Institut de Recherche Clinique, Université Catholique de Louvain, Brussels, Belgium.
Aarhus University Hospital, Aarhus, Denmark.
Lancet Oncol. 2014 May;15(6):592-600. doi: 10.1016/S1470-2045(14)70129-9. Epub 2014 Apr 14.
The androgen receptor inhibitor enzalutamide is approved for the treatment of metastatic castration-resistant prostate cancer that has progressed on docetaxel. Our aim was to assess the activity and safety of enzalutamide monotherapy in men with hormone-naive prostate cancer.
This trial is an ongoing open-label, single-arm, phase 2 study, done across 12 European sites. Men aged over 18 years, with hormone-naive prostate cancer for whom hormone therapy was indicated, and who had non-castration levels of testosterone and prostate-specific antigen (PSA) of 2 ng/mL or greater at screening, and an Eastern Cooperative Oncology Group score of 0, received oral enzalutamide 160 mg/day. The primary outcome was the proportion of patients with an 80% or greater decline in PSA at week 25. All analyses included all patients who had received at least one dose of the study drug. This study is registered with ClinicalTrials.gov, number NCT01302041.
67 men were enrolled into the study. 62 patients (92.5%, 95% CI 86.2-98.8) had a decline in PSA of 80% or greater at week 25. The most commonly reported treatment-emergent adverse events up to week 25 were gynaecomastia (n=24), fatigue (n=23), nipple pain (n=13), and hot flush (n=12), all of which were of mild to moderate severity. Nine patients had a treatment-emergent adverse event of grade 3 or higher, most of which were reported in one patient each, except for pneumonia (grade 3, two patients) and hypertension (grade 3, four patients). Five patients reported serious adverse events, none of which were deemed to be treatment related.
Our findings suggest that enzalutamide monotherapy in men with hormone-naive prostate cancer of varying severity provides a level of disease suppression, and was generally well tolerated. These findings provide a rationale for further investigation of clinical response and outcomes with enzalutamide in non-castrate men with prostate cancer.
雄激素受体抑制剂恩扎鲁胺获批用于治疗多西他赛治疗后进展的转移性去势抵抗性前列腺癌。我们的目的是评估恩扎鲁胺单药治疗激素初治前列腺癌患者的疗效和安全性。
这是一项正在进行的、开放标签、单臂、2 期临床试验,在欧洲 12 个地点进行。年龄在 18 岁以上、患有需要激素治疗的激素初治前列腺癌、且在筛选时非去势状态下的睾酮和前列腺特异性抗原(PSA)水平为 2ng/ml 或以上、东部肿瘤协作组(ECOG)评分为 0 的患者,接受口服恩扎鲁胺 160mg/天。主要终点是在第 25 周时 PSA 下降 80%或更多的患者比例。所有分析均包括至少接受一剂研究药物的所有患者。该研究在 ClinicalTrials.gov 注册,编号为 NCT01302041。
共有 67 名男性入组该研究。62 名患者(92.5%,95%CI 86.2-98.8)在第 25 周时 PSA 下降 80%或更多。至第 25 周时最常报告的治疗中出现的不良事件为男性乳房发育(n=24)、疲劳(n=23)、乳头疼痛(n=13)和热潮红(n=12),均为轻至中度。9 名患者出现 3 级或以上的治疗中出现的不良事件,其中多数为 1 例患者各出现 1 次,除肺炎(3 级,2 例)和高血压(3 级,4 例)各出现 2 例外。5 名患者报告了严重不良事件,均与治疗无关。
我们的研究结果表明,恩扎鲁胺单药治疗不同严重程度的激素初治前列腺癌患者可提供一定程度的疾病抑制,且总体耐受性良好。这些发现为进一步研究恩扎鲁胺在非去势男性前列腺癌患者中的临床反应和结局提供了依据。