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. Author manuscript; available in PMC: 2023 Jan 3.
Published in final edited form as: Biol Blood Marrow Transplant. 2017 Mar 15;23(7):1064–1071. doi: 10.1016/j.bbmt.2017.03.017

Table 1:

Characteristics of all patients included in the analysis

Characteristic N (%)
N 104
Men (%) 51 (49%)
Median age at transplant, years (range) 58 (21–78)
Number of patients with molecular and flow analysis
 Molecular analysis at diagnosis 58 (55.8)
 Molecular analysis pre-HCT 83 (79.8)
 Paired molecular analysis at diagnosis and pre-HCT 47 (45.2)
 Flow MRD analysis pre-HCT 77 (74.0)
 Paired flow and molecular analysis pre-HCT 62 (59.6)
AML characteristics
Primary AML 65 (62.5)
Secondary AML, prior disease 39 (37.5)
 Prior MDS 21
 Prior MPN 7
 Prior CMML 0
 Therapy related AML ^ 15
CIBMTR Cytogenetics Grouping
 Favorable 2 (1.9)
 Intermediate 88 (84.6)
 Adverse 14 (13.5)
Remission status at time of HCT
 CR1 59 (56.7)
 CR2 9 (8.7)
 CR3 1 (1.0)
 CRi 21 (20.2)
 Not in CR 14 (13.5)
DRI
 Low 2 (1.9)
 Intermediate 71 (68.3)
 High 30 (28.8)
 Very high 1 (1.0)
HCT-CI
 <3 51 (49)
 ≥3 53 (51)
Stem cell source
 Peripheral blood stem cells 73 (70.2)
 Bone marrow derived stem cells 12 (11.5)
 Cord blood 19 (18.3)
CD34+ selection 29 (27.9)
HLA match #
 Fully matched 72 (69.2)
 Mismatched 32 (30.8)
Conditioning intensity
 Ablative 59 (56.7)
 Reduced intensity 45 (43.3)
Transplant
 First 95 (91.3)
 Second 9 (8.7)
Outcomes
 Relapse, N (%) 22 (21.2)
 Deceased, N (%) 36 (34.6)
Cause of death
 Relapse 13 (12.5)
 Infection 10 (9.6)
 GVHD 6 (5.8)
 Toxicity 2 (1.9)
 Organ failure 4 (3.8)
 Unknown 1 (0.8)
^

2 patients developed therapy related AML after initial diagnosis with therapy related MDS

*

15 patients did not have available FLT3 mutation testing in the setting of a normal karyotype and thus could not be categorized by the NCCN AML classification.

#

Number of mismatches at high resolution at HLA class 1 (A, B, C) and class 2 (DR and DQ). All cord blood transplants were mismatched.