Table 1.

Patient characteristics

CharacteristicNo. (%)
Total patients 150 (100) 
Male sex 80 (53) 
Male donor 96 (64) 
Median age (IQR), y 57 (50-65) 
Median donor age (IQR), y 28 (22-40) 
Donor  
 Related 33 (22) 
 Unrelated 117 (78) 
Graft source  
 Peripheral blood stem cell 131 (87) 
 Bone marrow 19 (13) 
HLA match  
 MRD 10/10 allele matched 30 (20) 
 MUD 10/10 + 9/10 allele matched 98 (65) 
 MUD 1 antigen mismatch 19 (13) 
 Haploidentical 3 (2) 
Underlying disease*  
 Acute leukemia 58 (39) 
 Other 92 (61) 
Disease risk  
 High 51 (34) 
 Low 99 (66) 
Karnofsky score at aHSCT  
 <90 25 (17) 
 90-<100 72 (48) 
 100 51 (34) 
 NA 2 (1) 
Conditioning regimen  
 Myeloablative 62 (41) 
 Nonmyeloablative 88 (59) 
Radiation  
 None 38 (25) 
 ≤400 Gy 88 (59) 
 ≥1200 Gy 24 (16) 
T-cell depletion  
 Yes 17 (11) 
 No 133 (89) 
CharacteristicNo. (%)
Total patients 150 (100) 
Male sex 80 (53) 
Male donor 96 (64) 
Median age (IQR), y 57 (50-65) 
Median donor age (IQR), y 28 (22-40) 
Donor  
 Related 33 (22) 
 Unrelated 117 (78) 
Graft source  
 Peripheral blood stem cell 131 (87) 
 Bone marrow 19 (13) 
HLA match  
 MRD 10/10 allele matched 30 (20) 
 MUD 10/10 + 9/10 allele matched 98 (65) 
 MUD 1 antigen mismatch 19 (13) 
 Haploidentical 3 (2) 
Underlying disease*  
 Acute leukemia 58 (39) 
 Other 92 (61) 
Disease risk  
 High 51 (34) 
 Low 99 (66) 
Karnofsky score at aHSCT  
 <90 25 (17) 
 90-<100 72 (48) 
 100 51 (34) 
 NA 2 (1) 
Conditioning regimen  
 Myeloablative 62 (41) 
 Nonmyeloablative 88 (59) 
Radiation  
 None 38 (25) 
 ≤400 Gy 88 (59) 
 ≥1200 Gy 24 (16) 
T-cell depletion  
 Yes 17 (11) 
 No 133 (89) 

All data are no. (%) unless otherwise stated.

IQR, interquartile range; MRD, matched related donor; MUD, matched unrelated donor; NA, not available.

*

Underlying diseases include acute lymphoblastic leukemia (ALL), acute myeloblastic leukemia, acute nonlymphocytic leukemia, acute myelomonocytic leukemia, acute monocytic leukemia, and chronic ALL.

Factors for high risk of disease include greater than first complete remission or primary induction failure for acute leukemia, non-Hodgkin leukemia, Hodgkin l, chronic lymphocytic leukemia, myelodysplastic syndrome (MDS) with refractory anemia and excess blasts, prolymphocytic leukemia (PLL), and severe aplastic anemia. Factors for low risk of disease include first complete remission of acute leukemia; biphenotypic, bilineage, or hybrid leukemia; chronic myeloblastic leukemia; Diamond-Blackfan anemia; MDS (minus refractory anemia with excess blasts); precursor T-cell lymphoblastic lymphoma; peripheral T-cell lymphoma; splenic marginal zone B-cell lymphoma; PLL T-cell lymphoma, and PLL B-cell lymphoma.

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