BRAF in non-small cell lung cancer
4 EU-approved indications in non-small cell lung cancer need a BRAF result: encorafenib (advanced), trametinib (advanced), dabrafenib (advanced) and binimetinib (advanced).
Line of therapy
| Drug | Biomarker requirement | Regimen | Setting | Conditions |
|---|---|---|---|---|
| BRAF mutation4 | ||||
Mektovi | V600E | + encorafenib | Any line advanced | None |
Tafinlar | V600 | + trametinib | Any line advanced | None |
Braftovi | V600E | + binimetinib | Any line advanced | None |
Mekinist | V600 | + dabrafenib | Any line advanced | None |
16 approvals for NSCLC need no biomarker and apply whatever the result. All approvals for NSCLC
See also
Label wording4
The sentence from section 4.1 of the SmPC that each indication above comes from.
- Encorafenib (Braftovi)
Encorafenib in combination with binimetinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a BRAF V600E mutation.
- Trametinib (Mekinist)
Trametinib in combination with dabrafenib is indicated for the treatment of adults with advanced non-small cell lung cancer with a BRAF V600 mutation.
- Dabrafenib (Tafinlar)
Dabrafenib in combination with trametinib is indicated for the treatment of adults with advanced non-small cell lung cancer with a BRAF V600 mutation.
- Binimetinib (Mektovi)
Binimetinib in combination with encorafenib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a BRAF V600E mutation.