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letter
. 2017 Nov 27;7(12):633. doi: 10.1038/s41408-017-0004-0

Table 1.

Baseline characteristics of the study population by ASXL1 mutation status (frameshift and nonsense)

MDS cohort CMML cohort
ASXL1 MT ASXL1 WT ASXL1 MT ASXL1 WT
n = 36 n = 159 n = 28 n = 32
Median age (years) 74 (51–92) 72 (34–100) 74 (48–88) 74 (57–94)
Male 25 (69%) 99 (62%) 21 (75%) 20 (63%)
Female 11 (31%) 60 (38%) 7 (25%) 12 (37%)
Median hemoglobin (g/dl) 9.1 9.4 10.1 10.9
Median platelets (G/L) 65 90 92 75
Median ANC 1.32 1.42 7.87 5.67
Median monocyte count 0.22 0.24 1.96 2.58
Median BM Blast % 4 4 4 4
IPSS
  Low 5 (14%) 40 (25%) 12 (43%) 15 (47%)
  Intermediate 1 17 (47%) 50 (31%) 10 (36%) 13 (41%)
  Intermediate 2 3 (8%) 37 (23%) 3 (11%) 4 (12%)
  High 9 (25%) 32 (20%) 3 (11%) 0 (0%)
 # of mutations (median) 2* 1 3 2
ASXL1 Mutationa
  ASXL1 c.1934dupG 7 (19%) 8 (29%)
  Frameshift 25 (69%) 18 (64%)
  Nonsense 11 (31%) 10 (36%)
 HMA treatment 25 (69%) 89 (56%) 16 (57%) 15 (47%)
 Allo-HSCT 7 (19%) 23 (15%) 3 (11%) 4 (13%)
 Median OS (months) 15.5 17.9 11.9** NR

MDS myelodysplastic syndrome, CMML chronic myelomonocytic leukemia, MT mutant, WT, wild type, ANC absolute neutrophil count, BM bone marrow, IPSS international prognostic scoring system, HMA hypomethylating agent, allo-HSCT allogeneic hematopoetic stem cell transplantation, OS overall survival *P < 0.0001; **P = 0.02

a ASXL1 missense mutations occurred in 29% (n = 15) and 7% (n = 2) of the MDS and CMML cohorts, respectively