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PIK3CA hotspot mutation

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

IDBIO-PIK3CA-MUTATION
TypeBiomarker
Aliases
Гарячі мутації PIK3CA
Statuspending_clinical_signoff
DiseasesNone declared
SourcesNone declared

Biomarker Facts

Biomarker typegene_mutation
Mutation details{"functional_impact": "PI3K-alpha pathway activation", "gene": "PIK3CA", "hotspots": ["E542K", "E545K", "H1047R", "H1047L"], "type": "activating missense"}
Measurement
MethodTumor-tissue NGS panel OR plasma ctDNA NGS — both ASCO/CAP-acceptable
Sensitivity requirementVAF detection threshold ≥1% recommended for ctDNA
Related biomarkersNone declared

Notes

Companion diagnostic for alpelisib. Tissue + ctDNA both acceptable; ctDNA preferred when fresh tissue unavailable. UA-availability of alpelisib gates the clinical actionability.

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