Archived: cetuximab (Erbitux)
Advice
Following a full submission
cetuximab (Erbitux) is not recommended for use within NHS Scotland for the treatment of patients with epidermal growth factor receptor (EGFR)-expressing, KRAS wild-type metastatic colorectal cancer in combination with chemotherapy.
Outcomes for patients with KRAS wild-type disease were derived from retrospective, post hoc analyses of one phase ll and one phase lll study. Both these analyses showed an increase in overall response rate and a small, but statistically significant, increase in median progression free survival time when cetuximab was added to standard first-line chemotherapy.
The manufacturer did not present a sufficiently robust economic analysis to gain acceptance by SMC. The licence holder has indicated their intention to resubmit
Drug Details
| Drug Name: | cetuximab (Erbitux) |
|---|---|
| SMC Drug ID: | 543/09 |
| Manufacturer: | Merck Serono Ltd |
| Indication: | Epidermal growth factor receptor (EGFR)-expressing, KRAS wild-type metastatic colorectal cancer |
| BNF Category: | |
| Sub Category: | 8.1 Cytotoxic drugs |
| Submission Type: | Full submission |
| Status: | Not Recommended |
| Date Advice Published: | 14 April 2009 |
Current Advice
| cetuximab (Erbitux) | Resubmission | 8 February 2010 |