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RET M918T mutation (MEN2B / sporadic MTC)

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

IDBIO-RET-M918T
TypeBiomarker
Aliases
RET M918TМутація RET M918T (MEN2B / спорадичний МРЩЗ)
Statusreviewed 2026-04-27 | pending_clinical_signoff
DiseasesNone declared
SourcesSRC-NCCN-THYROID-2025

Biomarker Facts

Biomarker typegene_mutation
Mutation details{"exon": "16", "functional_impact": "activating; intracellular kinase domain — constitutive RET dimerization-independent activation", "gene": "RET", "hgvs_protein": "p.M918T", "variant_type": "missense"}
Measurement
MethodGermline NGS (MEN2 panel) for hereditary screening; tumor NGS for sporadic MTC
Unitscategorical (positive | negative)
Actionability lookup{"gene": "RET", "variant": "M918T"}
Related biomarkersBIO-RET

Notes

Most aggressive RET mutation. Germline → MEN2B (multiple endocrine neoplasia type 2B) — defines need for prophylactic thyroidectomy before age 1. Sporadic in ~25% of MTC, associated with poorer prognosis. Selpercatinib (Retsevmo) and pralsetinib (Gavreto) — selective RET inhibitors; LIBRETTO-001 ORR ~60-70% in advanced MTC. Replaced multikinase inhibitors (vandetanib, cabozantinib) as 1L systemic therapy in actionable RET-altered advanced MTC.

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