TY - JOUR
T1 - Activity of lenvatinib-based therapy in previously treated patients with metastatic renal cell carcinoma
T2 - A European multicenter study (LENVA-LAT)
AU - Gavira, Javier
AU - Auclin, Edouard
AU - Rey-Cardenas, Macarena
AU - Roy, Pritha
AU - Tapia, Jose C.
AU - Nay, Paula
AU - Vinceneux, Armelle
AU - Lefort, Felix
AU - Nannini, Simon
AU - Randis, Adela Maria del Carmen
AU - Naoun, Natacha
AU - Escudier, Bernard
AU - Borchiellini, Delphine
AU - de Velasco, Guillermo
AU - Barthelemy, Philippe
AU - Gross-Goupil, Marine
AU - Negrier, Sylvie
AU - Oudard, Stéphane
AU - Frazer, Ricky D.
AU - Albiges, Laurence
AU - Flippot, Ronan
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/5/2
Y1 - 2025/5/2
N2 - Background and Objective: Lenvatinib's activity after immune checkpoint inhibitors (ICI) combination therapy in renal cell carcinoma (RCC) remains unknown. We aimed to describe the real-world outcomes of patients with metastatic RCC (mRCC) treated with lenvatinib after failure of the prior standard of care. Methods: Multicenter retrospective study including patients with mRCC treated with lenvatinib-based therapies beyond first-line therapy between 2020 and 2024. The primary endpoints were objective response rate (ORR) and time-to-treatment failure (TTF). Secondary endpoints included disease control rate (DCR), overall survival (OS), and safety. Results: We included 133 patients, with a median age of 61 years. Clear-cell was the main subtype (82.0 %). Before lenvatinib treatment, 15.8 %, 51.9 %, and 27.8 % of patients showed favorable, intermediate, and poor risk disease, respectively, according to the International Metastatic RCC Database Consortium (IMDC). Moreover, patients received a median of 3 previous lines of treatment, including ICIs (90.2 %) and cabozantinib (90.2 %). Lenvatinib was given alone (45.9 %) or in combination with everolimus (33.8 %), pembrolizumab (18.0 %) or investigational agents (2.3 %). The ORR and DCR were 29.1 % and 67.7 %, respectively, with no differences between regimens or lines of treatment. With a median follow-up time of 13.5 months, the median TTF and OS were 6.2 and 9.6 months. Toxicity was manageable with dose modifications required in 34.6 %. The discontinuation rate was 9.8 %, with one toxic death. Conclusion: Lenvatinib-based regimens were active and safe for heavily pre-treated patients with mRCC. These findings provide evidence to support its use in daily practice.
AB - Background and Objective: Lenvatinib's activity after immune checkpoint inhibitors (ICI) combination therapy in renal cell carcinoma (RCC) remains unknown. We aimed to describe the real-world outcomes of patients with metastatic RCC (mRCC) treated with lenvatinib after failure of the prior standard of care. Methods: Multicenter retrospective study including patients with mRCC treated with lenvatinib-based therapies beyond first-line therapy between 2020 and 2024. The primary endpoints were objective response rate (ORR) and time-to-treatment failure (TTF). Secondary endpoints included disease control rate (DCR), overall survival (OS), and safety. Results: We included 133 patients, with a median age of 61 years. Clear-cell was the main subtype (82.0 %). Before lenvatinib treatment, 15.8 %, 51.9 %, and 27.8 % of patients showed favorable, intermediate, and poor risk disease, respectively, according to the International Metastatic RCC Database Consortium (IMDC). Moreover, patients received a median of 3 previous lines of treatment, including ICIs (90.2 %) and cabozantinib (90.2 %). Lenvatinib was given alone (45.9 %) or in combination with everolimus (33.8 %), pembrolizumab (18.0 %) or investigational agents (2.3 %). The ORR and DCR were 29.1 % and 67.7 %, respectively, with no differences between regimens or lines of treatment. With a median follow-up time of 13.5 months, the median TTF and OS were 6.2 and 9.6 months. Toxicity was manageable with dose modifications required in 34.6 %. The discontinuation rate was 9.8 %, with one toxic death. Conclusion: Lenvatinib-based regimens were active and safe for heavily pre-treated patients with mRCC. These findings provide evidence to support its use in daily practice.
KW - Efficacy
KW - Kidney cancer
KW - Later lines
KW - Lenvatinib
KW - Outcomes
KW - Real-world data
KW - Renal Cell Carcinoma
KW - Safety
UR - http://www.scopus.com/inward/record.url?scp=105001694322&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2025.115389
DO - 10.1016/j.ejca.2025.115389
M3 - Article
AN - SCOPUS:105001694322
SN - 0959-8049
VL - 220
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 115389
ER -