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阿帕鲁胺治疗转移性去势抵抗性前列腺癌的概况:迄今的证据

Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date.

作者信息

Chong Julio T, Oh William K, Liaw Bobby C

机构信息

Department of Urology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Department of Medicine, Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Onco Targets Ther. 2018 Apr 12;11:2141-2147. doi: 10.2147/OTT.S147168. eCollection 2018.

Abstract

Advances in therapies have led to the approval of six therapeutic agents since 2004, each demonstrating overall survival benefit in randomized studies, and these have significantly improved the outlook for men facing metastatic castration-resistant prostate cancer (CRPC). More recently, efforts have been directed at trying to effect change at earlier phases of the disease. Apalutamide (ARN-509), a second-generation androgen receptor antagonist, recently received approval in the nonmetastatic (M0) CRPC space. Similar to enzalutamide, apalutamide inhibits the binding of androgen to androgen receptor (AR), nuclear translocation of the androgen-AR complex, and binding of AR transcription complex to DNA-binding sites and transcription elements. Phase I and II trial experience demonstrates the safety and tolerability of apalutamide, as well as its efficacy in effecting prostate-specific antigen response and radiographic-free survival in CRPC. US Food and Drug Administration approval in M0 CRPC was granted following positive results from the phase III SPARTAN study, where apalutamide demonstrated significant improvements in metastasis-free survival and time to symptomatic progression as compared to placebo.

摘要

自2004年以来,治疗方法的进步已促使六种治疗药物获批,每种药物在随机研究中均显示出总生存获益,这些药物显著改善了转移性去势抵抗性前列腺癌(CRPC)男性患者的前景。最近,人们致力于在疾病的更早期阶段实现改变。第二代雄激素受体拮抗剂阿帕鲁胺(ARN-509)最近在非转移性(M0)CRPC领域获得批准。与恩杂鲁胺相似,阿帕鲁胺可抑制雄激素与雄激素受体(AR)的结合、雄激素-AR复合物的核转位以及AR转录复合物与DNA结合位点和转录元件的结合。I期和II期试验经验证明了阿帕鲁胺的安全性和耐受性,以及其在CRPC中影响前列腺特异性抗原反应和无影像学进展生存期的疗效。在III期SPARTAN研究取得阳性结果后,美国食品药品监督管理局批准阿帕鲁胺用于M0 CRPC,在该研究中,与安慰剂相比,阿帕鲁胺在无转移生存期和至症状进展时间方面显示出显著改善。

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