Skip to main content
. 2011 Feb 4;117(16):4262–4272. doi: 10.1182/blood-2010-07-299248

Table 1.

Study subject characteristics

Patient/donor Age, y Sex Source; % blasts Disease* Status Cytogenetics
AML1 79 M LP; 87% AML-M1 Untreated +8
AML2 61 M PB; 66% AML-M2 Relapse +14; FLT3+ (ITD)
AML3 73 F PB; 64% AML-M5 Refractory −5,−12
AML4 53 M LP; 96% AML-M5 Untreated +8; t(9;11)
AML5 24 M LP; 85% AML-M1 Untreated FLT3+ (ITD)
AML6A2− 41 F PB; 98% AML-M1 Untreated Diploid
AML7 38 M PB; 65% AML-M7 Refractory −1,−5,−7,−9,−21
AML8 81 F PB; 92% AML-M1 Untreated Diploid
AML9 64 F PB; 70% AML-M1 Untreated Diploid
ALL1 65 F BM; 78% B-ALL Untreated −2,−3,−4,−7,−9
ND1 34 M PB NA NA NA
ND2 42 F PB NA NA NA
ND3 35 F PB NA NA NA
ND4 38 M PB NA NA NA
ND5 32 M BM NA NA NA
ND6 53 M BM NA NA NA
ND7 26 M BM NA NA NA
ND8 30 M BM NA NA NA
ND9 58 F BM NA NA NA
ND10 31 M BM NA NA NA

A2− superscript indicates HLA-A2–negative; LP, leukapheresis collection; PB, peripheral blood; BM, bone marrow; ND, normal donor; and NA, not applicable.

*

FAB subtype.

Antecedent myelodysplastic syndrome.

Ph-chromosome–negative.