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BRAF V600E (and V600K) in cutaneous melanoma is the prototypical driver: combination BRAF...

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDBMA-BRAF-V600E-MELANOMA
TypeActionability
Statusreviewed 2026-04-27 | pending_clinical_signoff | actionability review required
DiseasesDIS-MELANOMA
SourcesSRC-CIVIC SRC-ESMO-MELANOMA-2024 SRC-NCCN-MELANOMA-2025

Actionability Facts

BiomarkerBIO-BRAF-V600E
VariantV600E
DiseaseDIS-MELANOMA
ESCAT tierIA
Recommended combinationsdabrafenib + trametinib, encorafenib + binimetinib, vemurafenib + cobimetinib, atezolizumab + vemurafenib + cobimetinib (triplet)
Contraindicated monotherapyBRAFi monotherapy (vemurafenib alone) — inferior OS vs combo, paradoxical RAS/RAF activation in BRAF-WT clones
Evidence summaryBRAF V600E (and V600K) in cutaneous melanoma is the prototypical driver: combination BRAF + MEK inhibition (dabrafenib + trametinib; encorafenib + binimetinib; vemurafenib + cobimetinib) yields high ORR (~65-70%) and improves OS vs single-agent BRAFi (COMBI-d/v, coBRIM, COLUMBUS). Adjuvant dabrafenib + trametinib improves RFS in resected stage III (COMBI-AD). Triplet with anti-PD-1 (atezolizumab + vemurafenib + cobimetinib; IMspire150) extends PFS over doublet.

Notes

ESCAT IA per ESMO precision-medicine WG. OncoKB Level 1. Companion diagnostics: cobas 4800 BRAF V600 Mutation Test, THxID-BRAF, FoundationOne CDx. V600K behaves clinically like V600E (slightly lower response rates) and shares all approvals.

Used By

No reverse references found in the YAML corpus.