Eggener Scott E, Roehl Kimberly A, Smith Norm D, Antenor Jo Ann V, Han Misop, Catalona William J
Department of Urology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
J Urol. 2005 Apr;173(4):1150-5. doi: 10.1097/01.ju.0000155158.79489.48.
Seminal vesicle invasion (SVI) in a radical prostatectomy (RRP) specimen is associated with a guarded prognosis. We evaluated patients with SVI treated in the pre-prostate specific antigen (PSA) (1983 to 1991) and PSA (1992 to 2003) eras.
Of patients with prostate cancer treated with RRP from January 1983 through March 2002, 220 with SVI were evaluated, including 67 in the pre-PSA era and 153 in the PSA era. Postoperative PSA greater than 0.2 ng/ml was considered biochemical evidence of cancer progression. Survival rates were compared using Kaplan-Meier estimates to calculate progression-free, cancer specific and all cause survival. Multivariate Cox proportional hazard models were used to correlate variables with disease progression.
The incidence of SVI in the PSA era was lower than in the pre-PSA era (6.0% vs 10.2%, p = 0.001). To date 124 patients (56%) have had evidence of cancer progression. The 4 and 7-year progression-free, cancer specific and all cause survival rates were significantly higher in men with SVI in the PSA era (p = 0.02). PSA at diagnosis, cancerous surgical margins and higher Gleason score were significantly associated with progression. Neither adjuvant nor salvage radiotherapy appeared to confer a significant progression-free survival benefit.
The incidence of SVI has decreased in the PSA era. Progression-free, cancer specific and all cause survival rates following RRP in patients with SVI have improved in the PSA era. This may reflect earlier detection in this pathological tumor stage and more favorable prognostic factors associated with PSA screening. Adjuvant radiotherapy does not appear to confer any therapeutic benefit. Salvage radiotherapy can lead to durable PSA regressions in a small percent of men, although no long-term survival advantage can be proved.
根治性前列腺切除术(RRP)标本中的精囊侵犯(SVI)与预后不佳相关。我们评估了在前列腺特异性抗原(PSA)时代之前(1983年至1991年)和PSA时代(1992年至2003年)接受治疗的SVI患者。
对1983年1月至2002年3月接受RRP治疗的前列腺癌患者进行评估,其中220例有SVI,包括PSA时代之前的67例和PSA时代的153例。术后PSA大于0.2 ng/ml被视为癌症进展的生化证据。使用Kaplan-Meier估计值比较生存率,以计算无进展生存期、癌症特异性生存期和全因生存期。多变量Cox比例风险模型用于将变量与疾病进展相关联。
PSA时代SVI的发生率低于PSA时代之前(6.0%对10.2%,p = 0.001)。迄今为止,124例患者(56%)有癌症进展的证据。PSA时代有SVI的男性患者4年和7年的无进展生存期、癌症特异性生存期和全因生存率显著更高(p = 0.02)。诊断时的PSA、癌切缘和更高的Gleason评分与进展显著相关。辅助放疗和挽救性放疗似乎均未带来显著的无进展生存获益。
PSA时代SVI的发生率有所下降。PSA时代SVI患者RRP后的无进展生存期、癌症特异性生存期和全因生存率有所改善。这可能反映了在此病理肿瘤阶段的更早发现以及与PSA筛查相关的更有利的预后因素。辅助放疗似乎没有带来任何治疗益处。挽救性放疗可使一小部分男性患者的PSA持久下降,尽管无法证明其有长期生存优势。