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
香蕉觅云应助xmm11_AMJ采纳,获得10
刚刚
1秒前
念安完成签到,获得积分10
1秒前
1秒前
嘟嘟嘟完成签到,获得积分10
3秒前
傲娇若南发布了新的文献求助10
3秒前
田様应助倍他乐克采纳,获得10
3秒前
彩霞发布了新的文献求助10
3秒前
Shawn完成签到,获得积分10
3秒前
科研通AI6.2应助永恒采纳,获得10
4秒前
ccc发布了新的文献求助10
4秒前
aaa完成签到,获得积分10
4秒前
5秒前
6秒前
6秒前
7秒前
王友发布了新的文献求助10
7秒前
赵祥宇发布了新的文献求助10
8秒前
华仔应助black采纳,获得10
8秒前
Golden完成签到,获得积分10
8秒前
9秒前
天天快乐应助曾经的云朵采纳,获得10
9秒前
awaer完成签到,获得积分10
9秒前
嘟嘟嘟发布了新的文献求助30
11秒前
xuejingling发布了新的文献求助10
11秒前
11秒前
12秒前
raner完成签到 ,获得积分10
13秒前
CCCCCL完成签到,获得积分10
13秒前
black完成签到,获得积分10
13秒前
深情安青应助王友采纳,获得10
14秒前
15秒前
泡芙2完成签到 ,获得积分10
16秒前
16秒前
17秒前
Xsterm完成签到 ,获得积分10
17秒前
ale应助有我ID随机吗采纳,获得10
18秒前
18秒前
王文韬完成签到,获得积分10
18秒前
学无止境发布了新的文献求助10
19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
Geist der Kunst und Kultur 1000
Social Psychology in the Real World 800
Resistance Spot Welding Dataset for Automobile Body-in-White Quality Analysis 748
悉尼大学博士学位论文,题目:Modelling and testing of one-sided stitched laminated composites. 作者:Kristopher P. Plain 700
Machine Learning for Asset Management and Pricing 600
Numerical analysis of the coupled atmosphere-ocean models (CAO II). II 600
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 7411049
求助须知:如何正确求助?哪些是违规求助? 9015164
关于积分的说明 19201917
捐赠科研通 7043135
什么是DOI,文献DOI怎么找? 3233353
关于科研通互助平台的介绍 2395571
邀请新用户注册赠送积分活动 2215388