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. 2021 Sep 7;25(20):9557–9566. doi: 10.1111/jcmm.16895

TABLE 1.

Main clinical and biological characteristics of t(4;12)(q11‐13;p13) cohort

Characteristics n (%)
Total 21
Median age, years (range) 78 (56–92)
Gender, male/female 14 (67)/7 (33)
Median WBC, 109/L (range) 18.2 (0.7–82.9)
Myeloid malignancies
MDS with excess blasts a 2/21 (10)
AML (FAB classification) 19/21 (90)
AML 0 5/19 (26)
AML 1 5/19 (26)
AML 2 5/19 (26)
AML 4 1/19 (5)
Unspecified 3/19 (15)
AML (WHO classification) 19/21 (90)
AML with recurrent genetic abnormalities
AML with mutated NPM1 1/19 (5)
AML with mutated RUNX1 b 2/16 (25)
AML with myelodysplasia‐related changes 12/19 (63)
Therapy‐related AML 1/19 (5)
AML, NOS 3/19 (5)
Cytological characteristics of AML
Multilineage dysplasia 10/19 (53)
Flow cytometry findings of AML blasts
CD33+ 15/15 (100)
CD7+ 11/14 (79)
CD56+ 7/11 (63)
CD7+ and/or CD56 + 13/14 (93)
MPO+ 3/13 (23)
Conventional karyotype
Isolated t(4;12) 10/21 (48)
One additional CA 7/21 (33)
Complex karyotype 4/21 (19)
FISH
ETV6 rearrangement 18/18 (100)
CHIC2 region rearrangement 15/17 (88)

Abbreviations: CA, chromosomal abnormality; MDS, myelodysplastic syndrome; MPN, myeloproliferative neoplasm; NOS, not otherwise specified; WBC, white blood cell count.

a

One MDS with excess blasts (EB)‐1 (7%) and one with EB‐2 (11%).

b

Two other cases with RUNX1 mutations were included in AML with myelodysplasia‐related changes.