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Table 1 Clinical and laboratory characteristics of distinct cytogenetic subgroups of the studied patients with B-ALL (n = 71)

From: BCR::ABL1-like acute lymphoblastic leukaemia: a single institution experience on identification of potentially therapeutic targetable cases

Parameter

BCR::ABL1-like n = 6

Ph-negative other n = 33

Ph-negative KMT2A-r

n = 7

Ph-negative

TCF3::PBX1-positive n = 3

BCR::ABL1-positive

n = 22

Male; n (%)

5 (83.3%)

25 (75.6%)

0

1 (33.3%)

8 (36.4%)

Age (years)

 Median (range)

31.5 (21–55)

32 (18–69)

35 (29–59)

49 (24–55)

43 (19–68)

Immunophenotype

 B-common

5

23

0

1

21

 Pro-B

1

8

6

0

1

 Pre-B

0

2

0

1

0

 NOS

0

0

1

1

0

Aberrant expression of myeloid antigens

     

 n (%)

4 (66.7%)

10 (30.3%)

0

0

13 (59.1%)

WBC (× 109/L)

     

Median (range)

38.2 (9.4–220)

4.7 (0.5–208)

44.5 (4.8–259.5)

3.35 (2.6–34)

11.5 (0.9–131.1)

CNSi; n (%)

1 (9.1%)

4 (12.1%)

4 (57.1%)

1 (33.3%)

6 (27.3%)

Response to induction

 CR MRD; n (%)

4 (66.7%)

18 (54.5%)

7 (100%)

1 (33.3%)

12 (54.5%)

 CR MRD+; n (%)

2 (33.3%)

4 (12.1%)

0

2 (66.7%)

8 (36.4%)

AlloHSCT; n (%)

3 (50%)

16 (48.5%)

4 (57.1%)

2 (66.7%)

14 (63.65%)

Alive; n (%)

2 (33.3%)

15 (45.5%)

2 (29%)

1 (33.3%)

15 (68.2%)

  1. B-ALL B cells acute lymphoblastic leukemia, NOS not otherwise specified, WBC white blood cells, CNSi central nervous system involvement, Myeloid antigens CD13, CD33, CD36, CD117, CR complete remission, MRD minimal residual disease, alloHSCT allogeneic stem cells transplantation; complex karyotype: ≥ 3 unrelated (acquired) chromosomal abnormalities; another result: abnormal but non-complex karyotype