Keytruda-based triplet improves survival rates in cervical cancer

20 July 2023

New data from Merck & Co (NYSE: MRK) will help push its flagship immunotherapy Keytruda (pembrolizumab) into earlier lines of treatment in cervical cancer.

In 2021 the US Food and Drug Administration approved the checkpoint blocker for use as a first-line therapy, together with chemo, for what is one of the most widespread types of cancer in women.

Now, data from the Phase III KEYNOTE-A18 trial show the use of Keytruda, chemotherapy and external beam radiotherapy (EBRT) can significantly improve progression-free survival (PFS) rates.

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