erlotinib (Tarceva)
Advice
following a full submission
erlotinib (Tarceva®) is accepted for use within NHS Scotland.
Indication under review: first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) activating mutations.
In patients with advanced or metastatic NSCLC with EGFR mutations, erlotinib was associated with significantly improved progression-free survival compared with platinum-based doublet chemotherapy regimens. There are no mature overall survival data.
This SMC advice takes account of the benefits of a Patient Access Scheme (PAS) that improves the cost-effectiveness of erlotinib. This SMC advice is contingent upon the continuing availability of the PAS in NHS Scotland.
Drug Details
| Drug Name: | erlotinib (Tarceva) |
|---|---|
| SMC Drug ID: | 749/11 |
| Manufacturer: | Roche |
| Indication: | First line treatment for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating EGFR |
| BNF Category: | |
| Sub Category: | 8.1 Cytotoxic drugs |
| Submission Type: | Full submission |
| Status: | Accepted |
| Date Advice Published: | 16 January 2012 |