预测永久性前列腺近距离治疗患者PSA无复发生存的风险概况。

L Potters, C Cha, G Oshinsky, E Venkatraman, M Zelefsky, S Leibel
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引用次数: 0

摘要

目的:综合风险概况有助于评估前列腺特异性抗原无复发生存(PSA-RFS)的可能性局限性前列腺癌患者。本回顾性分析报告了一大批接受超声引导下经会阴间质永久性前列腺近距离放射治疗(TIPPB)的患者的预后因素和风险概况。患者和方法:在1992年6月至1997年11月期间,717例临床局限性前列腺癌患者连续接受了TIPPB治疗。钯-103 (103Pd) (n = 539)或碘-125 (125I) (n = 178)源的使用剂量分别为120 Gy和144 Gy。111例患者接受了外束照射(41.4或45 Gy)和TIPPB (103Pd, 90 Gy和125I, 108 Gy)联合治疗。112例患者在TIPPB前接受了雄激素消融治疗。根据PSA <或= 10和Gleason评分<或= 6的预处理因素将患者分组为风险概况。符合这两个标准的患者被归为有利组(n = 334)。不符合其中一项标准者被归类为中度风险(n = 261),不符合两项标准者被归类为不良风险(n = 261)。PSA- rfs是根据美国治疗放射学和肿瘤学会共识会议对PSA失败的定义计算的。中位随访为41个月(范围14-82个月)。结果:5年精算PSA-RFS生存率为82%。多因素Cox回归分析发现PSA和Gleason评分是预测生化结局的高度显著因素。使用PSA最低定义<或= 1.0 ng/mL和<或= 0.5 ng/mL的危险风险比都是预后的重要预测因子,0.5 ng/mL最低水平仅略好(最低水平<或= 1.0的风险比= 2.78;最低点风险比<或= 0.5 = 3.57)。有利风险患者的5年精算PSA-RFS为93%,而中等风险和不利风险组的5年PSA-RFS分别为77%和62%。493例患者接受近距离治疗,无外束照射或雄激素消融。在该组中,有利风险、中等风险和不利风险患者的5年psa - rfs分别为92%、74%和55%。讨论:这项检查TIPPB的回顾性研究显示了出色的5年精算PSA-RFS率。基于预后因素的多变量分析结果的风险概况分配确定了接受TIPPB患者的预期PSA-RFS。
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Risk profiles to predict PSA relapse-free survival for patients undergoing permanent prostate brachytherapy.

Purpose: Combined risk profiles are helpful in assessing the likelihood of prostate-specific antigen relapse-free survival (PSA-RFS) for patients with localized prostate cancer. This retrospective analysis reports the 5-year biochemical outcome of a large cohort of patients according to prognostic factors and risk profiles for patients undergoing ultrasound-guided transperineal interstitial permanent prostate brachytherapy (TIPPB).

Patients and methods: Seven hundred seventeen consecutive patients with clinically localized prostate cancer treated between June 1992 and November 1997 underwent TIPPB. Palladium-103 (103Pd) (n = 539) or iodine-125 (125I) (n = 178) sources were utilized to a prescribed dose of 120 Gy and 144 Gy, respectively. One hundred eleven patients received combined external-beam irradiation (41.4 or 45 Gy) and TIPPB (103Pd, 90 Gy, and 125I, 108 Gy). One hundred twelve patients received androgen ablation therapy in advance of TIPPB. Patients were grouped into risk profiles based on pretreatment factors that consisted of PSA < or = 10 and Gleason score < or = 6. Patients meeting both criteria were classified as favorable (n = 334). Those not fulfilling one criteria were classified as intermediate risk (n = 261), and those not fulfilling two criteria were classified as unfavorable risk (n = 261). PSA-RFS was calculated based on the American Society of Therapeutic Radiology and Oncology consensus conference definition of PSA failure. The median follow-up was 41 months (range, 14-82 months).

Results: The actuarial PSA-RFS survival at 5 years was 82%. Multivariate Cox regression analysis identified PSA and Gleason score as highly significant factors predicting for biochemical outcome. Hazard risk ratios using a nadir definition of the PSA as < or = 1.0 ng/mL and < or = 0.5 ng/mL were each significant predictors of outcome with the 0.5 ng/mL nadir level only slightly better (risk ratio for nadir < or = 1.0 = 2.78; risk ratio for nadir < or = 0.5 = 3.57). Favorable-risk patients had a 5-year actuarial PSA-RFS of 93%, whereas intermediate-risk and unfavorable-risk groups had 5-year PSA-RFSs of 77% and 62%, respectively. Four hundred ninety-three patients underwent brachytherapy without external-beam irradiation or androgen ablation. From this group, the 5-year PSA-RFSs for the favorable-risk, intermediate-risk, and unfavorable-risk patients were 92%, 74%, and 55%, respectively.

Discussion: This retrospective study examining TIPPB demonstrated excellent 5-year actuarial PSA-RFS rates. The assignment of risk profiles based on the results of multivariate analysis of prognostic factors identifies the expected PSA-RFS for patients undergoing TIPPB.

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