Department of Urology, Erasmus University Medical Center, Rotterdam, the Netherlands.
BJU Int. 2010 Jul;106(2):182-7. doi: 10.1111/j.1464-410X.2009.08981.x. Epub 2009 Nov 13.
Study Type - Therapy (RCT) Level of Evidence 1b OBJECTIVE To compare the activity of degarelix, a new gonadotrophin-releasing hormone (GnRH) blocker, with leuprolide depot 7.5 mg in the control of total serum alkaline phosphatase (S-ALP) levels in patients with prostate cancer. PATIENTS AND METHODS In the randomized, phase III trial (CS21), patients with histologically confirmed prostate cancer (all stages), were randomized to one of three regimens: degarelix subcutaneous 240 mg for 1 month followed by monthly maintenance doses of 80 mg or 160 mg, or intramuscular leuprolide 7.5 mg/month. Patients receiving leuprolide could also receive antiandrogens for flare protection. We report exploratory S-ALP analyses from CS21, focusing on the comparison of degarelix 240/80 mg with leuprolide 7.5 mg, in line with the recent approvals of this dose by the USA Food and Drug Administration and the European Medicines Agency. RESULTS Overall, 610 patients were included, with a median age of 73 years and median prostate-specific antigen (PSA) level of 19.0 ng/mL. Baseline S-ALP levels were high in metastatic patients and highest in patients with metastatic disease and a haemoglobin level of <13 g/dL. In metastatic disease, after initial peaks in both groups, S-ALP levels were suppressed below baseline with degarelix but were maintained around baseline with leuprolide. The late rise in S-ALP seen with leuprolide was not apparent with degarelix. The pattern of S-ALP response was similar in patients with a baseline PSA level of > or =50 ng/mL. Between-treatment differences in patients with metastatic disease and those with a PSA level of > or =50 ng/mL were significant at day 364 (P = 0.014 and 0.007, respectively). CONCLUSION Patients with metastatic disease or those with PSA levels of > or =50 ng/mL at baseline had greater reductions in S-ALP levels with degarelix than with leuprolide. Patients in the degarelix group maintained S-ALP suppression throughout the study, in contrast to those in the leuprolide group. This suggests that degarelix might offer better S-ALP control than leuprolide and might prolong control of skeletal metastases, compared with GnRH agonists, over a 1-year treatment period.
研究类型 - 治疗(RCT)证据水平 1b 目的:比较新型促性腺激素释放激素(GnRH)拮抗剂 degarelix 与亮丙瑞林 depot 7.5mg 在控制前列腺癌患者总血清碱性磷酸酶(S-ALP)水平方面的活性。 患者和方法:在随机、III 期试验(CS21)中,组织学证实患有前列腺癌(所有阶段)的患者被随机分配至以下三种方案之一:皮下注射 degarelix 240mg 1 个月,随后每月维持剂量 80mg 或 160mg,或每月肌内注射亮丙瑞林 7.5mg。接受亮丙瑞林的患者也可以接受抗雄激素治疗以预防 flare。我们报告了 CS21 的探索性 S-ALP 分析结果,重点比较了 degarelix 240/80mg 与亮丙瑞林 7.5mg 的疗效,这与美国食品和药物管理局和欧洲药品管理局最近批准的该剂量一致。 结果:总体而言,610 名患者被纳入研究,中位年龄为 73 岁,中位前列腺特异性抗原(PSA)水平为 19.0ng/ml。转移性疾病患者的基线 S-ALP 水平较高,血红蛋白水平<13g/dL 的转移性疾病患者的 S-ALP 水平最高。在转移性疾病中,两组患者在初始峰值后,degarelix 可将 S-ALP 水平抑制至基线以下,但亮丙瑞林可将 S-ALP 水平维持在基线附近。亮丙瑞林出现的晚期 S-ALP 升高在 degarelix 中并不明显。在基线 PSA 水平≥50ng/ml 的患者中,S-ALP 反应模式相似。在转移性疾病患者和基线 PSA 水平≥50ng/ml 的患者中,治疗间差异在第 364 天时具有统计学意义(分别为 P=0.014 和 0.007)。 结论:与亮丙瑞林相比,基线时患有转移性疾病或 PSA 水平≥50ng/ml 的患者使用 degarelix 可使 S-ALP 水平降低更大。与亮丙瑞林组相比,degarelix 组患者在整个研究期间维持 S-ALP 抑制。这表明与 GnRH 激动剂相比,degarelix 可能在 1 年治疗期间提供更好的 S-ALP 控制,并可能延长对骨骼转移的控制。