LITESPARK-012: pembrolizumab plus lenvatinib with or without belzutifan or quavonlimab for advanced renal cell carcinoma

被引:3
作者
Choueiri, Toni K. [1 ,2 ]
Powles, Thomas [3 ,4 ]
Voss, Martin H. [5 ]
Plimack, Elizabeth R. [6 ]
Gurney, Howard [7 ,8 ]
Song, Yue [9 ]
Perini, Rodolfo F. [9 ]
Rodriguez-Lopez, Karla [9 ]
Rini, Brian, I [10 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02215 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Barts Hlth NHS Trust, London, England
[4] Queen Mary Univ London, Royal Free NHS Fdn Trust, Barts Canc Inst, London, England
[5] Mem Sloan Kettering Canc Ctr, New York, NY USA
[6] Fox Chase Canc Ctr, Philadelphia, PA USA
[7] Westmead Hosp, Sydney, NSW, Australia
[8] Macquarie Univ Hosp, Sydney, NSW, Australia
[9] Merck & Co Inc, Rahway, NJ USA
[10] Vanderbilt Ingram Canc Ctr, Nashville, TN USA
关键词
clear cell renal cell carcinoma; CTLA-4; inhibitor; HIF-2 alpha inhibitor; immune checkpoint inhibitor; PD-1/L1; VEGFR-TKI; NIVOLUMAB; SUNITINIB; CANCER; CABOZANTINIB; COMBINATION; EFFICACY; BLOCKADE; SAFETY;
D O I
10.2217/fon-2023-0283
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Combination treatment with immunotherapy agents and/or vascular endothelial growth factor tyrosine kinase inhibitors are a standard of care for patients with advanced clear cell renal cell carcinoma (ccRCC). Novel therapeutic combinations that include the hypoxia-inducible factor 2 alpha inhibitor belzutifan and the cytotoxic T-lymphocyte-associated protein 4 inhibitor quavonlimab are being investigated for their potential to further improve patient outcomes. This protocol describes the rationale and design of the randomized, phase III LITESPARK-012 study, which will evaluate the efficacy and safety of pembrolizumab plus lenvatinib with or without belzutifan or quavonlimab as first-line treatment for advanced ccRCC. Results from this study may support triplet combination therapies as a potential new standard of care for advanced ccRCC.
引用
收藏
页码:2631 / 2640
页数:10
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