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CUOG randomized trial of neoadjuvant androgen ablation before radical prostatectomy: 36-month post-treatment PSA results. Canadian Urologic Oncology Group.

机译:前列腺癌根治术前新辅助雄激素消融的CUOG随机试验:治疗后PSA结果36个月。加拿大泌尿外科肿瘤学小组。

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OBJECTIVES: To test the hypothesis that neoadjuvant androgen ablation before radical prostatectomy reduces the likelihood of biochemical progression at 36 months. METHODS: Two hundred thirteen patients with localized prostate cancer were randomized to radical prostatectomy alone (Sx, n = 101) or a 12-week course of 300 mg of cyproterone acetate daily followed by surgery (CPA, n = 112). Biochemical progression (two consecutive detectable prostate-specific antigen [PSA] values) was determined for the entire group and by baseline PSA, Gleason score, clinical stage, and pathologic stage. RESULTS: The probability of biochemical progression at 36 months was similar in both groups (CPA 40.2%, Sx 30.1%; P = 0.3233). CPA patients with baseline serum PSA between 25 and 50 ng/mL had a lower probability of biochemical progression (CPA 63.5%, Sx 84.6%; P = 0.0038). No difference in the probability of biochemical progression was seen between groups when analyzed by clinical stage or Gleason score. When analyzed by pathologic margin status, no difference was observed in the probability of biochemical progression in patients with organ-confined disease (P = 0.4484). There was a trend for a higher probability of progression in the neoadjuvant arm in patients with positive and negative surgical margins (P = 0.0105, P = 0.0459; alpha = 0.005 with Bonferroni adjustment). CONCLUSIONS: Neoadjuvant androgen ablation with CPA reduces the positive margin rate significantly but does not result in a difference in biochemical progression at 3 years. This may be due to a lack of sufficient follow-up, insufficient power of the trial to demonstrate a small benefit, or a true lack of benefit of neoadjuvant androgen ablation before radical prostatectomy.
机译:目的:为了检验假说,在前列腺癌根治术前新辅助雄激素消融可减少36个月生化进展的可能性。方法:213例局限性前列腺癌患者被随机分为单纯根治性前列腺切除术(Sx,n = 101)或每天接受300 mg醋酸环丙孕酮的12周疗程,然后进行手术(CPA,n = 112)。通过基线PSA,Gleason评分,临床分期和病理分期确定整个组的生化进程(两个连续可检测的前列腺特异性抗原[PSA]值)。结果:两组在36个月时生化进展的可能性相似(CPA 40.2%,Sx 30.1%; P = 0.3233)。基线血清PSA在25至50 ng / mL之间的CPA患者生化进展的可能性较低(CPA 63.5%,Sx 84.6%; P = 0.0038)。通过临床分期或格里森评分分析时,各组之间生化进展的可能性没有差异。通过病理学边缘状态分析时,在器官受限疾病患者中,生化进展的可能性未观察到差异(P = 0.4484)。在手术切缘阳性和阴性的患者中,新辅助臂中发生进展的可能性更高(P = 0.0105,P = 0.0459;经Bonferroni调整的α= 0.005)。结论:新辅助雄激素联合CPA消融可显着降低阳性切缘率,但在3年内不会导致生化进展差异。这可能是由于缺乏足够的随访,试验的能力不足以证明获益少,或者是由于前列腺癌根治术前新辅助雄激素消融的真正缺乏。

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