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A new nomogram to predict pathologic outcome following radical prostatectomy
Crippa, Alexandre; Srougi, Miguel; Dall'Oglio, Marcos F; Antunes, Alberto A; Leite, Katia R; Nesrallah, Luciano J; Ortiz, Valdemar.
Afiliación
  • Crippa, Alexandre; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
  • Srougi, Miguel; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
  • Dall'Oglio, Marcos F; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
  • Antunes, Alberto A; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
  • Leite, Katia R; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
  • Nesrallah, Luciano J; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
  • Ortiz, Valdemar; Federal University of Sao Paulo. Division of Urology. Sao Paulo. BR
Int. braz. j. urol ; 32(2): 155-164, Mar.-Apr. 2006. tab
Article en En | LILACS | ID: lil-429027
Biblioteca responsable: BR1.1
ABSTRACT

OBJECTIVE:

To develop a preoperative nomogram to predict pathologic outcome in patients submitted to radical prostatectomy for clinical localized prostate cancer. MATERIALS AND

METHODS:

Nine hundred and sixty patients with clinical stage T1 and T2 prostate cancer were evaluated following radical prostatectomy, and 898 were included in the study. Following a multivariate analysis, nomograms were developed incorporating serum PSA, biopsy Gleason score, and percentage of positive biopsy cores in order to predict the risks of extraprostatic tumor extension, and seminal vesicle involvement.

RESULTS:

In univariate analysis there was a significant association between percentage of positive biopsy cores (p < 0.001), serum PSA (p = 0.001) and biopsy Gleason score (p < 0.001) with extraprostatic tumor extension. A similar pathologic outcome was seen among tumors with Gleason score 7, and Gleason score 8 to 10. In multivariate analysis, the 3 preoperative variables showed independent significance to predict tumor extension. This allowed the development of nomogram-1 (using Gleason scores in 3 categories - 2 to 6, 7 and 8 to 10) and nomogram-2 (using Gleason scores in 2 categories - 2 to 6 and 7 to 10) to predict disease extension based on these 3 parameters. In the validation analysis, 87 percent and 91.1 percent of the time the nomograms-1 and 2, correctly predicted the probability of a pathological stage to within 10 percent respectively.

CONCLUSION:

Incorporating percent of positive biopsy cores to a nomogram that includes preoperative serum PSA and biopsy Gleason score, can accurately predict the presence of extraprostatic disease extension in patients with clinical localized prostate cancer.
Asunto(s)
Texto completo: 1 Índice: LILACS Asunto principal: Neoplasias de la Próstata / Antígeno Prostático Específico / Nomogramas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: Int. braz. j. urol Asunto de la revista: UROLOGIA Año: 2006 Tipo del documento: Article
Texto completo: 1 Índice: LILACS Asunto principal: Neoplasias de la Próstata / Antígeno Prostático Específico / Nomogramas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: Int. braz. j. urol Asunto de la revista: UROLOGIA Año: 2006 Tipo del documento: Article