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Characterization of Responses to Lenvatinib plus Pembrolizumab in Patients with Advanced Renal Cell Carcinoma at the Final Prespecified Survival Analysis of the Phase 3 CLEAR Study

Authors
 Motzer, Robert J.  ;  Choueiri, Toni K.  ;  Hutson, Thomas  ;  Rha, Sun Young  ;  Puente, Javier  ;  Lalani, Aly-Khan A.  ;  Winquist, Eric  ;  Eto, Masatoshi  ;  Basappa, Naveen S.  ;  Tannir, Nizar M.  ;  Vaishampayan, Ulka  ;  Bjarnason, Georg A.  ;  Oudard, Stephane  ;  Gruenwald, Viktor  ;  Burgents, Joseph  ;  Xie, Ran  ;  McKenzie, Jodi  ;  Powles, Thomas 
Citation
 EUROPEAN UROLOGY, Vol.86(1) : 4-9, 2024-07 
Journal Title
EUROPEAN UROLOGY
ISSN
 0302-2838 
Issue Date
2024-07
Keywords
Renal cell carcinoma ; Lenvatinib plus pembrolizumab ; Lenvatinib ; Pembrolizumab
Abstract
In the phase 3 CLEAR trial, lenvatinib plus pembrolizumab (L + P) showed superior efficacy versus sunitinib in treatment-na & iuml;ve patients with advanced renal cell carcinoma (aRCC). The combination treatment was associated with a robust objective response rate of 71%. Here we report tumor responses for patients in the L + P arm in CLEAR, with median follow-up of 4 yr at the final prespecified overall survival (OS) analysis. Tumor responses were assessed by independent review using Response Evaluation Criteria in Solid Tumors v1.1. Patients with a complete response (CR; n = 65), partial response (PR) with maximum tumor shrinkage >= 75% (near-CR; n = 59), or PR with maximum tumor shrinkage <75% (other PR; n = 129), were characterized in terms of their baseline characteristics. The median duration of response was 43.7 mo (95% confidence interval [CI] 39.2-not estimable) for the CR group, 30.5 mo (95% CI 22.4-not estimable) for the near-CR group, and 17.2 mo (95% CI 12.5-21.4) for the other PR group. The 36-mo OS rates were consistently high in the CR (97%), near-CR (86%), and other PR (62%) groups. Robust objective response rates were observed across International Metastatic RCC Database Consortium favorable-risk (69%, 95% CI 60-78%), intermediate-risk (73%, 95% CI 67-79%), and poor-risk (70%, 95% CI 54-85%) subgroups. The robust response to L + P supports this combination as a standard-of-care first-line treatment for patients with aRCC.
DOI
10.1016/j.eururo.2024.03.015
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/22282913/200456
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