Audenet François, Rozet François, Resche-Rigon Matthieu, Bernard Rémy, Ingels Alexandre, Prapotnich Dominique, Sanchez-Salas Rafael, Galiano Marc, Barret Eric, Cathelineau Xavier
Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.
Clin Genitourin Cancer. 2017 Dec;15(6):e907-e913. doi: 10.1016/j.clgc.2017.04.024. Epub 2017 Apr 26.
We intended to analyze the outcomes and predictive factors for underestimating the prostate cancer (PCa) grade group (GG) from prostate biopsies in a large monocentric cohort of patients treated by minimally invasive radical prostatectomy (RP).
Using a monocentric prospectively maintained database, we included 3062 patients who underwent minimally invasive RP between 2006 and 2013. We explored clinicopathologic features and outcomes associated with a GG upgrade from biopsy to RP. Multivariate logistic regression was used to develop and validate a nomogram to predict upgrading for GG1.
Biopsy GG was upgraded after RP in 51.5% of cases. Patients upgraded from GG1 to GG2 or GG3 after RP had a longer time to biochemical recurrence than those with GG2 or GG3 respectively, on both biopsy and RP, but a shorter time to biochemical recurrence than those who remained GG1 after RP (P < .0001). In multivariate analyses, variables predicting upgrading for GG1 PCa were age (P = .0014), abnormal digital rectal examination (P < .0001), prostate-specific antigen density (P < .0001), percentage of positive cores (P < .0001), and body mass index (P = .037). A nomogram was generated and validated internally.
Biopsy grading system is misleading in approximately 50% of cases. Upgrading GG from biopsy to RP may have consequences on clinical outcomes. A nomogram using clinicopathologic features could aid the probability of needing to upgrade GG1 patients at their initial evaluation.
我们旨在分析在接受微创根治性前列腺切除术(RP)治疗的大型单中心患者队列中,前列腺活检低估前列腺癌(PCa)分级组(GG)的结果及预测因素。
利用一个单中心前瞻性维护的数据库,我们纳入了2006年至2013年间接受微创RP的3062例患者。我们探讨了与活检至RP时GG升级相关的临床病理特征和结果。采用多变量逻辑回归来开发和验证一个列线图,以预测GG1的升级情况。
51.5%的病例在RP后活检GG升级。RP后从GG1升级到GG2或GG3的患者,其生化复发时间分别比活检和RP时为GG2或GG3的患者长,但比RP后仍为GG1的患者短(P <.0001)。在多变量分析中,预测GG1 PCa升级的变量有年龄(P =.0014)、直肠指检异常(P <.0001)、前列腺特异性抗原密度(P <.0001)、阳性核心百分比(P <.0001)和体重指数(P =.037)。生成了一个列线图并进行了内部验证。
活检分级系统在大约50%的病例中具有误导性。从活检到RP的GG升级可能会对临床结果产生影响。使用临床病理特征的列线图有助于在初始评估时预测GG1患者升级的可能性。