Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD 21231, USA.
BJU Int. 2011 Aug;108(3):378-85. doi: 10.1111/j.1464-410X.2010.09878.x. Epub 2010 Nov 23.
• To describe metastasis-free survival (MFS) and overall survival (OS) among men with prostate-specific antigen (PSA)-recurrent prostate cancer after radical prostatectomy who did not receive additional therapy until metastasis, using a multicentre database capturing a wide ethnic mix.
• A retrospective analysis of the Center for Prostate Disease Research National Database (comprised of five US military hospitals and one civilian centre) was performed for patients with PSA relapse (≥ 0.2 ng/mL) after radical prostatectomy who had no additional therapy until the time of radiographic metastatic disease. • We investigated factors influencing metastasis and all-cause mortality using univariate and multivariate Cox regression analysis.
• There were a total of 346 men who underwent radical prostatectomy between May 1983 and November 2008 and fulfilled the entry criteria. All patients had information on survival and 190 men had information on metastasis. Among patients with survival data (n= 346), 10-year OS was 79% after a median follow-up of 8.6 years from biochemical recurrence. • Among men with metastasis data (n= 190), 10-year MFS was 46% after a median follow-up of 7.5 years. • In Cox regressions, four clinical factors (Gleason score, pathological stage, time to PSA relapse and PSA doubling time), as well as age, were predictive of OS and/or MFS in univariate analysis, although only PSA doubling time (≥ 9 vs 3-8.9 vs <3 months) remained independently predictive of these outcomes in multivariate analysis (P < 0.001).
• This multicentre multi-ethnic dataset shows that OS and MFS can be extensive for men with PSA-recurrent prostate cancer, even in the absence of further therapy before metastasis. • This unique patient cohort, the second largest of its type after the Johns Hopkins cohort, confirms that PSA doubling time is the strongest determinant of OS and MFS in men with PSA-recurrent disease. • Longer follow-up and more events will be required to determine whether other variables may also contribute to these outcomes.
描述接受根治性前列腺切除术(RP)后 PSA 复发的前列腺癌患者在未接受任何辅助治疗直至转移时的无转移生存(MFS)和总生存(OS),该研究使用了一个多中心数据库,该数据库包含了来自不同种族的患者。
对来自前列腺疾病研究国家数据库(由五家美国军事医院和一家民营中心组成)的患者进行了回顾性分析,这些患者在接受 RP 后 PSA 复发(≥0.2ng/ml),且在出现影像学转移疾病之前未接受任何辅助治疗。我们使用单变量和多变量 Cox 回归分析来研究影响转移和全因死亡率的因素。
共有 346 名患者于 1983 年 5 月至 2008 年 11 月期间接受了 RP,并符合入选标准。所有患者均有生存资料,190 名患者有转移资料。在有生存数据的患者(n=346)中,中位随访 8.6 年后,10 年 OS 为 79%。在有转移数据的患者(n=190)中,中位随访 7.5 年后,10 年 MFS 为 46%。在 Cox 回归中,4 个临床因素(Gleason 评分、病理分期、PSA 复发时间和 PSA 倍增时间)以及年龄在单变量分析中是 OS 和/或 MFS 的预测因素,但只有 PSA 倍增时间(≥9 个月比 3-8.9 个月比<3 个月)在多变量分析中是这些结局的独立预测因素(P<0.001)。
该多中心多民族数据集表明,即使在转移前没有进一步的治疗,PSA 复发的前列腺癌患者的 OS 和 MFS 也可能很长。这一独特的患者队列是继约翰霍普金斯队列之后的第二大队列,证实了 PSA 倍增时间是 PSA 复发疾病患者 OS 和 MFS 的最强决定因素。需要更长的随访时间和更多的事件来确定其他变量是否也可能对这些结局产生影响。