The Institute of Cancer Research, London, UK.
Guy's Hospital, London, UK; King's Hospital, London, UK; St Thomas' Hospital, London, UK.
Eur Urol. 2018 Jul;74(1):37-45. doi: 10.1016/j.eururo.2017.07.035. Epub 2017 Aug 23.
Enzalutamide and abiraterone acetate plus prednisone, which target the androgen receptor axis, have expanded the treatment of advanced prostate cancer. Retrospective analyses suggest some cross-resistance between these two drugs when used sequentially, but robust, prospective studies have not yet been reported.
To fulfil a regulatory postregistration commitment by evaluating the efficacy and safety of enzalutamide in patients with metastatic castration-resistant prostate cancer (mCRPC) who progressed following abiraterone acetate plus prednisone treatment.
DESIGN, SETTING, AND PARTICIPANTS: Multicentre, single-arm, open-label study, enrolled patients with progressing mCRPC after ≥24 wk of abiraterone acetate plus prednisone treatment. All patients maintained castration therapy during the trial. Prior chemotherapy was allowed but not required.
Patients received enzalutamide 160mg/d orally.
The primary endpoint was radiographic progression-free survival. Secondary endpoints were overall survival, prostate-specific antigen (PSA) response, and time-to-PSA progression. Safety data were also assessed. Kaplan-Meier methods were used to descriptively analyse time-to-event endpoints.
Overall, 214 patients received enzalutamide treatment, 145 of whom were chemotherapy-naïve. Median radiographic progression-free survival was 8.1 mo (95% confidence interval: 6.1-8.3); median overall survival had not been reached. Unconfirmed PSA response rate was 27% (48 of 181). Median time-to-PSA progression was 5.7 mo (95% confidence interval: 5.6-5.8). The most common treatment-emergent adverse events were fatigue (32%), decreased appetite (25%), asthenia (18%), back pain (17%), and arthralgia (16%). No seizures were reported.
Enzalutamide showed antitumour activity in some patients with mCRPC who had previously progressed following ≥24 wk of abiraterone acetate plus prednisone treatment.
Patients with mCRPC who progressed on previous abiraterone acetate plus prednisone treatment, with or without prior chemotherapy, received enzalutamide. Although cross-resistance between the two agents was observed in a majority of patients, some still benefited from enzalutamide treatment.
恩杂鲁胺和醋酸阿比特龙联合泼尼松可靶向作用于雄激素受体轴,已扩展了晚期前列腺癌的治疗选择。回顾性分析提示这两种药物序贯应用时存在一定的交叉耐药性,但尚未有强有力的前瞻性研究报道。
通过评估恩杂鲁胺在醋酸阿比特龙联合泼尼松治疗后进展的转移性去势抵抗性前列腺癌(mCRPC)患者中的疗效和安全性,满足监管注册后承诺。
设计、地点和参与者:这是一项多中心、单臂、开放标签研究,招募了醋酸阿比特龙联合泼尼松治疗≥24 周后进展的 mCRPC 患者。所有患者在试验期间维持去势治疗。允许但不要求有化疗史。
患者接受恩杂鲁胺 160mg/d 口服治疗。
主要终点为影像学无进展生存期。次要终点包括总生存期、前列腺特异抗原(PSA)应答和 PSA 进展时间。还评估了安全性数据。Kaplan-Meier 法用于描述性分析时间事件终点。
总体而言,214 例患者接受了恩杂鲁胺治疗,其中 145 例患者无化疗史。中位影像学无进展生存期为 8.1 个月(95%置信区间:6.1-8.3);中位总生存期尚未达到。未确认的 PSA 缓解率为 27%(48/181)。PSA 进展时间的中位数为 5.7 个月(95%置信区间:5.6-5.8)。最常见的治疗相关不良事件为疲乏(32%)、食欲下降(25%)、乏力(18%)、背痛(17%)和关节痛(16%)。无癫痫发作报告。
恩杂鲁胺在既往接受醋酸阿比特龙联合泼尼松治疗≥24 周后进展的部分 mCRPC 患者中具有抗肿瘤活性。
既往接受醋酸阿比特龙联合泼尼松治疗后进展的 mCRPC 患者,无论是否接受过化疗,均接受了恩杂鲁胺治疗。尽管在大多数患者中观察到两种药物之间存在交叉耐药,但一些患者仍从恩杂鲁胺治疗中获益。