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KMT2A-Umlagerung (MLL-Fusion)

Deterministische Ansicht der Quelle YAML Entität. Klinische Autorität bleibt mit den zitierten Quell-IDs und Rezensenten Sign-off Zustand.

IDBIO-KMT2A-REARRANGEMENT
ArtBiomarker
Aliase
11q23 NeuordnungKMT2A-UmstellungKMT2A-rFusion MLLMLL-UmstellungПеребудова KMT2A (фузія MLL)
Statusreviewed 2026-04-30 | pending_clinical_signoff
ErkrankungenDIS-AML DIS-B-ALL
QuellenSRC-ELN-AML-2022 SRC-NCCN-AML-2025

Biomarker-Fakten

Biomarker-Typgene_fusion
Angaben zur Mutation{"functional_impact": "Aberrant transcriptional activation of HOX-A cluster (HOXA9 / MEIS1) via menin-MLL complex; leukemogenic", "gene": "KMT2A", "partners": ["MLLT3 (AF9, t(9;11))", "MLLT1 (ENL, t(11;19))", "AFDN (AF6, t(6;11))", "ELL, t(11;19)", "AFF1 (AF4, t(4;11))", "MLLT10 (AF10)"], "variant_type": "chromosomal rearrangement (typically 11q23 translocation)"}
Messung
VerfahrenKaryotyp + FISH (KMT2A Break-Apart-Sonde) bei Diagnose; RT-PCR / RNA-NGS zur Fusions-Partner-Identifikation
Einheitencategorical (positive | negative); fusion partner reported when known
Verwandte BiomarkerBIO-NPM1

Anmerkungen

KMT2A rearrangements occur in ~5-10% of adult AML and ~70% of infant ALL/AML; ELN-2022 classifies as adverse risk in AML. Mechanism: KMT2A fusion proteins recruit menin to drive HOXA / MEIS1 expression — menin-MLL interaction is the therapeutic target. Revumenib (menin inhibitor; AUGMENT-101 phase 1/2) FDA-approved Nov 2024 for relapsed/ refractory KMT2A-rearranged acute leukemia (≥1 prior line). ORR ~63% with CR/CRh ~23% in KMT2A-r AML. Differentiation syndrome (~16%) and QTc prolongation are signature AEs. Ziftomenib is alternative menin inhibitor in late-phase trials. Common partners: AF9 (t(9;11)) and AF4 (t(4;11)) — diagnostic karyotype + FISH break-apart probe is standard; fusion partner identification by RT-PCR or RNA-NGS informs prognosis (some partners higher risk than others).

Verwendet von

Therapeutische Relevanz