Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
BJU Int. 2012 Jun;109(12):1764-9. doi: 10.1111/j.1464-410X.2011.10628.x. Epub 2011 Oct 21.
Study Type - Therapy (case series) Level of Evidence 4 What's known on the subject? and What does the study add? High-grade prostate cancers are associated with poor disease-specific outcomes. A proportion of these tumours produce little PSA. This study demonstrates that among Gleason 8-10 prostate cancers, some of the worst survival outcomes are associated with the lowest PSA levels.
• To assess outcomes of patients with Gleason score 8-10 prostate cancer (CaP) with a low (≤ 2.5 ng/mL) vs higher preoperative serum PSA levels.
• From 1983 to 2003, 5544 patients underwent open radical prostatectomy, of whom 354 had a Gleason 8-10 tumour in the prostatectomy specimen. • Patients were stratified according to preoperative PSA level into four strata: ≤ 2.5 ng/mL (n= 31), 2.6-4 ng/mL (n= 31), 4.1-10 ng/mL (n= 174), and >10 ng/mL (n= 118). • We compared biochemical progression-free survival (PFS), metastasis-free survival (MFS), and cancer-specific survival (CSS) as a function of preoperative PSA level.
• Patients with PSA level ≤ 2.5 ng/mL were more likely to have seminal vesicle invasion (P= 0.003). • On Kaplan-Meier survival analysis, patients with a PSA level ≤ 2.5 ng/mL had proportionately worse outcomes than their counterparts with higher PSA levels. • The 7-year PFS in the PSA ≤ 2.5 ng/mL stratum was lower than those of the PSA 2.6-4 ng/mL and 4-10 ng/mL strata (36% vs 50 and 42%, respectively); however, the lowest 7-year PFS was found in those with a PSA level >10 ng/mL (32%, P= 0.02). • Gleason score 8-10 tumours with a PSA level ≤ 2.5 ng/mL also tended to have the lowest 7-year MFS (75, 93, 89 and 92% for PSA level ≤ 2.5, 2.6-4, 4.1-10 and >10 ng/mL, respectively, P= 0.2) and CSS (81, 100, 94 and 90% for PSA level ≤ 2.5, 2.6-4, 4.1-10 and >10 ng/mL, respectively, P= 0.3), although these differences were not statistically significant. • In the subset with palpable disease, Gleason grade 8-10 disease with PSA level ≤ 2.5 ng/mL also was associated with a worse prognosis.
• In patients with Gleason grade 8-10 disease, a proportion of these tumours are so poorly differentiated that they produce relatively little PSA. • Patients with high-grade, low-PSA tumours had less favourable outcomes than many of those with higher PSA levels.
研究类型 - 治疗(病例系列)证据等级 4 已知内容:高级别前列腺癌与疾病特异性结局不良相关。一部分此类肿瘤产生的 PSA 较少。本研究表明,在 Gleason 8-10 前列腺癌中,一些最差的生存结局与最低 PSA 水平相关。
评估 Gleason 评分 8-10 前列腺癌(CaP)患者中术前 PSA 水平较低(≤2.5ng/ml)与较高(>2.5ng/ml)患者的预后。
1983 年至 2003 年,5544 例患者接受了开放性根治性前列腺切除术,其中 354 例前列腺切除术标本中存在 Gleason 8-10 肿瘤。根据术前 PSA 水平将患者分为四组:≤2.5ng/ml(n=31)、2.6-4ng/ml(n=31)、4.1-10ng/ml(n=174)和>10ng/ml(n=118)。我们比较了不同 PSA 水平下的生化无进展生存率(PFS)、无转移生存率(MFS)和癌症特异性生存率(CSS)。
PSA 水平≤2.5ng/ml 的患者更有可能发生精囊侵犯(P=0.003)。Kaplan-Meier 生存分析显示,PSA 水平≤2.5ng/ml 的患者比 PSA 水平较高的患者预后更差。PSA≤2.5ng/ml 组的 7 年 PFS 低于 PSA 2.6-4ng/ml 和 4-10ng/ml 组(分别为 36%、50%和 42%);然而,PSA 水平>10ng/ml 组的 7 年 PFS 最低(32%,P=0.02)。PSA 水平≤2.5ng/ml 的 Gleason 评分 8-10 肿瘤也倾向于具有最低的 7 年 MFS(PSA 水平分别为≤2.5ng/ml、2.6-4ng/ml、4.1-10ng/ml 和>10ng/ml 的患者为 75%、93%、89%和 92%,P=0.2)和 CSS(PSA 水平分别为≤2.5ng/ml、2.6-4ng/ml、4.1-10ng/ml 和>10ng/ml 的患者为 81%、100%、94%和 90%,P=0.3),尽管这些差异无统计学意义。在可触及疾病的亚组中,PSA 水平≤2.5ng/ml 的 Gleason 分级 8-10 疾病也与预后不良相关。
在 Gleason 分级 8-10 肿瘤患者中,一部分肿瘤分化较差,因此产生的 PSA 较少。高分级、低 PSA 肿瘤患者的预后不如许多 PSA 水平较高的患者。