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RET C634R is the most common MEN2A germline variant. In advanced / metastatic MEN2A-drive...

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IDBMA-RET-C634R-MTC
TipoRelevância terapêutica
Estadoreviewed 2026-04-27 | pending_clinical_signoff | actionability review required
DoençasDIS-MTC
FontesSRC-CIVIC SRC-NCCN-CNS-2025

Fatos de ação

BiomarcadorBIO-RET
VarianteC634R (germe — MEN2A)
DoençaDIS-MTC
Nível ESCATIB
Combinações recomendadasselpercatinib em monoterapia, pralsetinib en monoterapia
Contraindicated monotherapycabozantinib/ vandetanib (seletivo-TKI preferido na era seletiva-Tki)
Resumo das provasRET C634R is the most common MEN2A germline variant. In advanced / metastatic MEN2A-driven MTC, selpercatinib and pralsetinib have activity comparable to M918T disease (LIBRETTO-001 RET-mutant MTC cohort). FDA labels for selpercatinib/pralsetinib in RET-mutant MTC encompass germline / extracellular-domain variants. C634R also drives prophylactic-thyroidectomy timing in MEN2A kindred.

Notas

ESCAT IB (slightly lower than M918T because LIBRETTO-531 1L superiority data are most robust in M918T-enriched cohorts; C634 is treated identically by FDA label and clinical practice). OncoKB Level 1. Mandatory pheochromocytoma + hyperparathyroidism screening (MEN2A syndrome). Source-gap: SRC-NCCN-THYROID-2025 placeholder; SRC-LIBRETTO001-DRILON-2020 not yet ingested.

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