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. Author manuscript; available in PMC: 2017 Jul 17.
Published in final edited form as: N Engl J Med. 2016 Sep 8;375(10):944–953. doi: 10.1056/NEJMoa1602074

Table 1.

Demographic and Clinical Characteristics of the Patients.*

Characteristic Cord-Blood Group (N = 140) HLA-Matched Group (N = 344) HLA-Mismatched Group (N = 98)
Age — yr
 Median 29 40 45
 Range 1–64 1–67 2–64
Weight — kg
 Median 70 76 77
 Range 9–112 13–173 12–142
Female sex — no. (%) 68 (49) 150 (44) 45 (46)
Race — no. (%)
 White 64 (46) 294 (85) 76 (78)
 Other 76 (54) 50 (15) 22 (22)
Positive serostatus for cytomegalovirus — no. (%) 86 (61) 178 (52) 47 (48)
Diagnosis — no. (%)
 Acute myeloid leukemia 73 (52) 175 (51) 52 (53)
 Acute lymphoid leukemia 51 (36) 106 (31) 28 (29)
 Myelodysplastic syndrome 16 (11) 63 (18) 18 (18)
Disease risk — no. (%)§
 Low or intermediate 93 (66) 276 (80) 77 (79)
 High or very high 47 (34) 68 (20) 21 (21)
Conditioning regimen — no. (%)
 Fludarabine, cyclophosphamide, and total-body irradiation at a dose of 1320 cGy 97 (69) 0 0
 Treosulfan, fludarabine, and total-body irradiation at a dose of 200 cGy 43 (31) 64 (19) 7 (7)
 Busulfan with either cyclophosphamide or fludarabine 0 127 (37) 54 (55)
 Cyclophosphamide and total body irradiation at a dose of 1200 or 1320 cGy 0 153 (44) 37 (38)
GVHD prophylaxis — no. (%)
 Cyclosporine and mycophenolate mofetil 140 (100)
 Tacrolimus and methotrexate 268 (78) 98 (100)
 Other 76 (22)
Presence of minimal residual disease — no./total no. (%) 45/137 (33) 104/331 (31) 35/90 (39)
*

The chi-square test was used for categorical variables, and analysis of variance for continuous variables. GVHD denotes graft-versus-host disease.

P<0.001 for the difference in the distribution of characteristics among the three groups.

Race was self-reported.

§

Disease risk was categorized as low, intermediate, high, or very high, as previously described.14 P<0.01 for the difference in the distribution of characteristics among the three groups.