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Lenvatinib plus Pembrolizumab or Everolimus for Advanced Renal Cell Carcinoma

Authors
 Robert Motzer  ;  Boris Alekseev  ;  Sun-Young Rha  ;  Camillo Porta  ;  Masatoshi Eto  ;  Thomas Powles  ;  Viktor Grünwald  ;  Thomas E Hutson  ;  Evgeny Kopyltsov  ;  María J Méndez-Vidal  ;  Vadim Kozlov  ;  Anna Alyasova  ;  Sung-Hoo Hong  ;  Anil Kapoor  ;  Teresa Alonso Gordoa  ;  Jaime R Merchan  ;  Eric Winquist  ;  Pablo Maroto  ;  Jeffrey C Goh  ;  Miso Kim  ;  Howard Gurney  ;  Vijay Patel  ;  Avivit Peer  ;  Giuseppe Procopio  ;  Toshio Takagi  ;  Bohuslav Melichar  ;  Frederic Rolland  ;  Ugo De Giorgi  ;  Shirley Wong  ;  Jens Bedke  ;  Manuela Schmidinger  ;  Corina E Dutcus  ;  Alan D Smith  ;  Lea Dutta  ;  Kalgi Mody  ;  Rodolfo F Perini  ;  Dongyuan Xing  ;  Toni K Choueiri 
Citation
 NEW ENGLAND JOURNAL OF MEDICINE, Vol.384(14) : 1289-1300, 2021-04 
Journal Title
NEW ENGLAND JOURNAL OF MEDICINE
ISSN
 0028-4793 
Issue Date
2021-04
MeSH
Adult ; Aged ; Aged, 80 and over ; Antibodies, Monoclonal, Humanized / administration & dosage* ; Antibodies, Monoclonal, Humanized / adverse effects ; Antineoplastic Agents / adverse effects ; Antineoplastic Agents / therapeutic use ; Antineoplastic Combined Chemotherapy Protocols / adverse effects ; Antineoplastic Combined Chemotherapy Protocols / therapeutic use* ; Carcinoma, Renal Cell / drug therapy* ; Carcinoma, Renal Cell / mortality ; Everolimus / administration & dosage* ; Everolimus / adverse effects ; Female ; Humans ; Kidney Neoplasms / drug therapy* ; Kidney Neoplasms / mortality ; Male ; Middle Aged ; Phenylurea Compounds / administration & dosage* ; Phenylurea Compounds / adverse effects ; Programmed Cell Death 1 Receptor / antagonists & inhibitors* ; Progression-Free Survival ; Protein Kinase Inhibitors / therapeutic use ; Quinolines / administration & dosage* ; Quinolines / adverse effects ; Sunitinib / adverse effects ; Sunitinib / therapeutic use ; Survival Analysis
Abstract
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.).
Full Text
https://www.nejm.org/doi/10.1056/NEJMoa2035716
DOI
10.1056/NEJMoa2035716
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Rha, Sun Young(라선영) ORCID logo https://orcid.org/0000-0002-2512-4531
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/185460
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