Table 2.

Patient characteristics at study entry


Characteristics

Alternating

Concurrent
Median age, y (range)   46 (21-65)   41 (19-63)  
Sex, no. (%)   
   Male   25 (53)   23 (51)  
   Female   22 (47)   22 (49)  
Subtype of ALL, no. (%)   
   c-ALL   33 (70)   28 (62)  
   Pre-B-ALL   10 (21)   14 (31)  
   NA   0 (0)   3 (7)  
   Lymphoid blast crisis   4 (9)   0 (0)  
BCR-ABL transcripts, no. (%)   
   P210BCR-ABL  20 (43)   12 (27)  
   P190BCR-ABL  26 (55)   31 (69)  
   NA   1 (2)   2 (4)  
Disease status at study start, no. (%)*   
   CR1   44 (94)   24 (54)  
   PR   3 (6)   10 (22)  
   No response   0 (0)   9 (20)  
   NA
 
0 (0)
 
2 (4)
 

Characteristics

Alternating

Concurrent
Median age, y (range)   46 (21-65)   41 (19-63)  
Sex, no. (%)   
   Male   25 (53)   23 (51)  
   Female   22 (47)   22 (49)  
Subtype of ALL, no. (%)   
   c-ALL   33 (70)   28 (62)  
   Pre-B-ALL   10 (21)   14 (31)  
   NA   0 (0)   3 (7)  
   Lymphoid blast crisis   4 (9)   0 (0)  
BCR-ABL transcripts, no. (%)   
   P210BCR-ABL  20 (43)   12 (27)  
   P190BCR-ABL  26 (55)   31 (69)  
   NA   1 (2)   2 (4)  
Disease status at study start, no. (%)*   
   CR1   44 (94)   24 (54)  
   PR   3 (6)   10 (22)  
   No response   0 (0)   9 (20)  
   NA
 
0 (0)
 
2 (4)
 

For patients on the alternating schedule, n = 47; for patients on the concurrent schedule, n = 45.

NA indicates not available; CR1, first complete remission; and PR, partial remission

*

With the alternating schedule, patients were enrolled after INDII if they had achieved a remission in response to induction chemotherapy; with the concurrent administration schedule, patients already entered the study after INDI, irrespective of their response to chemotherapy

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