Pembrolizumab plus axitinib versus sunitinib as first-line therapy for advanced clear cell renal cell carcinoma: 5-year analysis of KEYNOTE-426.

医学 肾细胞癌 替西罗莫司 人口 彭布罗利珠单抗 内科学 舒尼替尼 中期分析 中止 肿瘤科 泌尿科 临床试验 癌症 细胞凋亡 生物化学 化学 蛋白激酶B 环境卫生 免疫疗法 mTOR抑制剂的发现与发展
作者
Brian I. Rini,Elizabeth R. Plimack,V.P. Stus,Rustem Gafanov,Tom Waddell,Dmitry Nosov,Frédéric Pouliot,B. Yа. Alekseev,Denis Soulières,Bohuslav Melichar,Ihor Vynnychenko,Sérgio Jobim Azevedo,Delphine Borchiellini,Ray McDermott,Jens Bedke,Satoshi Tamada,Sterling Wu,Joseph E. Burgents,L. Rhoda Molife,Thomas Powles
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:41 (17_suppl): LBA4501-LBA4501 被引量:50
标识
DOI:10.1200/jco.2023.41.17_suppl.lba4501
摘要

LBA4501 Background: At the first interim analysis of the randomized, open-label, phase 3 KEYNOTE-426 (NCT02853331) study, 1L pembro + axi showed statistically significant OS, PFS, and ORR over sun for advanced ccRCC. We report results with 5-y minimum follow-up. Methods: Adults with confirmed locally advanced or metastatic ccRCC with or without sarcomatoid features, no previous systemic therapy for metastatic ccRCC, KPS ≥70%, and ≥1 lesion measurable per RECIST v1.1 were randomly assigned 1:1 to receive pembro 200 mg IV Q3W for 35 doses (~2 y) + axi 5 mg PO BID or sun 50 mg PO QD on a 4-wk-on/2-wk-off schedule. Dual primary end points were OS and PFS per RECIST v1.1 by blinded independent central review (BICR). Secondary end points included ORR and DOR per RECIST v1.1 by BICR, and safety. A post hoc analysis adjusting for the effect of subsequent therapy on OS using a 2-stage adjustment model was conducted. Results: Of 861 enrolled patients (pts), 432 were assigned to pembro + axi and 429 to sun. Median study follow-up was 67.2 mo (range, 60.0-75.0). Efficacy for the ITT population and IMDC risk subgroups are shown in table. For pembro + axi vs sun, the 60-mo OS rates were 41.9% vs 37.1%, and the 60-mo PFS rates were 18.3% vs 7.3%. Median DOR (range) was 23.6 mo (1.4+ to 68.6+) for pembro + axi and 15.3 mo (2.3-68.3) for sun. In pts who discontinued treatment, 237/381 pts (62.2%) in the pembro + axi arm and 300/406 pts (73.9%) in the sun arm received subsequent anticancer treatment. The HR for OS when adjusted for subsequent therapy was 0.67 (95% CI, 0.52-0.84). Clinical data on pts who completed 2 y of pembro will be presented. No new safety signals were observed. Conclusions: After 5 y of follow-up, pembro + axi had sustained OS, PFS, and ORR benefits over sun in advanced ccRCC. These results are the longest follow-up to date of an anti–PD-1/L1 inhibitor + VEGFR TKI in this pt population and continue to support the use of pembro + axi as a 1L standard of care for advanced ccRCC. Clinical trial information: NCT02853331 .

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
自由曼冬完成签到 ,获得积分10
刚刚
1秒前
3秒前
3秒前
4秒前
5秒前
jielo发布了新的文献求助10
5秒前
端庄夏青完成签到,获得积分10
5秒前
6秒前
怡然新之完成签到 ,获得积分10
8秒前
8秒前
8秒前
学术小垃圾发布了新的文献求助100
8秒前
123发布了新的文献求助10
9秒前
彭于晏应助YOKO采纳,获得10
10秒前
科研通AI6.4应助火山书痴采纳,获得30
11秒前
Whisper发布了新的文献求助10
11秒前
lalalla发布了新的文献求助10
11秒前
12秒前
12秒前
清嘉发布了新的文献求助10
13秒前
14秒前
呼呼完成签到,获得积分10
15秒前
QQQ123完成签到,获得积分10
15秒前
刘刘球完成签到,获得积分10
17秒前
18秒前
CipherSage应助杨小洋采纳,获得10
18秒前
酷波er应助naplzp采纳,获得30
18秒前
呼呼发布了新的文献求助20
19秒前
白玲发布了新的文献求助10
19秒前
wangyumumu完成签到,获得积分10
20秒前
youth应助请叫我女侠采纳,获得50
20秒前
QQQ123发布了新的文献求助10
20秒前
21秒前
斯文败类应助专注向真采纳,获得10
22秒前
24秒前
万能图书馆应助lanxin采纳,获得10
24秒前
25秒前
顾矜应助星先生采纳,获得10
25秒前
WMT完成签到 ,获得积分10
26秒前
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
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场现状调查及投资机会研判报告 1000
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场规模及竞争格局分析报告 1000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
适配Micro-LED色转换的高兼容性量子点负性光刻胶制备与工艺研究 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7316632
求助须知:如何正确求助?哪些是违规求助? 8932628
关于积分的说明 18936046
捐赠科研通 6976622
什么是DOI,文献DOI怎么找? 3214079
关于科研通互助平台的介绍 2382025
邀请新用户注册赠送积分活动 2192830