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CompilationTom Lee
Although Merck and Eisai's oral multi-receptor tyrosine kinase inhibitor Lenvima has obtained a series of positive trial data over the years, the combination therapy still seems to face a difficult problem in the field of bladder cancer
Lenvima in combination with Merck's Keytruda did not significantly prolong the lives of patients with newly diagnosed advanced urothelial cancer compared with Keytruda alone, according to newly released trial results
The results of the Phase 3 LEAP-011 clinical trial were presented today at the American Society of Clinical Oncology Genitourinary System (ASCO GU) Cancer Symposium
Regarding the results of this trial, Scot Ebbinghaus, MD, head of Merck's advanced tumor clinical development therapeutic area, is optimistic that the results further consolidate the clinical application of Merck's Keytruda monotherapy in patients who are not eligible for platinum-based chemotherapy
After Merck's Keytruda previously failed to show a survival benefit in a phase 3 confirmatory trial called KEYNOTE-361, the FDA has restricted the drug's use to populations similar to those enrolled in the LEAP-011 trial
Additionally, as part of an update to the indication label, the indication was changed for the treatment of patients with locally advanced or metastatic urothelial carcinoma (mUC) who are not candidates for any platinum-containing chemotherapy regimen
Notably, this isn't the first time the Keytruda and Lenvima combination has encountered development setbacks
However, in January this year, another pivotal Phase 3 clinical trial of Keytruda and Lenvima combination therapy achieved positive data
Currently, anti-nectin-4 drugs have been previously approved for the treatment of bladder cancer
Reference source: ASCO GU: Merck, Eisai's Lenvima fails to improve on Keytruda in bladder cancer as key Padcev readout nears