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. 2010 Feb 2;115(16):3224–3230. doi: 10.1182/blood-2009-11-251595

Table 1.

Patient and graft characteristics

Demographics Related (n = 78) Unrelated (n = 39) Total (n = 117)
Median age, y (range) 48 (21-66) 52 (22-66) 50 (21-66)
Female sex, no. (%) 35 (45) 23 (59) 58 (50)
Disease, no.
    De novo AML* 20 13 33
        CR1*/CR ≥ 2 5/4 5/4 10/8
        Not in CR 11 4 15
    Secondary AML 16 9 25
        CR1*/CR ≥ 2 8/1 7/1 15/2
        Not in CR 7 1 8
    MDS 6 8 14
        Secondary 3 3 6
        Not in CR 5 8 13
    ALL 7 3 10
        Not in CR 1 0 1
    CML 3 5 8
        Accelerated phase/active disease 1 1 2
        Chronic phase/active disease 1 4 5
        Chronic phase in CR2 1 0 1
    CLL, all refractory 2 1 3
    Multiple myeloma 5 0 5
        Not in CR 4 0 4
    NHL 8 0 8
        Not in CR 6 0 6
    Hodgkin lymphoma 11 0 11
        Not in CR 11 0 11
Cytomegalovirus serology
    CMV DR 27 12 39
    CMV D+R 15 5 20
    CMV D+R+ 16 5 21
    CMV DR+ 18 17 35
Donor/recipient sex, no.
    Female → male 21 4 25
    Other 57 34 91
Infused cell doses, median (IQR)
    Total nucleated cells, × 108/kg 4.1 (3.4-4.8) 4.0 (3.0-4.7) 4.1 (3.2-4.7)
    CD34+ cells, × 106/kg 3.6 (2.8-4.8) 3.9 (2.8-5.5) 3.7 (2.8-4.9)

IQR indicates interquartile range.

*

A total of 10 patients with de novo AML were in CR1 (5 unrelated, 5 related) with following high-risk disease: Flt-3+ mutation (4), monosomy 7 (1), more than 3 cytogenetic abnormalities (1), t(11;19) (1), t(9;11) plus trisomy 8 and leukemia cutis (1), primary refractory but with CR following reinduction (1), and morphologic CR with aberrant blast phenotype by flow cytometry (1).

A total of 7 patients with ALL who underwent transplantation in CR1 had high-risk disease: Ph+ ALL (4), t(4;11) (1), natural killer ALL (1), T-cell lymphoblastic lymphoma (1).

Data are available for 115 donor/recipient pairs.