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Abiraterone acetate: A review of its use in patients with metastatic castration-resistant prostate cancer

机译:醋酸阿比特龙:其在转移性去势抵抗性前列腺癌患者中的应用综述

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摘要

Abiraterone acetate (Zytiga?) is an orally administered, selective inhibitor of the 17α-hydroxylase and C17,20-lyase enzymatic activities of cytochrome P450 (CYP) 17. CYP17 is required for androgen biosynthesis, with androgen receptor signalling crucial in the progression from primary to metastatic prostate cancer. Abiraterone acetate is approved in the European Union and the US, in combination with prednisone or prednisolone, for the treatment of men with metastatic castration-resistant prostate cancer (CRPC).When administered in combination with prednisone in a placebocontrolled, multinational phase III study, abiraterone acetate significantly prolonged overall survival and radiographic progression-free survival (rPFS) in men with metastatic CRPC who had previously received docetaxel. In men with metastatic CRPC who had not previously received chemotherapy participating in a placebo-controlled, multinational phase III study, there was a strong trend towards an overall survival benefit, a significant prolongation in rPFS and significant delays in clinical decline, the need for chemotherapy and the onset of pain observed. Given the nature of the therapy, the overall tolerability profile of abiraterone acetate, in combination with prednisone, was acceptable in men with metastatic CRPC. Abiraterone acetate is associated with hypokalaemia, hypertension, and fluid retention or oedema, secondary to its mechanism of action, and with cardiac adverse events and hepatotoxicity; however, in the phase III studies the incidences of the most frequently reported grade 3 or 4 adverse events of special interest were relatively low. Although the final overall survival data in menwithmetastatic CRPC who have not previously received chemotherapy are awaited, current evidence indicates that abiraterone acetate is a useful option for the treatment of metastatic CRPC.
机译:乙酸阿比特龙酯(Zytiga?)是口服施用的细胞色素P450(CYP)17的17α-羟化酶和C17,20-裂合酶酶活性的选择性抑制剂。CYP17是雄激素生物合成所必需的,雄激素受体信号在从原发于转移性前列腺癌。醋酸阿比特龙酯在欧洲联盟和美国已获批准与泼尼松或泼尼松龙联用,用于治疗转移性去势抵抗性前列腺癌(CRPC)的男性。在安慰剂对照的多国III期研究中,与泼尼松联用时,醋酸阿比特龙显着延长了先前曾接受多西他赛治疗的转移性CRPC男性的总生存期和无影像学无进展生存期(rPFS)。在先前未接受过化疗的转移性CRPC男性中,参加安慰剂对照的多国III期研究的趋势是,其总体生存获益,rPFS显着延长,临床下降显着延迟,需要化疗的趋势很明显。并观察到疼痛的发作。根据治疗的性质,乙酸阿比特龙酯与泼尼松联用的总体耐受性在转移性CRPC男性中是可以接受的。乙酸阿比特龙酯是继发于其作用机理的低血钾症,高血压和体液retention留或水肿,并伴有心脏不良事件和肝毒性。但是,在III期研究中,最常报告的特别感兴趣的3级或4级不良事件的发生率相对较低。尽管等待尚未接受过化疗的转移性CRPC的最终总体生存数据,但目前的证据表明乙酸乙酸阿比特龙酯是治疗转移性CRPC的有用选择。

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