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. 2005 Oct 18;107(3):1166–1173. doi: 10.1182/blood-2005-06-2325

Table 1.

Summary of patients' details

Patient ID FAB WBC, × 109 cells/L Karyotype** Risk group
Engrafters
   1* 1 151 Normal Intermediate
   2§ 1 14.7 t(6;9) Intermediate
   3 1 20.3 –5q Poor
   4 1 64 FK Intermediate
   5 1 37 FK Intermediate
   6 1 5.3 Normal Intermediate
   7§ 1 139 +13 Intermediate
   8* 2 104 Normal Intermediate
   9§ 2 66 t(8;21) Good
   10§ 2 27 +11+13 Intermediate
   11 2 39.8 Normal Intermediate
   12 2 29 t(8;9) Intermediate
   13 2 40 t(2;3) Poor
   14 4 2.5 Normal Intermediate
   15 4 71 +3+10 Intermediate
   16 4 8.5 Normal Intermediate
   17 4 221 Normal Intermediate
   18 4 42.9 Normal Intermediate
   19* 5 3.9 Complex Poor
   20 5 115 Normal Intermediate
   21 5 33 Normal Intermediate
   22 5 212 ND Intermediate
   23 5 53.7 t(9;11) Intermediate
   24 5a 42.9 t(11;19) Intermediate
   25 5a 124 +11 Intermediate
   26* tAML 2.7 t(11;19) Intermediate
   27 tAML 25 t(6;11) Intermediate
   28* tAML 19.5 Complex Poor
   29 AML/MDS 31 Inv(3); –7 Poor
Nonengrafters
   30 0 70 –9q +19 Intermediate
   31 1 103 +13 Intermediate
   32# 1 10 –9q Intermediate
   33# 1 86 +8 Intermediate
   34# 1 6.1 Normal Intermediate
   35# 1 1.4 Normal Intermediate
   36§ 1 50 Normal Intermediate
   37 1 248 Normal Intermediate
   38 1 70 t(8;21) Good
   39 2 27.9 t(8;21) Good
   40 2 85 +12+21 Intermediate
   41 2 28 t(8;21) Good
   42 2 11.8 Normal Intermediate
   43 2 71 Normal Intermediate
   44 2 19.2 t(6;9) Intermediate
   45 2 5.7 t(8;21) Good
   46 2 5.5 Normal Intermediate
   47 2 3 Normal Intermediate
   48 3 1 t(15;17) Good
   49 3 1.3 t(15;17) Good
   50# 3 1.9 t(15;17) Good
   51 3 6.1 t(15;17) Good
   52# 3v 35 t(15;17) Good
   53 4 61 Inv 16 Good
   54* 4 85 Normal Intermediate
   55 4 127 Normal Intermediate
   56 4 113 Inv(16) Good
   57 5a 184 ins(10;11) Intermediate
   58# 5a 39 +5; +8; +19 Intermediate
   59 tAML 147 Normal Intermediate

Mice were injected with 107 peripheral blood nucleated cells from the peripheral blood of AML patients. Murine marrows were analyzed 6 weeks after transplantation for the presence of human hematopoietic cells. AML engraftment was defined as the presence of human CD33+/CD45+ myeloid cells without an accompanying CD19+/CD45+ B-cell population. Prognosis risk group was defined as poor, intermediate, or good via karyotype according to Grimwade et al.10 Patients in whom the WBC was less than 2 × 109/L also had their bone marrow cells tested for engraftment capacity, with identical results to the peripheral blood data. All AML cases were assessed for NOD/SCID engraftment potential before any chemotherapy. FK indicates failed karyotype at diagnosis.

*

Patients given supportive care only

Patients possessed an FLT3-ITD

Patients had a mutated nucleophosmin gene

§

Patients in relapse

Patients were tested for FLT3 mutations and were found to be negative

Patients underwent affymetrix analysis

#

Patients produced normal engraftment in NOD/SCID mice

**

Full karyotyping according to the international system for human genotype nomenclature may be found in Table S1