Table 1.

Clinical characteristics and outcome of patients included in the GMALL MRD trials


Variable

GMALL 05/93 MRD pilot trial

GMALL 06/99
Total no. patients   65   196  
Sex, no. (%)   
   Male   43 (66)   125 (64)  
   Female   22 (34)   71 (36)  
Median age, y (range)   35 (16-66)   30 (15-64)  
No. patients (%)   
   Younger than 35 y   32 (49)   121 (62)  
   35 y and older   33 (51)   75 (38)  
Median WBC count, × 109/L, (range)*  17.6 (1.7-338)   8.9 (0.86-731.1)  
No. patients with WBC count (%)   
   Less than 30 × 109/L   36 (60)   153 (81)  
   30 × 109/L or more   24 (40)   36 (19) 
Immunophenotype, no. (%)   
   B-lineage   52 (80)   124 (63)  
   T-lineage   13 (20)   72 (37)  
Presence of adverse prognostic factors, no. (%)
 
27 (42)
 
0 (0)§
 

Variable

GMALL 05/93 MRD pilot trial

GMALL 06/99
Total no. patients   65   196  
Sex, no. (%)   
   Male   43 (66)   125 (64)  
   Female   22 (34)   71 (36)  
Median age, y (range)   35 (16-66)   30 (15-64)  
No. patients (%)   
   Younger than 35 y   32 (49)   121 (62)  
   35 y and older   33 (51)   75 (38)  
Median WBC count, × 109/L, (range)*  17.6 (1.7-338)   8.9 (0.86-731.1)  
No. patients with WBC count (%)   
   Less than 30 × 109/L   36 (60)   153 (81)  
   30 × 109/L or more   24 (40)   36 (19) 
Immunophenotype, no. (%)   
   B-lineage   52 (80)   124 (63)  
   T-lineage   13 (20)   72 (37)  
Presence of adverse prognostic factors, no. (%)
 
27 (42)
 
0 (0)§
 
*

Exact white-blood cell (WBC) count was available for 60 of 65 GMALL 05/93 patients and 189 of 196 GMALL 06/99 patients

All patients with a WBC count greater than 30 × 109/L had a T-lineage ALL, as in B-lineage ALL a WBC count greater than 30 × 109/L was defined as adverse prognostic factor

Adverse prognostic factors were: subtype of a pro-B-ALL (n = 6), presence of a t(9;22)/BCR-ABL (n = 14) or a t(4;11)/MLL-AF4 (n = 2) (cytogenetic/molecular data available for 45 patients), WBC count greater than 30 × 109/L in B-lineage ALL (n = 12)

§

Absence of adverse prognostic factors was the precondition for inclusion into GMALL 06/99 MRD SR trial

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