Piechaud, T; Pierangeli, T; Simone, G; Roche, J B; Roupret, M; Gontero, P.
Afiliación
  • Oderda M; Departamento de Ciencias Quirúrgicas, Urología, Universitad de Turín, Turín, Italia; Departamento de Urología, Hospital San Lázaro, Alba, Italia. Electronic address: marco.oderda83@gmail.com.
  • Marra G; Departamento de Ciencias Quirúrgicas, Urología, Universitad de Turín, Turín, Italia.
  • Albisinni S; Departamento de Urología, Hospital Eraste, Universidad Libre de Bruselas, Bruselas, Bélgica.
  • Altobelli E; Departamento de Urología, Campus Biomédico Universidad, Roma, Italia.
  • Baco E; Departamento de Urología, Hospital Universitario de Oslo, Oslo, Noruega.
  • Beatrici V; Departamento de Urología, Azienda Ospedaliera Ospedali Riuniti Marche Nord, Pesaro-Fano, Italia.
  • Dellabella M; Departamento de Urología, INRCA-IRCCS, Ancona, Italia.
  • Descotes JL; Departamento de Urología, Centre Hospitalier Universitaire de Grenoble, Grenoble, Francia.
  • Eldred-Evans D; Departamento de Urología, Hospital Royal Marsden, Londres, Reino Unido.
  • Fasolis G; Departamento de Urología, Hospital San Lázaro, Alba, Italia.
  • Ferriero M; Departamento de Urología, Regina Elena National Cancer Institute, Roma, Italia.
  • Fiard G; Departamento de Urología, Centre Hospitalier Universitaire de Grenoble, Grenoble, Francia.
  • Giacobbe A; Departamento de Urología, Humanitas Gradenigo Hospital, Turín, Italia.
  • Kumar P; Departamento de Urología, Hospital Royal Marsden, Londres, Reino Unido.
  • Lacetera V; Departamento de Urología, Azienda Ospedaliera Ospedali Riuniti Marche Nord, Pesaro-Fano, Italia.
  • Mozer P; Departamento de Urología, Pitié Salpétrière Hospital, Assistance Publique - Hôpitaux de Paris, Universités Paris Sorbonne, París, Francia.
  • Muto G; Departamento de Urología, Humanitas Gradenigo Hospital, Turín, Italia.
  • Papalia R; Departamento de Urología, Campus Biomédico Universidad, Roma, Italia.
  • Peltier A; Departamento de Urología, Instituto Jules Bordet, Universidad Libre de Bruselas, Bruselas, Bélgica.
  • Piechaud T; Departamento de Urología, Clinique Saint Augustin, Burdeos, Francia.
  • Pierangeli T; Unidad de Cáncer de Próstata, INRCA-IRCCS, Ancona, Italia.
  • Simone G; Departamento de Urología, Regina Elena National Cancer Institute, Roma, Italia.
  • Roche JB; Departamento de Urología, Clinique Saint Augustin, Burdeos, Francia.
  • Roupret M; Departamento de Urología, Pitié Salpétrière Hospital, Assistance Publique - Hôpitaux de Paris, Universités Paris Sorbonne, París, Francia.
  • Gontero P; Departamento de Ciencias Quirúrgicas, Urología, Universitad de Turín, Turín, Italia.
Actas Urol Esp (Engl Ed) ; 43(8): 431-438, 2019 Oct.
Article en En, Es | MEDLINE | ID: mdl-31155373
OBJECTIVES: To assess the accuracy of targeted and systematic biopsies for the detection of prostate cancer (PCa) and clinically significant PCa (csPCa) in the everyday practice, evaluating the need for additional systematic biopsies at the time of targeted biopsy. PATIENTS AND METHODS: From our multicentric database gathering data on 2,115 patients who underwent fusion biopsy with Koelis™ system between 2010 and 2017, we selected 1,119 patients who received targeted biopsies (a median of 3 for each target), followed by systematic sampling of the prostate (12 to 14 cores). Overall and clinically significant cancer detection rate (CDR) of Koelis™ fusion biopsies were assessed, comparing target and systematic biopsies. Secondary endpoint was the identification of predictors of PCa detection. RESULTS: The CDR of targeted biopsies only was 48% for all cancers and 33% for csPCa. The performance of additional, systematic prostate sampling improved the CDR of 15% for all cancers and of 12% for csPCa. PCa was detected in 35%, 69%, and 92% of patients with lesions scored as PI-RADS 3, 4 and 5, respectively. Elevated PI-RADS score and positive digital rectal examination were predictors of PCa, whereas biopsy-naïve status was associated with csPCa. CONCLUSION: In the everyday practice target biopsy with Koelis™ achieves a good CDR for all PCa and csPCa, which is significantly improved by subsequent systematic sampling of the prostate. The outstanding outcomes of fusion biopsy are confirmed also in biopsy-naïve patients. Elevated PI-RADS score and positive digital rectal examination are strongly associated with presence of PCa.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Próstata / Neoplasias de la Próstata Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En / Es Revista: Actas Urol Esp (Engl Ed) Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Próstata / Neoplasias de la Próstata Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En / Es Revista: Actas Urol Esp (Engl Ed) Año: 2019 Tipo del documento: Article