Department of Urology, University Hospital Frankfurt, Goethe University Frankfurt am Main, Theodor Stern Kai 7, 60596, Frankfurt, Germany.
Department of Urology, University Hospital Frankfurt, Goethe University Frankfurt am Main, Theodor Stern Kai 7, 60596, Frankfurt, Germany.
Clin Genitourin Cancer. 2024 Oct;22(5):102158. doi: 10.1016/j.clgc.2024.102158. Epub 2024 Jul 10.
Metachronous metastatic prostate cancer (mmPCa) patients harbor different characteristics and outcomes, relative to DeNovo metastatic PCa patients. Onset of metastatic disease might be influenced by primary PCa characteristics such as Gleason score (GS) or cancer stage, as well as overall survival (OS) by timing of metastatic onset.
We relied on an institutional tertiary-care database to identify mmPCa patients. Kaplan Meier and Cox Regression models tested for onset of metastases and OS, stratified according to GS, pathological stage and time to mmPCa.
Of 341 mmPCa patients, 8% harbored GS6 versus 41% versus 51% GS7 and GS8-10. Median time to onset of metastatic disease was 79 versus 54 versus 41 months for GS6 versus GS7 versus GS8-10 (P = .01). Moreover, median time to onset of metastases was 64 versus 44 months for pT1-2 versus pT3-4 mmPCa patients undergoing radical prostatectomy (P = .027). In multivariable Cox regression models, higher GS and pT-stage was associated with earlier onset of metastases. Additionally, significant OS differences could be observed for time interval of < 24 versus 24-60 versus 60-120 versus ≥ 120 months between primary PCa diagnosis and onset of mmPCa. Specifically, median OS was 56 versus 69 versus 97 months versus not reached (P < .01) for these categories. In multivariable Cox regression, shorter time to metastatic onset was associated with shorter OS.
Timing of mmPCa is strongly influenced by grading and pT-stage in real-life setting. OS benefits can be observed with longer time interval between primary PCa diagnosis and onset of mmPCa.
与初发转移性前列腺癌(DeNovo metastatic PCa)患者相比,异时转移性前列腺癌(mmPCa)患者具有不同的特征和结局。转移性疾病的发生可能受到原发性前列腺癌特征的影响,如 Gleason 评分(GS)或癌症分期,以及转移性疾病发生的时间对总生存(OS)的影响。
我们依赖于一个机构的三级护理数据库来识别 mmPCa 患者。Kaplan-Meier 和 Cox 回归模型用于检测根据 GS、病理分期和发生 mmPCa 的时间进行的转移发生和 OS。
在 341 例 mmPCa 患者中,8%的患者 GS 为 6,41%的患者 GS 为 7,51%的患者 GS 为 8-10。GS 为 6 组、GS 为 7 组和 GS 为 8-10 组的转移性疾病发生的中位时间分别为 79、54 和 41 个月(P=0.01)。此外,接受根治性前列腺切除术的 pT1-2 与 pT3-4 mmPCa 患者的转移性疾病发生的中位时间分别为 64 和 44 个月(P=0.027)。在多变量 Cox 回归模型中,较高的 GS 和 pT 分期与较早的转移发生相关。此外,在原发性前列腺癌诊断与 mmPCa 发生之间的间隔时间<24、24-60、60-120 和≥120 个月时,可以观察到显著的 OS 差异。具体而言,这些类别的中位 OS 分别为 56、69、97 和未达到(P<0.01)。在多变量 Cox 回归中,转移发生的时间较短与 OS 较短相关。
在真实环境中,mmPCa 的发生时间受分级和 pT 分期的强烈影响。在原发性前列腺癌诊断与 mmPCa 发生之间间隔时间较长的情况下,可以观察到 OS 获益。