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Darolutamide: a novel androgen-signaling agent in nonmetastatic castration-resistant prostate cancer

机译:达洛鲁胺:一种用于非转移性去势抵抗性前列腺癌的新型雄激素信号剂

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摘要

ARAMIS is an international Phase III trial demonstrating the beneficial role of darolutamide, a novel anti-androgen that has been found to prolong metastasis-free survival in men with nonmetastatic castration-resistant prostate cancer. Darolutamide is a novel nonsteroidal androgen receptor antagonist that has unique structurally distinct properties with low blood–brain barrier penetration that was shown to improve metastasis-free survival by 22 months compared to placebo (40.4 months 18.4 months), reducing the risk of metastasis or death by 59%. Darolutamide also showed improvement in secondary and exploratory endpoints including progression-free survival, prolonged time to PSA progression, PSA response and time to initiating additional antineoplastic therapy, time to pain progression, and time to cytotoxic chemotherapy, but overall survival is not yet reached in either the darolutamide or the placebo arm. Adverse events leading to trial discontinuation were similar at 8.9% and 8.7% in the darolutamide and placebo arms, respectively. Darolutamide was filed as a new drug application to the United States Food and Drug Administration (US FDA) for use in the setting of nonmetastatic castration-resistant prostate cancer.
机译:ARAMIS是一项国际性的III期临床试验,证明了darolutamide(一种新型的抗雄激素药物)的有益作用,该药物已被发现可延长非转移性去势抵抗性前列腺癌男性的无转移生存期。达洛鲁胺是一种新型的非甾体雄激素受体拮抗剂,具有独特的结构独特的特性和低的血脑屏障渗透性,与安慰剂(40.4个月和18.4个月)相比,可将无转移生存期提高22个月,从而降低了转移或死亡的风险减少了59%。达洛鲁胺还显示出继发性和探索性终点的改善,包括无进展生存期,PSA进展时间延长,PSA反应和开始其他抗肿瘤治疗的时间,疼痛进展时间以及细胞毒性化学疗法的时间,但尚无总生存期。达洛鲁胺或安慰剂组。导致停用试验的不良事件在达洛鲁胺和安慰剂组中分别为8.9%和8.7%。达洛鲁胺已作为新药申请提交美国食品和药物管理局(US FDA),用于治疗非转移性去势抵抗性前列腺癌。

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