Lenvatinib Plus Pembrolizumab or Everolimus for Advanced Renal Cell Carcinoma
Overview
Authors
Affiliations
Background: Lenvatinib in combination with pembrolizumab or everolimus has activity against advanced renal cell carcinoma. The efficacy of these regimens as compared with that of sunitinib is unclear.
Methods: In this phase 3 trial, we randomly assigned (in a 1:1:1 ratio) patients with advanced renal cell carcinoma and no previous systemic therapy to receive lenvatinib (20 mg orally once daily) plus pembrolizumab (200 mg intravenously once every 3 weeks), lenvatinib (18 mg orally once daily) plus everolimus (5 mg orally once daily), or sunitinib (50 mg orally once daily, alternating 4 weeks receiving treatment and 2 weeks without treatment). The primary end point was progression-free survival, as assessed by an independent review committee in accordance with Response Evaluation Criteria in Solid Tumors, version 1.1. Overall survival and safety were also evaluated.
Results: A total of 1069 patients were randomly assigned to receive lenvatinib plus pembrolizumab (355 patients), lenvatinib plus everolimus (357), or sunitinib (357). Progression-free survival was longer with lenvatinib plus pembrolizumab than with sunitinib (median, 23.9 vs. 9.2 months; hazard ratio for disease progression or death, 0.39; 95% confidence interval [CI], 0.32 to 0.49; P<0.001) and was longer with lenvatinib plus everolimus than with sunitinib (median, 14.7 vs. 9.2 months; hazard ratio, 0.65; 95% CI, 0.53 to 0.80; P<0.001). Overall survival was longer with lenvatinib plus pembrolizumab than with sunitinib (hazard ratio for death, 0.66; 95% CI, 0.49 to 0.88; P = 0.005) but was not longer with lenvatinib plus everolimus than with sunitinib (hazard ratio, 1.15; 95% CI, 0.88 to 1.50; P = 0.30). Grade 3 or higher adverse events emerged or worsened during treatment in 82.4% of the patients who received lenvatinib plus pembrolizumab, 83.1% of those who received lenvatinib plus everolimus, and 71.8% of those who received sunitinib. Grade 3 or higher adverse events occurring in at least 10% of the patients in any group included hypertension, diarrhea, and elevated lipase levels.
Conclusions: Lenvatinib plus pembrolizumab was associated with significantly longer progression-free survival and overall survival than sunitinib. (Funded by Eisai and Merck Sharp and Dohme; CLEAR ClinicalTrials.gov number, NCT02811861.).
Zhang D, Shen C, Zhang W, Chen H, Zhao J Front Immunol. 2025; 16:1524497.
PMID: 40070839 PMC: 11893867. DOI: 10.3389/fimmu.2025.1524497.
Park Y, Lee C, Seo W, Chung J, Ku J, Kim K Oncol Lett. 2025; 29(4):211.
PMID: 40070791 PMC: 11894504. DOI: 10.3892/ol.2025.14957.
Naldi L, Catalano M, Melica M, Polvani S, Papini D, Landini I Sci Rep. 2025; 15(1):8067.
PMID: 40055463 PMC: 11889168. DOI: 10.1038/s41598-025-92674-6.
Hosoi T, Yoshioka S, Hiraguri A, Kirihana Y, Koguchi T, Tamaki M IJU Case Rep. 2025; 8(2):150-153.
PMID: 40034897 PMC: 11872193. DOI: 10.1002/iju5.12830.
Papillary Renal Cell Carcinoma: Current Evidence and Future Directions.
Jang A, Hobeika C, Gupta S Kidney Cancer. 2025; 8(1):61-79.
PMID: 40027140 PMC: 11870658. DOI: 10.3233/kca-230027.