Table 1.

Characteristics and response of Philadelphia-positive ALL study groups



No. (%)

Parameter
VAD
Hyper-CVAD
Hyper-CVAD + imatinib mesylate
P
No. treated     
Total   31   50   20   —  
Status at study entry     
Active disease   31   50   15 (75)   —  
In CR   —   —   5 (25)   —  
Age, y [median, range]     
60 or older   8 (26)   15 (30)   4 (20)   NS  
  [47, 19-73]   [44, 16-79]   [42, 19-75]   
Performance, ECOG     
0   7 (23)   3 (6)   4 (20)   .07  
1 to 2   23 (74)   45 (90)   16 (80)   
Hemoglobin, g/L     
Less than 100   14 (45)   35 (70)   13 (65)   .08  
WBC, × 109/L     
30 or higher   15 (48)   22 (44)   4 (20)   NS  
Platelet count, × 109/L     
Lower than 50   15 (48)   29 (58)   7 (35)   NS  
Albumin, g/L     
Lower than 30   4 (13)   7 (14)   7 (35)   .08  
LDH, U/L     
More than 620   30 (97)   46 (92)   12 (60)   < .01  
CNS disease     
Yes   —   1 (2)   3 (15)   .02  
Karyotype     
Ph or complex Ph   12 (39)   17 (34)   8 (40)   NS  
Ph, −5, −7   6 (19)   4 (8)   1 (5)   
Ph and others (+8, +21)   13 (42)   28 (58)   11 (55)   
B2 microglobulin, mg %  13/19   19/39   4/18   .03  
More than 3   (68)   (49)   (22)   
Response     
CR   19 (61)   47 (94)   15/15   < .01  
PR   4 (13)   —   —   
Resistant   8 (26)   3 (6)   —   
CR at start   —   —   5 (25)   
Death   —   —   —   
Courses to CR     
1   16 (84)   33 (70)   14 (93)   NS  
2   3 (16)   6 (13)   1 (7)   
More than 2   —   8 (17)   —   
Median days to response [range]     
CR   24 [19-42]   20 [11-32]   19 [15-22]   NS  
ANC 109/L or higher   22 [6-27]   23 [15-30]   20 [17-28]   
PLT 100 × 109/L or higher   24 [20-48]   25 [18-107]   21 [17-44]   
Incidence during induction*     
FUO   10 (22)   31 (41)   4 (25)   NS  
Infections   8 (17)   27 (36)   5 (31)   
Pneumonia   4   9   3   
Sepsis/bacteremia   2   12   —   
Fungemia   1   1   1   
Other (minor)
 
1
 
5
 
1
 

 


No. (%)

Parameter
VAD
Hyper-CVAD
Hyper-CVAD + imatinib mesylate
P
No. treated     
Total   31   50   20   —  
Status at study entry     
Active disease   31   50   15 (75)   —  
In CR   —   —   5 (25)   —  
Age, y [median, range]     
60 or older   8 (26)   15 (30)   4 (20)   NS  
  [47, 19-73]   [44, 16-79]   [42, 19-75]   
Performance, ECOG     
0   7 (23)   3 (6)   4 (20)   .07  
1 to 2   23 (74)   45 (90)   16 (80)   
Hemoglobin, g/L     
Less than 100   14 (45)   35 (70)   13 (65)   .08  
WBC, × 109/L     
30 or higher   15 (48)   22 (44)   4 (20)   NS  
Platelet count, × 109/L     
Lower than 50   15 (48)   29 (58)   7 (35)   NS  
Albumin, g/L     
Lower than 30   4 (13)   7 (14)   7 (35)   .08  
LDH, U/L     
More than 620   30 (97)   46 (92)   12 (60)   < .01  
CNS disease     
Yes   —   1 (2)   3 (15)   .02  
Karyotype     
Ph or complex Ph   12 (39)   17 (34)   8 (40)   NS  
Ph, −5, −7   6 (19)   4 (8)   1 (5)   
Ph and others (+8, +21)   13 (42)   28 (58)   11 (55)   
B2 microglobulin, mg %  13/19   19/39   4/18   .03  
More than 3   (68)   (49)   (22)   
Response     
CR   19 (61)   47 (94)   15/15   < .01  
PR   4 (13)   —   —   
Resistant   8 (26)   3 (6)   —   
CR at start   —   —   5 (25)   
Death   —   —   —   
Courses to CR     
1   16 (84)   33 (70)   14 (93)   NS  
2   3 (16)   6 (13)   1 (7)   
More than 2   —   8 (17)   —   
Median days to response [range]     
CR   24 [19-42]   20 [11-32]   19 [15-22]   NS  
ANC 109/L or higher   22 [6-27]   23 [15-30]   20 [17-28]   
PLT 100 × 109/L or higher   24 [20-48]   25 [18-107]   21 [17-44]   
Incidence during induction*     
FUO   10 (22)   31 (41)   4 (25)   NS  
Infections   8 (17)   27 (36)   5 (31)   
Pneumonia   4   9   3   
Sepsis/bacteremia   2   12   —   
Fungemia   1   1   1   
Other (minor)
 
1
 
5
 
1
 

 

VAD indicates vincristine, doxorubicin, and dexamethasone; PLT, platelet count; —, not applicable; NS, not significant; and FUO, fever of unknown origin.

*

Only 15 of 20 patients evaluable for induction course toxicity for hyper-CVAD and imatinib mesylate (5 patients in CR at start).

Close Modal

or Create an Account

Close Modal
Close Modal