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Target Oncol. 2020 Dec;15(6):791-799. doi: 10.1007/s11523-020-00779-x.
Oral darolutamide (Nubeqa™) is a novel second-generation, nonsteroidal, selective androgen receptor (AR) inhibitor indicated for the treatment of non-metastatic castration-resistant prostate cancer (nmCRPC). In the pivotal multinational, phase 3 ARAMIS trial in men with nmCRPC, relative to placebo plus ongoing androgen deprivation therapy (ADT), darolutamide (+ ADT) significantly prolonged metastasis-free survival (MFS) at the time of the primary analysis and overall survival (OS) at the time of the final OS analysis and was generally well tolerated in extended follow-up. Albeit long-term data from the real-world setting are required to fully define the safety profile of darolutamide, current evidence from the final ARAMIS analysis indicates that darolutamide has a low propensity for CNS-related adverse events (AEs) associated with other currently approved second-generation AR inhibitors. Given the efficacy and safety evidence from the final ARAMIS analysis and the key role of second-generation AR inhibitors in the management of nmCRPC, darolutamide + ADT represents an important emerging option for the treatment of men with nmCRPC who are at high risk of developing metastatic prostate cancer.
口服达罗鲁胺(Nubeqa™)是一种新型第二代非甾体类选择性雄激素受体(AR)抑制剂,用于治疗非转移性去势抵抗性前列腺癌(nmCRPC)。在 nmCRPC 男性的关键性多中心、III 期ARAMIS 试验中,与安慰剂加持续雄激素剥夺治疗(ADT)相比,达罗鲁胺(+ ADT)在主要分析时显著延长无转移生存(MFS),在最终总生存(OS)分析时显著延长 OS,并且在延长随访期间通常具有良好的耐受性。尽管需要来自真实世界环境的长期数据来全面定义达罗鲁胺的安全性概况,但最终 ARAMIS 分析的现有证据表明,与其他目前批准的第二代 AR 抑制剂相比,达罗鲁胺发生与中枢神经系统(CNS)相关不良事件(AE)的倾向较低。鉴于最终 ARAMIS 分析的疗效和安全性证据,以及第二代 AR 抑制剂在 nmCRPC 管理中的关键作用,达罗鲁胺+ADT 代表了一种重要的新兴治疗选择,适用于有发生转移性前列腺癌高风险的 nmCRPC 男性。