About KEYTRUDA Oesophago-gastric

KEYTRUDA® (pembrolizumab) in locally advanced unresectable or metastatic oesophageal cancer

Prescribing Information [External link]

KEYTRUDA in combination with platinum and fluoropyrimidine-based chemotherapy is indicated for:

Locally advanced unresectable or metastatic oesophageal cancer
For use in
The first-line treatment of patients with locally advanced unresectable or metastatic carcinoma of the oesophagus or human epidermal growth factor receptor 2 (HER2)-negative gastroesophageal junction (GEJ) adenocarcinoma in adults whose tumours express PD-L1 Combined Positive Score (CPS) ≥10.1
Dosing schedule
The recommended dose is either 200 mg every 3 weeks or 400 mg every 6 weeks, administered as an intravenous infusion over 30 minutes1
Duration of treatment
Treat until disease progression or unacceptable toxicity1
Clinical trialKEYNOTE-590 was a Phase 3, multicentre, double-blind, active-controlled study of adult patients with locally advanced unresectable or metastatic carcinoma of the oesophagus or human epidermal growth factor receptor 2 (HER2)-negative gastroesophageal junction (GEJ) adenocarcinoma, randomised 1:1 to receive pembrolizumab + cisplatin + 5-FU (fluorouracil) or placebo + cisplatin + 5-FU1



Click here to download the KEYNOTE-590 clinical data presentation

Download

Reference

  1. KEYTRUDA Summary of Product Characteristics.

Supporting documentation

Prescribing Information [External link]
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