Keytruda Adjuvant Kidney Cancer Data Cement The Future Of IO

“Practice Changing” KEYNOTE-564 Data Presented At ASCO Plenary

The data illustrate the growing importance of adjuvant settings of solid tumors for PD-1/PD-L1 inhibitors, which could make up more than one-quarter of their sales in 2025.

Human kidney on scientific background. 3d illustration
Merck & Co. presents "practice changing" data on Keytruda in adjuvant renal cell carcinoma • Source: Shutterstock

The KEYNOTE-564 study supporting use of Merck & Co., Inc.’s Keytruda(pembrolizumab) in adjuvant renal cell carcinoma (RCC), and likely another first-to-market advantage for the PD-1 inhibitor, is an important advance as checkpoint inhibitor immuno-oncology shifts to earlier use in adjuvant settings in various cancers.

The Kenilworth, NJ-based drug maker presented positive data from the Phase III KEYNOTE-564 study comparing Keytruda with placebo in adjuvant RCC at the 6 June plenary session of the American Society of Clinical Oncology annual meeting, following an earlier topline release noting that the trial showed a disease-free survival benefit. (Also see "Merck & Co.’s Keytruda Stakes Another Adjuvant Flag, In RCC" - Scrip, 8 April, 2021

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