Merseburger Axel S, Haas Gabriel P, von Klot Christoph-A
Department of Urology and Urologic Oncology, Hannover Medical School (MHH), Carl Neuberg Str. 1, 30625 Hannover, Germany.
Astellas Global Medical Affairs, Inc., Northbrook, IL, USA.
Ther Adv Urol. 2015 Feb;7(1):9-21. doi: 10.1177/1756287214555336.
Enzalutamide is an oral androgen receptor inhibitor that targets multiple steps in the androgen receptor signaling pathway. In the randomized phase III AFFIRM study, significant improvements in survival versus placebo were observed when enzalutamide was used as a treatment for patients with metastatic castration-resistant prostate cancer (mCRPC) following prior treatment with docetaxel. Additional benefits included significant delay in time to first skeletal-related event, and improvement in several measures of pain and health-related quality of life. Treatment effects were consistent across all prespecified subgroups. The phase III PREVAIL study evaluated enzalutamide versus placebo in patients with mCRPC who had not received chemotherapy. Enzalutamide significantly decreased the risk of radiographic progression and death. There were also significant improvements in all secondary and prespecified exploratory endpoints, including delayed initiation of chemotherapy, reduction in risk of first skeletal-related event and a high percentage of patients with objective response compared with placebo. Enzalutamide was also studied in hormone naïve patients (as monotherapy) in a small, open-label phase II study in patients with prostate cancer who were eligible for androgen-deprivation therapy. A prostate-specific antigen (PSA) response, defined as ⩾80% decline in PSA level from baseline at week 25, was achieved in 92.5% of patients. Long-term follow up is ongoing. Despite differences between these three trials, enzalutamide displayed a favorable safety profile in all three patient populations. Similar rates of adverse events between the enzalutamide and placebo groups were observed in AFFIRM and PREVAIL, with fatigue, diarrhea, back pain and hot flashes being more common with enzalutamide than with placebo. Hypertension was reported at a higher rate in the enzalutamide group than in the placebo group in PREVAIL. Breast-related disorders associated with enzalutamide treatment were also reported in the Monotherapy trial. Few seizures were reported in any trial. Enzalutamide is being studied in several early disease state populations.
恩杂鲁胺是一种口服雄激素受体抑制剂,作用于雄激素受体信号通路的多个环节。在随机III期AFFIRM研究中,恩杂鲁胺用于多西他赛治疗后的转移性去势抵抗性前列腺癌(mCRPC)患者时,与安慰剂相比生存期显著改善。其他益处包括首次骨相关事件发生时间显著延迟,以及疼痛和健康相关生活质量的多项指标有所改善。在所有预先设定的亚组中治疗效果一致。III期PREVAIL研究评估了恩杂鲁胺与安慰剂用于未接受化疗的mCRPC患者。恩杂鲁胺显著降低影像学进展和死亡风险。所有次要和预先设定的探索性终点也有显著改善,包括化疗起始延迟、首次骨相关事件风险降低,与安慰剂相比客观缓解的患者比例较高。在一项小型开放标签II期研究中,还对未接受过激素治疗的前列腺癌患者(作为单一疗法)使用恩杂鲁胺进行了研究,这些患者符合雄激素剥夺治疗条件。92.5%的患者实现了前列腺特异性抗原(PSA)反应,定义为第25周时PSA水平较基线下降⩾80%。长期随访正在进行。尽管这三项试验存在差异,但恩杂鲁胺在所有三类患者人群中均显示出良好的安全性。在AFFIRM和PREVAIL研究中,恩杂鲁胺组和安慰剂组的不良事件发生率相似,与安慰剂相比,恩杂鲁胺组疲劳、腹泻、背痛和潮热更为常见。在PREVAIL研究中,恩杂鲁胺组高血压报告率高于安慰剂组。单一疗法试验中也报告了与恩杂鲁胺治疗相关的乳腺疾病。在任何试验中癫痫发作报告较少。目前正在对恩杂鲁胺在几种早期疾病状态人群中进行研究。