医学
醋酸阿比特龙酯
前列腺癌
内科学
睾酮(贴片)
强的松
肿瘤科
阿比曲酮
雄激素
阉割
雄激素剥夺疗法
泌尿科
恩扎鲁胺
多西紫杉醇
化疗
癌症
雄激素受体
激素
作者
Cassandra Duarte,Antonio Jimeno,Elizabeth R. Kessler
出处
期刊:Drugs of Today
日期:2019-01-01
卷期号:55 (1): 5-5
被引量:2
标识
DOI:10.1358/dot.2019.55.1.2914339
摘要
Prostate cancer is one of the most common cancers in the United States, with an estimated incidence of 164,690 cases, accounting for 9.5% of all new cancer diagnoses. The mainstay of therapy for metastatic prostate cancer involves suppressing testosterone production through androgen deprivation therapy. However, nearly all patients on androgen deprivation therapy will develop resistance to hormone therapy. An improved understanding of the biology of castration resistance has allowed for the development of novel inhibitors of the androgen axis. Agents such as abiraterone acetate, which provides additional androgen suppression by inhibiting cytochrome P450 17A (CYP17A), have improved survival outcomes of patients with advanced prostate cancer. The longest experience with abiraterone acetate is in the metastatic castration-resistant setting. However, more recent trials have demonstrated that abiraterone acetate is an option for treatment earlier in the prostate cancer paradigm. This review will cover the current use of abiraterone acetate in combination with prednisone for the treatment of castration-resistant prostate cancer.
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