In the open-label phase 2 LITESPARK-003 study, led by Dana-Farber Cancer Institute’s Toni Choueiri, MD, researchers investigated for the first time the combination of cabozantinib, an anti-angiogenic agent, plus belzutifan, a first-in-class HIF-2α inhibitor. The findings are published in The Lancet Oncology journal.
The researchers previously reported results for cohort 2 of the trial, which includes patients previously treated with immunotherapy. This study reports results for cohort 1, which includes patients who have not yet received treatment for advanced kidney cancer.
After a median follow up of 24 months, 70% of patients had a confirmed objective response, with 4 of 50 patients experiencing a complete response and 31 of 50 experiencing a partial response. Seven of the 50 patients had serious treatment-related adverse events, though they were manageable.
Current first-line treatment for advanced clear-cell renal cell carcinoma includes anti-PD1 or anti-PD-L1 immunotherapy in combination with a CTLA-4 inhibitor or a VEGF tyrosine kinase inhibitor such as cabozantanib. These options have improved outcomes in patients; however, not all patients respond, and some responses do not last. This study’s results suggest that further investigation of this novel combination as first-line therapy option is warranted.
More information:
Toni K Choueiri et al, Belzutifan plus cabozantinib as first-line treatment for patients with advanced clear-cell renal cell carcinoma (LITESPARK-003): an open-label, single-arm, phase 2 study, The Lancet Oncology (2025). DOI: 10.1016/S1470-2045(24)00649-1
Citation:
Phase 2 results suggest continued study of novel first-line combo for advanced kidney cancer (2025, January 17)
retrieved 17 January 2025
from https://medicalxpress.com/news/2025-01-phase-results-line-combo-advanced.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.
In the open-label phase 2 LITESPARK-003 study, led by Dana-Farber Cancer Institute’s Toni Choueiri, MD, researchers investigated for the first time the combination of cabozantinib, an anti-angiogenic agent, plus belzutifan, a first-in-class HIF-2α inhibitor. The findings are published in The Lancet Oncology journal.
The researchers previously reported results for cohort 2 of the trial, which includes patients previously treated with immunotherapy. This study reports results for cohort 1, which includes patients who have not yet received treatment for advanced kidney cancer.
After a median follow up of 24 months, 70% of patients had a confirmed objective response, with 4 of 50 patients experiencing a complete response and 31 of 50 experiencing a partial response. Seven of the 50 patients had serious treatment-related adverse events, though they were manageable.
Current first-line treatment for advanced clear-cell renal cell carcinoma includes anti-PD1 or anti-PD-L1 immunotherapy in combination with a CTLA-4 inhibitor or a VEGF tyrosine kinase inhibitor such as cabozantanib. These options have improved outcomes in patients; however, not all patients respond, and some responses do not last. This study’s results suggest that further investigation of this novel combination as first-line therapy option is warranted.
More information:
Toni K Choueiri et al, Belzutifan plus cabozantinib as first-line treatment for patients with advanced clear-cell renal cell carcinoma (LITESPARK-003): an open-label, single-arm, phase 2 study, The Lancet Oncology (2025). DOI: 10.1016/S1470-2045(24)00649-1
Citation:
Phase 2 results suggest continued study of novel first-line combo for advanced kidney cancer (2025, January 17)
retrieved 17 January 2025
from https://medicalxpress.com/news/2025-01-phase-results-line-combo-advanced.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.