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. 2017 Aug 8;117(6):801–812. doi: 10.1038/bjc.2017.256

Table 1. Clinicopathological features of the childhood ALL patients.

Variables N (%)
Gender  
 Male 73 (58.4)
 Female 52 (41.6%)
Age  
 1–9 years 84 (67.2)
 <1 or ⩾10 years 41 (32.8)
WBC  
 <50 000 cells per μl 102 (81.6)
 ⩾50 000 cells per μl 23 (18.4)
Immunophenotype  
 Precursor B-ALL 110 (88.0)
  CD10+ 104 (83.2)
  CD10− 6 (4.8)
 T-ALL 15 (12.0)
High hyperdiploidy (>50 chromosomes)  
 Yes 22 (17.6)
 No 102 (81.6)
 Unknown 1 (0.8)
Hypodiploidy (⩽45 chomosomes)  
 Yes 4 (3.2)
 No 120 (96.0)
 Unknown 1 (0.8)
TEL-AML1/t(12;21)(p13;q22)  
 Negative 93 (74.4)
 Positive 31 (24.8)
 Unknown 1 (0.8)
Philadelphia chromosome BCR-ABL1/t(9;22)(q34;q11)  
 Negative 122 (97.6)
 Positive 2 (1.6)
 Unknown 1 (0.8)
BM on day 15  
 M1 (blasts <5%) 103 (82.4)
 M2 (blasts 5–25%) 16 (12.8)
 M3 (blasts >25%) 6 (4.8)
MRD on day 15  
 <0.01% 22 (17.6)
 >0.01% 67 (53.6)
 Unknown 36 (28.8)
MRD on day 33  
 <0.01% 50 (40.0)
 >0.01% 21 (16.8)
 Unknown 54 (43.2)
Prednisone response on day 8  
 Good (<1000 blasts) 112 (89.6)
 Poor (⩾1000 blasts) 13 (10.4)
BFM risk groups  
 Standard risk 16 (12.8)
 Intermediate risk 87 (69.6)
 High risk 22 (17.6)
Treatment outcome  
 Disease relapse  
 CCR 106 (84.8)
 Relapse 19 (15.2)
Patients’ survival  
 Alive 102 (81.6)
 Dead 23 (18.4)

Abbreviations: ALL=acute lymphoblastic leukaemia; B-ALL=B-lineage acute lymphoblastic leukaemia; BFM=Berlin–Frankfurt–Münster; BM=bone marrow; CCR=complete continuous remission; CD10=cluster of differentiation 10 (common acute lymphoblastic leukaemia antigen, CALLA); MRD=minimal residual disease; T-ALL=T-lineage acute lymphoblastic leukaemia; TEL-AML1=TEL-AML1 rearrangement; WBC=white blood cell.