Division of Medical Oncology, Department of Internal Medicine, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
GU Medical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.
Curr Treat Options Oncol. 2019 Feb 11;20(2):14. doi: 10.1007/s11864-019-0611-z.
Nonmetastatic castration-resistant prostate cancer (nmCRPC) comprises a relatively narrow niche of advanced prostate cancer, but the treatment landscape for men with nmCRPC has drastically changed over the past year. Prior to the SPARTAN and PROSPER trials, men with nmCRPC were commonly treated with first-generation androgen receptor antagonists, such as bicalutamide or flutamide, or with estrogens or ketoconazole, none of which were associated with any proven survival benefit. The SPARTAN trial evaluated apalutamide versus placebo for men with nmCRPC and found that apalutamide significantly improved metastasis-free survival (MFS), the primary endpoint of this trial. Similarly, the PROSPER trial showed that enzalutamide significantly improved MFS compared with placebo for men with nmCRPC. In both trials, the data for overall survival was immature at the time of analysis. The SPARTAN and PROSPER trials led to the approval of apalutamide and enzalutamide, respectively, for men with nmCRPC. More recently, the phase 3 trial ARAMIS showed that darolutamide, a novel androgen receptor antagonist, also improves MFS compared with placebo for men with nmCRPC, and this trial is expected to garner regulatory approval for darolutamide in the nmCRPC setting. Novel imaging modalities are becoming more prevalent for the diagnostic evaluation of men with prostate cancer and are more sensitive than conventional bone or CT scans for detection of oligometastatic disease that previously was undetected. These modalities are likely to reduce the incidence and prevalence of nmCRPC in the near future. Ultimately, the treatment options for men with nmCRPC have significantly improved over the past 2 years.
非转移性去势抵抗性前列腺癌(nmCRPC)构成了晚期前列腺癌的一个相对狭窄的亚群,但在过去的一年中,nmCRPC 患者的治疗格局发生了巨大变化。在 SPARTAN 和 PROSPER 试验之前,nmCRPC 患者通常接受第一代雄激素受体拮抗剂治疗,如比卡鲁胺或氟他胺,或接受雌激素或酮康唑治疗,但这些治疗均与任何已证实的生存获益无关。SPARTAN 试验评估了阿帕鲁胺与安慰剂治疗 nmCRPC 男性患者的效果,发现阿帕鲁胺可显著改善无转移生存期(MFS),这是该试验的主要终点。同样,PROSPER 试验表明,与安慰剂相比,恩扎卢胺可显著改善 nmCRPC 男性患者的 MFS。在这两项试验中,分析时总体生存数据尚未成熟。SPARTAN 和 PROSPER 试验分别导致阿帕鲁胺和恩扎卢胺获得批准,用于治疗 nmCRPC 男性患者。最近,III 期 ARAMIS 试验表明,新型雄激素受体拮抗剂达罗他胺也可改善 nmCRPC 男性患者的 MFS,预计该试验将为达罗他胺在 nmCRPC 环境下获得监管批准。新型影像学检查方法越来越普遍地用于前列腺癌男性患者的诊断评估,与传统的骨扫描或 CT 扫描相比,这些方法对寡转移疾病的检测更敏感,而之前这些寡转移疾病是无法检测到的。这些方法可能会在不久的将来降低 nmCRPC 的发病率和患病率。最终,在过去的 2 年中,nmCRPC 男性患者的治疗选择得到了显著改善。