Table 1 Baseline characteristics of KMT2Ar adult AML patients.

From: Rearrangements involving 11q23.3/KMT2A in adult AML: mutational landscape and prognostic implications – a HARMONY study

 

n = 205

Female sex

111 (54.1%)

Median age in years (range)

48.1 (18.6–86.2)

  Age ≥ 60 years

51 (24.9%)

AML type

  De novo AML

148 (72.2%)

  Secondary AML

57 (27.8%)

    AML after MDS

14 (6.8%)

    Therapy-related AML

43 (21%)

Hemoglobin (g/dL)

9.5 [Q1 = 8.3, Q3 = 11.3]

WBC (×109/L)

23.1 [Q1 = 4.7, Q3 = 58]

  (>100 × 109/L)

21 (10.2%)

Platelets (×109/L)

51.5 [Q1 = 29.8, Q3 = 107.5]

Bone marrow % of blasts

83 [Q1 = 70.2, Q3 = 90]

Chromosomal aberrations

  t(9;11)

101 (49%)

  t(11;19)

33 (16%)

  t(6;11)

24 (12%)

  t(10;11)

10 (5%)

  t(11;17)

10 (5%)

  Other KMT2Ar

27 (13%)

Additional chromosomal aberrations

85 (41.6%)

  Complex aberrations (≥2 apart from KMT2Ar)

38 (19%)

  Trisomy 8

37 (18%)

  Derivative 11

12 (6%)

ELN 2022

  Favorable

  Intermediate

101 (49.3%)

  Adverse

104 (50.7%)

Treatment

  Intensive

195 (95%)

  Non-intensive

10 (5%)

Composite complete response

120 (63.8%)

Early death

  30-day mortality

28 (13.6%)

  60-day mortality

36 (17.6%)

Allogeneic HSCT

88 (42.9%)

  In CR1

48 (23.4%)

  In CR2 or later

15 (7.3%)

  Unknown response at allo-HSCT

25 (12.2%)

Median survival in years (95% CI)

1.4 (1.1–1.7)

  1. AML acute myeloid leukemia, MDS myelodysplastic syndrome, WBC white blood cell, ELN European LeukemiaNet, HSCT hematopoietic stem cell transplantation, CR1 first complete remission, CR2 second complete remission, CI confidence interval.