Real-life Use of Cabozantinib in Front-line therapy for Metastatic Renal Cell Carcinoma: The CabFRONT Study (Meet-URO 24)
Year: 2025
Type: article
Study design: Observational Study
Abstract: Cabozantinib is active and safe in patients with intermediate-risk or poor-risk metastatic renal cell carcinoma, and is a valid option in patients pretreated with or ineligible for immune checkpoint inhibitors. Dose reductions or modifications of the cabozantinib schedule because of toxicities do not affect outcomes. Cabozantinib remains the cornerstone for treatment of patients metastatic renal cell carcinoma (mRCC), whether pretreated with an immune-oncology (IO) agent and/or tyrosine kinase inhibitor, or treatment-naïve but ineligible for IO-based combinations. CabFRONT (Meet-URO 24) was a retrospective, observational, multicentre study of a real-life population of treatment-naïve patients with intermediate-risk or poor-risk mRCC treated with cabozantinib. A total of 211 treatment- naïve patients with intermediate- or poor-risk mRCC according to the International Metastatic RCC Database Consortium criteria were included. At median follow-up of 50.4 mo (interquartile range 46.9–53.2), median progression-free survival (PFS) was 9.1 mo (interquartile range 7.4–10.4) and median overall survival (OS) was 19.8 mo (95% confidence interval [CI] 14.1–27.0). A reduced dose was not associated with significant differences in median OS (hazard ratio [HR] 1.08, 95% CI 0.77–1.52; p = 0.7) or PFS (HR 1.25, 95% CI 0.91–1.70; p = 0.16). A modified schedule because of toxicities was also not associated with significant differences in survival or progression (HR for death 0.56, 95% CI 0.25–1.28; p = 0.16; HR for progression or death 0.88, 95% CI 0.48–1.64; p= 0.7). The objective response rate according to Response Evaluation Criteria in Solid Tumours version 1.1 was 39%. The most common grade 3 adverse events were mucositis (9%), fatigue (9%), and diarrhoea (8.5%). Front-line cabozantinib was effective and safe in an unselected real-life population of patients with intermediate-risk or poor-risk mRCC. Cabozantinib could be a choice for patients who cannot receive IO-based combinations or a speculative option for individuals with “early progression” on adjuvant IO. We looked at outcomes for patients with metastatic kidney cancer treated with an inhibitor called cabozantinib in a large European population. We found that cabozantinib is active and safe, and that changes in the dose or treatment schedule because of side effects do not affect outcomes. Cabozantinib could be an option for patients who cannot receive immunotherapy for metastatic disease.
Source: European Urology Open Science
Authors: Marco Stellato, Pierangela Sepe, Enrico Bronte, Vincenza Conteduca, Maria Cossu Rocca, Ugo De Giorgi, Marilena Di Napoli, Luca Galli, Lorena Incorvaia, Luca Lalli, Brigida Anna Maiorano, Marco Maruzzo, Alessia Mennitto, Giandomenico Roviello, Matteo Santoni, Mariella Sorarù, Elisa Zanardi, Paolo Zucali, Giuseppe Procopio, Elena Verzoni
Institutions: Fondazione IRCCS Istituto Nazionale dei Tumori, Azienda Socio Sanitaria Territoriale Santi Paolo e Carlo, Ospedale Vincenzo Cervello, University of Foggia, Ospedali Riuniti di Foggia, European Institute of Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", University of Pisa, Azienda Ospedaliera Universitaria Pisana, University of Palermo, Casa Sollievo della Sofferenza, Istituto Oncologico Veneto, Azienda Ospedaliero Universitaria Maggiore della Carita, University of Florence, Ospedale di Macerata, Ospedale Policlinico San Martino, Humanitas University, IRCCS Humanitas Research Hospital
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,800
Funders: Ipsen Biopharmaceuticals, Ipsen
OpenAlex ID: W4415219393
