Table 2.

CR Rates, Survival, and Relapse Risk by Individual Abnormalities

Abnormality Total No.CR and Reason for Failure Deaths in Remission % (SE) Relapse Risk at 5 yr % (SE)Overall Survival at 5 yr % (SE)
CR Rate %Induction Deaths % Resistant Disease %
Overall 1,612  85  8  8  14 (1.1)  49 (1.5)  44 (1.3) 
Favorable  
 t(15;17)  198  87  11  2  13 (3.1) 37 (4.1)* 63 (3.6)* 
 t(8;21)  122  98* 2  0 15 (3.4)  29 (4.5)* 69 (4.2)* 
 inv(16)  57  88  12  0  9 (4.3)  42 (7.4) 61 (6.5) 
Intermediate  
 No abnormality  680  88 6  6  15 (1.7)  53 (2.3)  42 (1.9)  
 +8  148 84  7  8  12 (2.9)  44 (4.8)  48 (4.3) 
 11q23  60  87  7  7  9 (4.6)  47 (7.2) 45 (6.4)  
 +21  45  80  7  13  11 (6.2) 50 (9.0)  47 (7.7)  
 del (7q)  32  75  6  19 19 (10.9)  59 (10.5)  23 (8.1)  
 del (9q)  25 100  0  0  9 (5.8)  39 (10.1)  60 (9.8)  
 +22 22  91  5  5  13 (8.6)  51 (12.4)  59 (10.5) 
 Other numerical  219  76* 11  14* 19 (3.4)  60 (4.2)  29 (3.1)* 
 Other structural 366  76* 9  14* 14 (2.5)  51 (3.2) 35 (2.5) 
Adverse  
 Complex  95  67* 13 20* 12 (4.9)  68 (6.2)* 21 (4.2)* 
 −7 61  54* 16 30* 8 (8.0) 80 (7.1)* 10 (3.8)* 
 abn(3q)  40  63* 23 15  20 (11.9)  85 (7.8)* 12 (6.2)* 
 del(5q)  28  57* 14  29* 14 (9.1) 85 (9.5)* 11 (5.8)* 
 −5  26  42* 12 46* 12 (11.7)  90 (9.8) 4 (3.8)* 
Abnormality Total No.CR and Reason for Failure Deaths in Remission % (SE) Relapse Risk at 5 yr % (SE)Overall Survival at 5 yr % (SE)
CR Rate %Induction Deaths % Resistant Disease %
Overall 1,612  85  8  8  14 (1.1)  49 (1.5)  44 (1.3) 
Favorable  
 t(15;17)  198  87  11  2  13 (3.1) 37 (4.1)* 63 (3.6)* 
 t(8;21)  122  98* 2  0 15 (3.4)  29 (4.5)* 69 (4.2)* 
 inv(16)  57  88  12  0  9 (4.3)  42 (7.4) 61 (6.5) 
Intermediate  
 No abnormality  680  88 6  6  15 (1.7)  53 (2.3)  42 (1.9)  
 +8  148 84  7  8  12 (2.9)  44 (4.8)  48 (4.3) 
 11q23  60  87  7  7  9 (4.6)  47 (7.2) 45 (6.4)  
 +21  45  80  7  13  11 (6.2) 50 (9.0)  47 (7.7)  
 del (7q)  32  75  6  19 19 (10.9)  59 (10.5)  23 (8.1)  
 del (9q)  25 100  0  0  9 (5.8)  39 (10.1)  60 (9.8)  
 +22 22  91  5  5  13 (8.6)  51 (12.4)  59 (10.5) 
 Other numerical  219  76* 11  14* 19 (3.4)  60 (4.2)  29 (3.1)* 
 Other structural 366  76* 9  14* 14 (2.5)  51 (3.2) 35 (2.5) 
Adverse  
 Complex  95  67* 13 20* 12 (4.9)  68 (6.2)* 21 (4.2)* 
 −7 61  54* 16 30* 8 (8.0) 80 (7.1)* 10 (3.8)* 
 abn(3q)  40  63* 23 15  20 (11.9)  85 (7.8)* 12 (6.2)* 
 del(5q)  28  57* 14  29* 14 (9.1) 85 (9.5)* 11 (5.8)* 
 −5  26  42* 12 46* 12 (11.7)  90 (9.8) 4 (3.8)* 

The prognostic significance of specific cytogenetic abnormalities is considered, irrespective of the presence of additional/secondary cytogenetic changes. On the basis of response to therapy, relapse risk, and overall survival, three prognostic groups were defined.

*

P < .001: P values are for Fisher exact test (CR and reasons for failure) or log rank test (deaths in remission, relapse risk, and overall survival) comparing each abnormality with normal karyotype (ie, no abnormality). All P values remain significant when stratified by age, type of leukemia (de novo or secondary) and WBC at presentation, except for inv(16) where the P value for survival becomes P = .1 when stratified by age. Percentages may not add to 100 because of rounding.

P < .01.

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