Table 3.

Best responses after first 2 cycles of blinatumomab treatment in patients with high-risk and low-risk genetic abnormalities

n (%)
High-risk genetic abnormalities 
 Constitutional trisomy (n = 4) 
  CR with MRD 4 (100) 
 t(17;19)/TCF3-HLF (n = 2) 
  CR with MRD 2 (100) 
MLL rearrangement (n = 18) 
  CR with MRD 4 (22) 
  CR without MRD 2 (11) 
  PD 7 (39) 
  SD 2 (11) 
  Noncompletion of at least 1 blinatumomab cycle 2 (11) 
  Inevaluable* 1 (6) 
 t(9;22)/BCR-ABL (n = 5) 
  CR with MRD 2 (40) 
  CR without MRD 2 (40) 
  PD 1 (20) 
Low-risk genetic abnormalities 
 t(12;21)/TEL-AML1 (n = 9) 
  CR with MRD 5 (56) 
  CR without MRD 1 (11) 
  Noncompletion of at least 1 blinatumomab cycle 2 (22) 
  PD 1 (11) 
 Hyperdiploidy (n = 6) 
  CR with MRD 2 (33) 
  CR without MRD 2 (33) 
  PD 2 (33) 
n (%)
High-risk genetic abnormalities 
 Constitutional trisomy (n = 4) 
  CR with MRD 4 (100) 
 t(17;19)/TCF3-HLF (n = 2) 
  CR with MRD 2 (100) 
MLL rearrangement (n = 18) 
  CR with MRD 4 (22) 
  CR without MRD 2 (11) 
  PD 7 (39) 
  SD 2 (11) 
  Noncompletion of at least 1 blinatumomab cycle 2 (11) 
  Inevaluable* 1 (6) 
 t(9;22)/BCR-ABL (n = 5) 
  CR with MRD 2 (40) 
  CR without MRD 2 (40) 
  PD 1 (20) 
Low-risk genetic abnormalities 
 t(12;21)/TEL-AML1 (n = 9) 
  CR with MRD 5 (56) 
  CR without MRD 1 (11) 
  Noncompletion of at least 1 blinatumomab cycle 2 (22) 
  PD 1 (11) 
 Hyperdiploidy (n = 6) 
  CR with MRD 2 (33) 
  CR without MRD 2 (33) 
  PD 2 (33) 

PD, progressive disease; SD, stable disease.

*

Bone marrow assessment was not performed because of poor health of the patient after the first blinatumomab cycle.

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