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The prognostic nomogram for PSA-incongruent low-risk prostate cancer treated by radical prostatectomy.
Wang, Yan; Zhu, Yinjie; Fan, Liancheng; Liu, Jiazhou; Pan, Jiahua; Xue, Wei.
Afiliação
  • Wang Y; Department of Urology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China.
  • Zhu Y; Department of Urology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China.
  • Fan L; Department of Urology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China.
  • Liu J; Department of Urology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China.
  • Pan J; Department of Urology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China. panjiahua@renji.com.
  • Xue W; Department of Urology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China. xuewei@renji.com.
Int Urol Nephrol ; 55(6): 1447-1452, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37017821
ABSTRACT

OBJECTIVE:

To establish a prognostic nomogram for PSA-incongruent low-risk prostate cancer (PCa) patients (Gleason score 6 and clinical stage T2a) at diagnosis and treated with radical prostatectomy (RP), based on clinical and pathological metrics.

METHODS:

In total, 217 patients diagnosed with PCa were included in this study. All patients had a Gleason score of 6 (GS6) in biopsy, had clinical T2a before surgery and were treated with RP. Biochemical progression-free survival (bPFS) was analyzed using the Kaplan-Meier method. Univariate and multivariate analyses were used to determine prognostic factors related to bPFS. A prognostic nomogram was established based on factors that were significant in the multivariate analyses.

RESULTS:

The median bPFS had a significant difference in the subgroup of PSA at diagnosis (' < 10 ng/mL' 71.698 [67.549-75.847] vs '10-20 ng/mL' 71.038 [66.220-75.857] vs ' ≥ 20 ng/mL' 26.746 [12.384-41.108] months [Log Rank P < 0.001]), the subgroup of T stage upgrade (Negative 70.016 [65.846-74.187] vs 'T2b/c' 69.183 [63.544-74.822] vs 'T3/4' 32.235 [11.877-52.593] months [Log Rank P < 0.001]) and the subgroup of Gleason score upgrade (Negative 72.63 [69.096-76.163] vs '3 + 4' 68.393 [62.243-74.543] vs '4 + 3' 41.427 [27.517-55.336] vs ' ≥ 8' 28.291 [7.527-49.055] [Log Rank P < 0.001]). PSA at diagnoses (Hazard Ratio (HR) 1.027, 95% CI 1.015-1.039, P < 0.001), T stage upgrade (HR 2.116, 95% CI 1.083-4.133, P = 0.028), and Gleason score upgrade (HR 2.831, 95% CI 1.892-4.237, P < 0.001) were identified as independent predictors with significance in multivariable Cox regression analysis. A nomogram was established based on these three factors.

CONCLUSIONS:

Our study indicated that PSA-incongruent low-risk PCa patients (PSA with 10-20 ng/mL) had a similar prognosis to those with real low-risk PCa (PSA < 10 ng/mL) in the D' Amico criteria. We also established a nomogram based on three significant prognostic factors, including PSA at diagnosis, T stage upgrade, and Gleason score upgrade, which were associated with clinical outcomes in prostate cancer patients with GS6 and T2a after surgery.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Antígeno Prostático Específico Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Antígeno Prostático Específico Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China