Radiation Oncology, McGill University Health Centre, Montreal, Quebec, Canada.
Cancer. 2013 Jun 1;119(11):1999-2004. doi: 10.1002/cncr.28019. Epub 2013 Mar 15.
The objective of this study was to assess the impact of a prostate-specific antigen (PSA) complete response (PSA-CR), measured at the end of external-beam radiotherapy and short-term hormone therapy, on treatment outcomes.
The phase 3 Radiation Therapy Oncology Group 9413 trial, as part of its original protocol, used the assessment of PSA-CR (ie, PSA ≤0.3 ng/mL) at the end of short-term HT as a secondary endpoint. Short-term HT consisted of futamide plus a lutenizing hormone-releasing hormone agonist for 4 months. The Kaplan-Meier method was used to estimate overall survival (OS) and disease-free survival. Cumulative incidence was used to estimate biochemical failure, distant metastasis, and disease-specific survival. Univariate and multivariate analyses were performed to correlate PSA-CR after short-term hormone therapy with all endpoints, and the following variables were considered for analysis: PSA at baseline, Gleason score, treatment arm, age, and baseline testosterone status. Phoenix consensus definition was used to define PSA failure.
For 1070 evaluable patients, the median PSA at the end of short-term hormone therapy was 0.2 ng/mL. In total, 744 patients (70%) had a PSA-CR. At a median follow-up of 7.2 years, failure to obtain a PSA-CR was associated significantly with worse disease-specific survival (P = .0003; hazard ratio [HR], 2.03; 95% confidence interval [CI], 1.38-2.97), with worse disease-free survival (P = .003; HR, 1.28; 95% CI, 1.09-1.50), and with a higher incidence of distant metastasis (P = .0002; HR, 1.92; 95% CI, 1.37-2.69) and biochemical failure (P < .0001; HR, 1.57; 95% CI, 1.29-1.91). Other factors that were associated with worse disease-specific survival were Gleason scores from 8 to 10 (P = .0002; HR, 3.06; 95% CI, 1.71-5.47) and PSA levels >20 ng/mL (P = .04; HR, 1.55; 95% CI, 1.02-2.30).
The current results indicated that failure to obtain a PSA-CR (PSA ≤0.3 ng/mL) after short-term hormone therapy and external-beam radiotherapy appears to be an independent predictor of unfavorable outcomes and could help identify patients who may benefit from the addition of long-term androgen ablation.
本研究旨在评估前列腺特异性抗原(PSA)完全缓解(PSA-CR)在结束外照射放疗和短期激素治疗后对治疗结果的影响。
作为其原始方案的一部分,放射治疗肿瘤学组 9413 期试验使用 PSA-CR(即 PSA≤0.3ng/mL)在短期 HT 结束时作为次要终点进行评估。短期 HT 包括氟他胺加促黄体激素释放激素激动剂治疗 4 个月。采用 Kaplan-Meier 法估计总生存(OS)和无病生存。累积发生率用于估计生化失败、远处转移和疾病特异性生存。采用单变量和多变量分析将短期激素治疗后 PSA-CR 与所有终点相关联,并对以下变量进行分析:基线 PSA、Gleason 评分、治疗臂、年龄和基线睾酮状态。Phoenix 共识定义用于定义 PSA 失败。
对于 1070 例可评估患者,短期激素治疗结束时的中位 PSA 为 0.2ng/mL。共有 744 例(70%)患者 PSA-CR。中位随访 7.2 年后,未能获得 PSA-CR 与较差的疾病特异性生存显著相关(P=0.0003;风险比[HR],2.03;95%置信区间[CI],1.38-2.97),与较差的无病生存(P=0.003;HR,1.28;95% CI,1.09-1.50)和更高的远处转移发生率(P=0.0002;HR,1.92;95% CI,1.37-2.69)和生化失败(P<.0001;HR,1.57;95% CI,1.29-1.91)相关。与较差的疾病特异性生存相关的其他因素包括 Gleason 评分 8-10(P=0.0002;HR,3.06;95% CI,1.71-5.47)和 PSA 水平>20ng/mL(P=0.04;HR,1.55;95% CI,1.02-2.30)。
目前的结果表明,短期激素治疗和外照射放疗后未能获得 PSA-CR(PSA≤0.3ng/mL)似乎是不良结局的独立预测因素,并可能有助于识别可能受益于长期雄激素剥夺的患者。