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Keytruda wins FDA approval in head and neck cancer

June 12, 2019 / Anna Smith

MSD’s blockbuster cancer drug Keytruda (pembrolizumab) has won approval from the US Food and Drug Administration (FDA) to treat a type of head and neck cancer. It was approved in the Indication of first-line treatment of patients with metastatic or with unresectable, recurrent head and neck squamous cell carcinoma as monotherapy for patients whose tumours express PD-L1 or in combination with platinum and fluorouracil (FU) regardless of PD-L1 expression. The approval is based on results from the pivotal Phase 3 KEYNOTE-048 trial, where Keytruda demonstrated a significant improvement in overall survival (OS) compared with the current standard of care, the EXTREME regimen which consists of cetuximab with carboplatin or cisplatin plus FU. The results mean that the drug is the first anti-PD-1 therapy approved in the first-line setting as monotherapy in patients whose tumours express PD-L1, and also  the first anti-PD-1 therapy to demonstrate a statistically significant improvemen...