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. 2014 May 13;124(1):96–105. doi: 10.1182/blood-2014-01-549352

Table 1.

Characteristics of the 22 pre-B ALL patients/leukemia samples investigated in engraftment studies

UPN Age (years) Gender Disease status Sample type Cytogenetics Major cytogenetic group/risk status
1 59.4 F Diagnosis PB Failed* t(9;22)/high
2 44.5 F Diagnosis PB 45,XX,-7,t(9;22)(q34;q11)[4] t(9;22)/high
3 19.5 M Diagnosis BM Normal Normal/standard
4 26.1 M Diagnosis BM 55-56, XY,+X,+4,+6,+11,+12,+14,+17,+18,+21,+21[cp4]/46,XY[4] High hyperdiploidy/
standard
5 46.4 F Diagnosis BM 46,XX,t(9;22)(q34;q11)[1]/46,idem,der(10)t(10;20)(q22;p12)?del(10)(q22q34),der(20)t(10;20)[7]/46,XX[3] t(9;22)/high
6 33.6 M Diagnosis PB 46,XY,+1,dic(1;9)(p1;p1)[8]/46,XY[2] Other/standard
7 42.6 M Diagnosis PB 46,XY,t(4;11)(q21;q23)[10] t(4;11)/high
8 39.7 M Diagnosis BM 46,XY,der(9)add(9)(p11)add(9)(q34)[16]/46,XY[4] Other/standard
9 47.7 M Diagnosis BM 46,XY[20] Normal/standard
10 42.8 F Diagnosis PB 46,XX,t(2;11)(p11;p11),t(4;11)(q21;q23),i(7)(q10),add(22)(q13)[18]/46,XX[2] t(4;11)/high
11 39.8 M Diagnosis PB 59-62,XXYY,-1,-2,-3,-7,+8,add(9)(p1),der(9)t(9;22)(q34;q11)x2,-10,-12,-14,-15,-19,-20,+21,-22,-22,+2mar[cp6] t(9;22)/high
12 22.7 M Diagnosis BM 47,XY,+21c[20] t(12;21)/standard
13 50.4 M Diagnosis BM 46,XY,t(9;22)(q34;q11)[3]/46,XY[1] t(9;22)/high
14 48.2 M Diagnosis PB 46,XY,t(4;11)(q21;q23)[19]/46,XY[1] t(4;11)/high
15 49.3 F Diagnosis PB 46,XX,del(5)(q11q1?3),add(9)(p2?4)x2,der(19)t(1;19)(q23;p13)[35]/46,XX[5] t(1;19)/standard
16 42.7 M Diagnosis PB 46,XY,der(15)t(1;15)(q2;p1),der(19)t(1;19)(q23;p13)[11] t(1;19)/standard
17 50.2 F Diagnosis BM Normal Normal/standard
18 52.4 M Diagnosis BM 45∼46,XX,inv(1)(p2q2),-4,add(4)(q2),del(6)(q1q2),add(8)(q24),add(9)(p2),add(9)(q2),-11,+2mar[cp10] Complex/high
19 48.7 M Diagnosis BM 46,XX,t(9;22)(q34;q11.2)[16]/46,XX[4]. t(9;22)/high
20 32.0 M Diagnosis PB 45,XY,der(1)inv(1)(p3q4)t(1;5)(?;q?),der(5)t(1;5),-7,t(9;22)(q34;q11)[10] t(9;22)/high
21 68.0 F 1st Relapse BM Failed NA
22 27.0 M Diagnosis BM 46,XY,t(4;11)(q21;q23)[6]/46,XY[1] t(4;11)/high

Cytogenetic profiles were determined by local laboratories using standard methods. NA, not applicable; UPN, unique patient number.

*

FISH positive for BCR/ABL gene rearrangement.

FISH positive for TCF3(E2A)-PBX1 gene fusion.

This case had low hypodiploidy (30-39 chromosomes) at diagnosis. FISH analysis at relapse detected loss of the ABL1 and BCR signals consistent with the low hypodiploid clone seen at diagnosis.