Table 1.

Comparison of clinical leukemia specimens obtained and analyzed

Samples
obtained
Samples analyzed
in present study
AML   
 Number of patients 140  42  
 FAB classification   
  M0   3   1  
  M1  17   9  
  M2  34   10  
  M3  11   1  
  M4  33   7  
  M5  17   8  
  M6  16   4  
  M7   9   2  
 Treatment   
  Timed sequential Ac-D-X* 129  38  
  Individual therapy   8   2  
  No treatment   3   2  
 Age, median (range) 52 (18-79) 56 (18-79)  
 WBC, median (range) 4800 (400-313 000) 9400 (800-258 000)  
 AHD, no. (%) 32 (22%) 8 (19%)  
 Secondary leukemia, no. (%) 16 (11%) 2 (5%)  
 CD34-positive, no. (%) 85/135 (63%) 30/42 (71%)  
 Poor risk karyotype1-153, no. (%) 58/131 (44%) 21/38 (55%)  
 % blasts in analyzed sample, median  67  88  
 CR with first cycle, no. (%)1-155 80/116 (69%) 18/34 (53%)  
ALL   
 Number of patients  29  18  
 T-cell phenotype, no. (%) 10 (34) 5 (28)  
 Age, median (range) 34 (18-74) 29 (18-74)  
 WBC × 10−3, median (range) 26 (0.8-600) 46 (3-312)  
 Ph1chromosome, no. (%) 7/28 (25) 2/17 (12)  
 % blasts, median  85  88  
 CR by day 60, no. (%)1-155 11/21 (52%) 9/12 (75%) 
Samples
obtained
Samples analyzed
in present study
AML   
 Number of patients 140  42  
 FAB classification   
  M0   3   1  
  M1  17   9  
  M2  34   10  
  M3  11   1  
  M4  33   7  
  M5  17   8  
  M6  16   4  
  M7   9   2  
 Treatment   
  Timed sequential Ac-D-X* 129  38  
  Individual therapy   8   2  
  No treatment   3   2  
 Age, median (range) 52 (18-79) 56 (18-79)  
 WBC, median (range) 4800 (400-313 000) 9400 (800-258 000)  
 AHD, no. (%) 32 (22%) 8 (19%)  
 Secondary leukemia, no. (%) 16 (11%) 2 (5%)  
 CD34-positive, no. (%) 85/135 (63%) 30/42 (71%)  
 Poor risk karyotype1-153, no. (%) 58/131 (44%) 21/38 (55%)  
 % blasts in analyzed sample, median  67  88  
 CR with first cycle, no. (%)1-155 80/116 (69%) 18/34 (53%)  
ALL   
 Number of patients  29  18  
 T-cell phenotype, no. (%) 10 (34) 5 (28)  
 Age, median (range) 34 (18-74) 29 (18-74)  
 WBC × 10−3, median (range) 26 (0.8-600) 46 (3-312)  
 Ph1chromosome, no. (%) 7/28 (25) 2/17 (12)  
 % blasts, median  85  88  
 CR by day 60, no. (%)1-155 11/21 (52%) 9/12 (75%) 

AML = acute myelogenous leukemia; ALL = acute lymphocytic leukemia; WBC = white blood cell count; CR = complete response.

*

Includes patients treated with cytarabine, daunorubicin, and amsacrine56 as well as a small number of patients treated with cytarabine, daunorubicin, and etoposide with or without priming doses of GM-CSF56 or interleukin-3.57 In cases where cytokine was administered, samples harvested before cytokine were analyzed.

AHD, antecedent hematologic disorder, ie, myelodysplastic or myeloproliferative syndrome.

Leukemia occurring after prior cytotoxic chemotherapy for a nonhematologic malignancy.

F1-153

Deletions involving chromosomes 5 or 7, trisomy 8, and complex karyotypes.

F1-155

Number of CR ÷ (number of CR + NR).

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