多西紫杉醇
恩扎鲁胺
前列腺癌
医学
雄激素受体
肿瘤科
醋酸阿比特龙酯
雄激素剥夺疗法
内科学
背景(考古学)
临床试验
雄激素
卡巴齐塔塞尔
药理学
癌症
激素
生物
古生物学
作者
Jacob J. Adashek,Jarred P Reed,Ankita Tandon,Stephen J. Freedland,Edwin M. Posadas,Neil A. Bhowmick,Leland W.K. Chung,Michael R. Freeman,Robert A. Figlin,Jun Gong
标识
DOI:10.1016/j.clgc.2020.05.003
摘要
The addition of docetaxel and abiraterone to androgen deprivation therapy (ADT) heralded a new era in the first-line treatment of metastatic castration-sensitive prostate cancer (mCSPC). Following the success of these combination regimens, 3 new trials presented data on using enzalutamide or apalutamide in men with mCSPC, which showed similar success. These seminal trials collectively established the addition of docetaxel, enzalutamide, apalutamide, or abiraterone to ADT as standards in the upfront treatment of mCSPC. Notably, a subset of patients in these more recent trials were treated with a combination of docetaxel, ADT, and androgen receptor signaling inhibitors or maintenance androgen receptor signaling inhibitors after docetaxel and ADT that provided an initial glimpse into the efficacy of these triplet or maintenance strategies. We discuss the implications of these recent findings and place them in context of the current mCSPC treatment landscape.
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