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Effect of systemic therapies or best supportive care after disease progression to both nivolumab and cabozantinib in metastatic renal cell carcinoma: The Meet‐Uro 19BEYOND study

Authors :
Giandomenico Roviello
Elisabetta Gambale
Roberta Giorgione
Daniele Santini
Marco Stellato
Giuseppe Fornarini
Sara Elena Rebuzzi
Umberto Basso
Davide Bimbatti
Laura Doni
Gabriella Nesi
Melissa Bersanelli
Sebastiano Buti
Ugo De Giorgi
Luca Galli
Andrea Sbrana
Raffaele Conca
Claudia Carella
Emanuele Naglieri
Sandro Pignata
Giuseppe Procopio
Lorenzo Antonuzzo
Source :
Cancer Medicine, Vol 11, Iss 16, Pp 3084-3092 (2022)
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Abstract Background Nivolumab and cabozantinib are currently approved agents in metastatic renal cell carcinoma (mRCC) but there are no data available for patients progressing to both treatments. The aim of this study was to compare active therapeutic options and best supportive care (BSC) after progression to nivolumab and cabozantinib in mRCC. Methods In this retrospective study, we selected 50 patients from eight Italian centers. The primary endpoint of the study was the overall survival (OS) of patients on active treatment versus BSC. Secondary endpoints were the progression‐free survival (PFS) and objective response rate (ORR). The efficacy of active therapy was also investigated. Results After progression to both nivolumab and cabozantinib, 57.1% of patients were given active treatment (mainly everolimus and sorafenib) while 42.9% received BSC. The median OS was 13 months (95% CI: 4‐NR) in actively treated patients and 3 months (95% CI: 2–4) in BSC patients (p = 0.001). Patients treated with sorafenib had better disease control than those treated with everolimus (stable disease: 71.4% vs. 16.7%, progression disease: 14.3% vs. 58.3%; p = 0.03), with no significant differences in PFS (5 and 3 months, 95% CI: 1–6 vs. 2–5; p = 0.6) and OS (12 and 4 months, 95% CI: 3‐NR vs. 2‐NR; p = 0.2). Conclusion After treatment with both nivolumab and cabozantinib, the choice of a safe active systemic therapy offered better outcomes than BSC.

Details

Language :
English
ISSN :
20457634
Volume :
11
Issue :
16
Database :
Directory of Open Access Journals
Journal :
Cancer Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.5c1b0d246d484bad81a6a45b350d5ccd
Document Type :
article
Full Text :
https://doi.org/10.1002/cam4.4681