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 | |
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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 trial![]() | KEYNOTE-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
- KEYTRUDA Summary of Product Characteristics.
Supporting documentation
Prescribing Information [External link]
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