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IDH1 mutation in B-ALL is rare. Tissue-agnostic ivosidenib not approved in lymphoid; per...

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

IDBMA-IDH1-R132H-B-ALL
TypeActionability
Statusreviewed 2026-04-27 | pending_clinical_signoff | actionability review required
DiseasesDIS-B-ALL
SourcesSRC-CALGB-10403-STOCK-2019 SRC-CIVIC

Actionability Facts

BiomarkerBIO-IDH-MUTATION
VariantIDH1 R132H
DiseaseDIS-B-ALL
ESCAT tierIV
Evidence summaryIDH1 mutation in B-ALL is rare. Tissue-agnostic ivosidenib not approved in lymphoid; per usual B-ALL pediatric/adult protocol.

Notes

ESCAT IV.

Used By

No reverse references found in the YAML corpus.