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DOI 10.1016/j.annonc.2025.10.009

Медицинская библиотека · Annals of oncology : official journal of the European Society for Medical Oncology · 2025

A multicenter randomized phase II trial of lenvatinib plus everolimus versus cabozantinib in patients with metastatic clear-cell RCC that progressed on PD-1 immune checkpoint inhibition (LenCabo).

Hahn A W, Chahoud J, Skelton W P, Yuan Y, Zurita-Saavedra A J, Kovitz C, Alhalabi O, Campbell M T, Jonasch E, Lin J K, Desai M, Santos M J M N, Hwang H, Corn P G, Msaouel P, Tannir N M

СтатьяРандомизированное исследованиеКлиническое исследование II фазыМногоцентровое исследованиеСравнительное исследованиеПеревод в очереди

Аннотация

BACKGROUND

First-line treatments for metastatic clear-cell renal-cell carcinoma (ccRCC) combine programmed cell death protein 1 (PD-1) immune checkpoint inhibition (ICI) with cytotoxic T-lymphocyte associated protein 4 ICI or angiogenesis targeted therapies (TT). Upon progression, common options include cabozantinib or lenvatinib + everolimus, although these regimens have never been directly compared. We hypothesized that lenvatinib + everolimus will improve progression-free survival (PFS) compared with cabozantinib after progression on PD-1 ICI.

PATIENTS AND

METHODS

This multicenter, randomized phase II trial enrolled patients with metastatic ccRCC previously treated with one to two lines including PD-1 ICI. Participants received lenvatinib 18 mg/day + everolimus 5 mg/day versus cabozantinib 60 mg/day, stratified by International Metastatic RCC Database Consortium risk group and prior TT. A Bayesian optimal phase II design was used.

RESULTS

In total 90 patients were randomized; 86 patients received at least one dose of assigned lenvatinib + everolimus (n = 40) or cabozantinib (n = 46). Median time from randomization to data cut-off date (1 August 2025) was 20 months (interquartile range 14.9-22.5 months). A total of 60 PFS events were observed. Median PFS was 15.7 months with lenvatinib + everolimus and 10.2 months with cabozantinib [hazard ratio 0.51, 95% confidence interval (CI) 0.29-0.89, P = 0.02]. The objective response rate was 52.6% with lenvatinib + everolimus and 38.6% with cabozantinib. Overall survival (OS) data were immature and inconclusive due to a low number of events (n = 24/86; 1-year OS probability 87.0% versus 84.6% [95% CI 0.47% to 2.38%] with lenvatinib + everolimus versus cabozantinib, respectively. Discontinuation rates due to toxicity were 20% with lenvatinib + everolimus and 10.9% with cabozantinib.

CONCLUSIONS

In this randomized phase II trial in metastatic ccRCC that progressed on prior PD-1 ICIs, lenvatinib + everolimus significantly prolonged PFS over cabozantinib. As the first head-to-head comparison of contemporary second-line or later treatments after ICI, these results are relevant to treatment sequencing and inform oncology practice.

Для цитирования: Hahn A W, Chahoud J, Skelton W P, Yuan Y, Zurita-Saavedra A J, Kovitz C, Alhalabi O, Campbell M T, Jonasch E, Lin J K, Desai M, Santos M J M N, Hwang H, Corn P G, Msaouel P, Tannir N M. A multicenter randomized phase II trial of lenvatinib plus everolimus versus cabozantinib in patients with metastatic clear-cell RCC that progressed on PD-1 immune checkpoint inhibition (LenCabo).. Annals of oncology : official journal of the European Society for Medical Oncology. 2025. DOI: 10.1016/j.annonc.2025.10.009.

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