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Updated: Jan 30, 2026

Author Spotlight: Advancing the Detection of Low-Frequency Mutations in Cancer Tissues
Published on: August 23, 2024
Myeloid malignancies with somatic GATA2 mutations can be associated with an immunodeficiency phenotype
Mansour Alfayez1, Sa A Wang2, Sarah A Bannon3
1a Department of Leukemia , The University of Texas MD Anderson Cancer Center , Houston , TX , USA.
Abstract:
Germline mutations in GATA2 are associated with a complex immunodeficiency and cancer predisposition syndrome. Somatic GATA2 in myeloid malignancies may impart a similar phenotype. We reviewed adult patients with a diagnosis of GATA2 hematological malignancy who were referred to our HHMC for genetic testing, and identified to have somatic GATA2. Nine patients with a median age of 63 years were included. Six patients (66.7%) were males. Atypical CML and acute myeloid leukemia were the most common initial presentation. The median overall VAF was 47.14%. Monocytopenia was pronounced when the GATA2 involved the C-terminal ZFD. GATA2 N-terminal ZFD mutations tend to be co-mutated with biCEBPA. Unlike germline GATA2 mutations, monocytopenia associated with somatic GATA2 mutations often resolved at remission. We concluded that similar to germline GATA2 mutations, a subset of somatic GATA2 mutations can impart a germline phenotype.
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