Abstract

Three tyrosine kinase inhibitor + immuno-oncology (TKI+IO) regimens (i.e., cabozantinib+nivolumab [C+N], axitinib+pembrolizumab [A+P], and lenvatinib+pembrolizumab [L+P]) have been approved by the Food and Drug Administration (FDA) for the first-line treatment of advanced renal cell carcinoma (aRCC). Given the limited information on costs of treating adverse events (AEs), we estimated the costs of all-cause grade 3/4 AEs for C+N, A+P, and L+P from the CheckMate 9ER, KEYNOTE-426, and CLEAR trials, respectively.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.