CYRAMZA (ramucirumab), monoclonal antibody
Reason for request
In gastric or gastro-oesophageal junction cancer:
- In combination with paclitaxel, its actual benefit is moderate
- In monotherapy, its actual benefit is insufficient to justify its reimbursement
» CYRAMZA has Marketing Authorisation in treatment of advanced gastric cancers or gastro-oesophageal junction adenocarcinoma, having progressed after platinum salt- and/or fluoropyrimidine-based chemotherapy, in combination with paclitaxel or in monotherapy when paclitaxel is not indicated.
» In combination with paclitaxel compared with paclitaxel alone, the median overall survival was slightly longer (+2.3 months) with an increase in adverse effects.
» In monotherapy, its actual benefit is insufficient to justify its reimbursement due to a negligible clinical benefit.
Clinical Benefit
Moderate |
- |
Insufficient |
Clinical Added Value
no clinical added value |
- |
Therapeutic use
- |