Radiation Oncology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Ann Surg Oncol. 2011 Oct;18(10):2980-7. doi: 10.1245/s10434-011-1660-0. Epub 2011 Mar 23.
The optimal management of patients with clinically localized prostate carcinoma remains undefined due in part to the absence of well-designed, randomized trials.
This retrospective study comprised 505 patients diagnosed with low- or intermediate- risk prostate cancer in 1998-2005 and treated at Hospital Gregorio Marañón (Spain) with radical prostatectomy (RP) or external-beam radiotherapy (EBRT). No adjuvant therapy was administered. Biochemical relapse was defined as a prostate-specific antigen (PSA) level ≥0.4 ng/ml for RP cases and nadir + 2 for EBRT cases. RP was performed in 271 patients (53.6%) and EBRT in 234 patients (46.4%). The median follow-up was 60 months. The analysis end point was to compare the biochemical recurrence-free survival (bRFS) between the two groups.
The 5-year bRFS rates for RP and EBRT were 79 ± 2% and 86 ± 2%, respectively (P = 0.48). Multivariate analysis indicated that initial PSA (P = 0.00), perineural invasion in the biopsy specimen (P = 0.00), Gleason score (P = 0.04), EBRT dose (P = 0.02), and positive margins (P = 0.00) were independent predictors of relapse. A decision tree model was constructed with these variables. In the EBRT cohort, a nadir PSA of <0.3 ng/ml was associated with the best 5-year bRFS (96.6 vs. 56.5% if nadir PSA > 1.3 ng/ml). Late biochemical failure (>5 years) was more frequent in the RT group and with low-dose EBRT (≤72 Gy).
The biochemical failure rates were similar between PR and EBRT in low- and intermediate-risk subgroups. Outcome was determined by classic pre-treatment features, perineural invasion, low-dose EBRT (≤72 Gy), and nadir PSA value in the RT cohort.
由于缺乏精心设计的随机试验,临床上局限性前列腺癌患者的最佳治疗方法仍不明确。
本回顾性研究纳入了 1998 年至 2005 年间在西班牙格雷戈里奥·马拉尼昂医院诊断为低危或中危前列腺癌的 505 例患者,这些患者接受了根治性前列腺切除术(RP)或外照射放疗(EBRT)。未进行辅助治疗。生化复发定义为前列腺特异性抗原(PSA)水平≥0.4ng/ml(RP 病例)和 nadir+2(EBRT 病例)。271 例患者(53.6%)接受 RP 治疗,234 例患者(46.4%)接受 EBRT 治疗。中位随访时间为 60 个月。分析终点为比较两组患者的生化无复发生存率(bRFS)。
RP 和 EBRT 的 5 年 bRFS 率分别为 79±2%和 86±2%(P=0.48)。多因素分析表明,初始 PSA(P=0.00)、活检标本中的神经周围侵犯(P=0.00)、Gleason 评分(P=0.04)、EBRT 剂量(P=0.02)和阳性切缘(P=0.00)是复发的独立预测因素。这些变量构建了决策树模型。在 EBRT 队列中,PSA 最低点<0.3ng/ml 与最佳 5 年 bRFS 相关(PSA 最低点>1.3ng/ml 时为 96.6%和 56.5%)。RT 组和低剂量 EBRT(≤72Gy)的晚期生化失败(>5 年)更为常见。
低危和中危亚组中,PR 和 EBRT 的生化失败率相似。EBRT 队列的结局由经典的治疗前特征、神经周围侵犯、低剂量 EBRT(≤72Gy)和 PSA 最低点值决定。