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

Author:

Choueiri Toni K1ORCID,Powles Thomas2,Voss Martin H3,Plimack Elizabeth R4,Gurney Howard56,Song Yue7,Perini Rodolfo F7,Rodriguez-Lopez Karla7,Rini Brian I8

Affiliation:

1. Dana-Farber Cancer Institute & Harvard Medical School, Boston, MA, USA

2. Barts Health NHS Trust & the Royal Free NHS Foundation Trust, Barts Cancer Institute, Queen Mary University of London, London, UK

3. Memorial Sloan Kettering Cancer Center, New York, NY, USA

4. Fox Chase Cancer Center, Philadelphia, PA, USA

5. Westmead Hospital, Sydney, NSW, Australia

6. Macquarie University Hospital, Sydney, NSW, Australia

7. Merck & Co., Inc., Rahway, NJ, USA

8. Vanderbilt-Ingram Cancer Center, Nashville, TN, USA

Abstract

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 2α 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. Clinical trial registry: NCT04736706 ( ClinicalTrials.gov )

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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