Testosterone suppression plus enzalutamide versus testosterone suppression plus standard antiandrogen therapy for metastatic hormone-sensitive prostate cancer (ENZAMET): an international, open-label, randomised, phase 3 trial

医学 多西紫杉醇 恩扎鲁胺 临床终点 前列腺癌 内科学 抗雄激素 氟他胺 人口 肿瘤科 中期分析 比卡鲁胺 睾酮(贴片) 随机对照试验 泌尿科 癌症 雄激素受体 环境卫生
作者
Christopher J. Sweeney,Andrew Martin,Martin R. Stockler,Stephen Begbie,Leanna Cheung,Kim N.,Simon Chowdhury,Mark Frydenberg,Lisa G. Horvath,Anthony M. Joshua,Nicola Jane Lawrence,Gavin Marx,John McCaffrey,Ray McDermott,Margaret McJannett,Scott North,Francis Parnis,Wendy R. Parulekar,David Pook,M. Neil Reaume
出处
期刊:Lancet Oncology [Elsevier BV]
卷期号:24 (4): 323-334 被引量:175
标识
DOI:10.1016/s1470-2045(23)00063-3
摘要

Background The interim analysis of the ENZAMET trial of testosterone suppression plus either enzalutamide or standard nonsteroidal antiandrogen therapy showed an early overall survival benefit with enzalutamide. Here, we report the planned primary overall survival analysis, with the aim of defining the benefit of enzalutamide treatment in different prognostic subgroups (synchronous and metachronous high-volume or low-volume disease) and in those who received concurrent docetaxel. Methods ENZAMET is an international, open-label, randomised, phase 3 trial conducted at 83 sites (including clinics, hospitals, and university centres) in Australia, Canada, Ireland, New Zealand, the UK, and the USA. Eligible participants were males aged 18 years or older with metastatic, hormone-sensitive prostate adenocarcinoma evident on CT or bone scanning with 99mTc and an Eastern Cooperative Oncology Group performance status score of 0–2. Participants were randomly assigned (1:1), using a centralised web-based system and stratified by volume of disease, planned use of concurrent docetaxel and bone antiresorptive therapy, comorbidities, and study site, to receive testosterone suppression plus oral enzalutamide (160 mg once per day) or a weaker standard oral non-steroidal antiandrogen (bicalutamide, nilutamide, or flutamide; control group) until clinical disease progression or prohibitive toxicity. Testosterone suppression was allowed up to 12 weeks before randomisation and for up to 24 months as adjuvant therapy. Concurrent docetaxel (75 mg/m2 intravenously) was allowed for up to six cycles once every 3 weeks, at the discretion of participants and physicians. The primary endpoint was overall survival in the intention-to-treat population. This planned analysis was triggered by reaching 470 deaths. This study is registered with ClinicalTrials.gov, NCT02446405, ANZCTR, ACTRN12614000110684, and EudraCT, 2014-003190-42. Findings Between March 31, 2014, and March 24, 2017, 1125 participants were randomly assigned to receive non-steroidal antiandrogen (n=562; control group) or enzalutamide (n=563). The median age was 69 years (IQR 63–74). This analysis was triggered on Jan 19, 2022, and an updated survival status identified a total of 476 (42%) deaths. After a median follow-up of 68 months (IQR 67–69), the median overall survival was not reached (hazard ratio 0·70 [95% CI 0·58–0·84]; p<0·0001), with 5-year overall survival of 57% (0·53–0·61) in the control group and 67% (0·63–0·70) in the enzalutamide group. Overall survival benefits with enzalutamide were consistent across predefined prognostic subgroups and planned use of concurrent docetaxel. The most common grade 3–4 adverse events were febrile neutropenia associated with docetaxel use (33 [6%] of 558 in the control group vs 37 [6%] of 563 in the enzalutamide group), fatigue (four [1%] vs 33 [6%]), and hypertension (31 [6%] vs 59 [10%]). The incidence of grade 1–3 memory impairment was 25 (4%) versus 75 (13%). No deaths were attributed to study treatment. Interpretation The addition of enzalutamide to standard of care showed sustained improvement in overall survival for patients with metastatic hormone-sensitive prostate cancer and should be considered as a treatment option for eligible patients. Funding Astellas Pharma.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
3秒前
4秒前
化学材料完成签到,获得积分10
7秒前
化学材料发布了新的文献求助10
10秒前
花花2024完成签到 ,获得积分10
11秒前
量子星尘发布了新的文献求助10
20秒前
doctorw完成签到 ,获得积分0
20秒前
CRUSADER完成签到,获得积分10
22秒前
博弈完成签到 ,获得积分10
25秒前
27秒前
蒋不惜完成签到,获得积分10
30秒前
GQ发布了新的文献求助10
34秒前
凶狠的白桃完成签到 ,获得积分10
36秒前
久晓完成签到 ,获得积分10
38秒前
xfy完成签到,获得积分10
40秒前
橙橙完成签到 ,获得积分10
40秒前
健忘的晓小完成签到 ,获得积分10
42秒前
Echo1128完成签到 ,获得积分10
43秒前
Gino完成签到,获得积分0
43秒前
满意涵梅完成签到 ,获得积分10
44秒前
DDDazhi完成签到,获得积分0
44秒前
46秒前
量子星尘发布了新的文献求助10
49秒前
plant完成签到 ,获得积分10
54秒前
杨羕发布了新的文献求助10
56秒前
无奈完成签到,获得积分10
56秒前
乐观的星月完成签到 ,获得积分10
58秒前
谨慎的雁菡完成签到 ,获得积分10
58秒前
科研通AI6.3应助小可采纳,获得10
1分钟前
研友_LpvQlZ完成签到,获得积分10
1分钟前
量子星尘发布了新的文献求助10
1分钟前
房房不慌完成签到 ,获得积分10
1分钟前
好学的猪完成签到,获得积分10
1分钟前
郭磊完成签到 ,获得积分10
1分钟前
popo6150完成签到 ,获得积分10
1分钟前
灵巧的长颈鹿完成签到,获得积分10
1分钟前
小胖完成签到 ,获得积分10
1分钟前
1分钟前
11完成签到 ,获得积分10
1分钟前
大笨蛋完成签到 ,获得积分10
1分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 2000
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
Lloyd's Register of Shipping's Approach to the Control of Incidents of Brittle Fracture in Ship Structures 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6143382
求助须知:如何正确求助?哪些是违规求助? 7970767
关于积分的说明 16551697
捐赠科研通 5255765
什么是DOI,文献DOI怎么找? 2806294
邀请新用户注册赠送积分活动 1786919
关于科研通互助平台的介绍 1656296