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. Author manuscript; available in PMC: 2024 Dec 1.
Published in final edited form as: Am J Hematol. 2023 Sep 9;98(12):1869–1876. doi: 10.1002/ajh.27084

Table 2.

Comparison of patients with newly diagnosed AML who were either recommended for allo-HCT and proceeded to transplant, or recommended for allo-HCT but did not proceed due to persistent disease

Characteristic Overall,
N = 1391
Proceeded to allo-HCT,
N = 105 (76%)1
Persistent disease precluding allo-HCT
N = 34 (24%)1
P value2
Age 61 (51, 67) 59 (49, 65) 63 (56, 71) 0.016
ELN risk stratification 0.13
 Favorable 20 (14%) 16 (15%) 4 (12%)
 Intermediate 41 (29%) 35 (33%) 6 (18%)
 Adverse 78 (56%) 54 (51%) 24 (71%)
Day 14 bone marrow blast % > 0.9
 < 5% 38 (47%) 32 (47%) 6 (46%)
 ≥ 5% 43 (53%) 36 (53%) 7 (54%)
 Not available 58 37 21
AML subtype 0.002
 Therapy-related 19 (14%) 14 (13%) 5 (15%)
 AML – other3 54 (39%) 47 (45%) 7 (21%)
 Secondary AML 10 (7.2%) 3 (2.9%) 7 (21%)
 AML with MDS related changes 56 (40%) 41 (39%) 15 (44%)
1

data summarized as median (IQR) and n (%);

2

Wilcoxon rank sum test; Fisher’s exact test; Pearson’s Chi-squared test;

3

AML – other includes AML with recurrent genetic abnormalities and AML, not otherwise specified. ELN, European Leukemia Net; allo-HCT, allogeneic hematopoietic cell transplantation; MDS, myelodysplasia