Table 2.

Characteristics of 25 patients who received blinatumomab mAb1 and inotuzumab mAb2 stratified according to the receipt of other interim therapy between mAb1 and mAb2

CharacteristicAll (N = 25)No interim therapy (n = 12)Received interim therapy (n = 13)P
Median age at diagnosis (IQR, y) 43.6 (24.4-60.7) 42.0 (21.2-65.0) 43.6 (32.4-47.6) .46 
Age >45 y 12 (48.0%) 6 (50.0%) 6 (46.2%) .84 
Male sex 13 (52.0%) 5 (41.7%) 8 (61.5%) .32 
Median number of prior lines of therapy before blinatumomab (range, lines) 1 (1-5) 2 (1-3) 1 (1-5) .04 
Prior alloHSCT before mAb1 3 (12.0%) 1 (8.3%) 2 (15.4%) 1.00 
High-risk cytogenetic abnormalities 10 (40.0%) 4 (33.3%) 6 (46.2%) .21 
Philadelphia chromosome positive 4 (16.0%) 3 (25.0%) 1 (7.1%) .32 
Presence of MLL rearrangement 1 (4.0%) 1 (8.3%) 0 (0.0%) 1.00 
Disease burden at the time of blinatumomab mAb1    .59 
 MRD 7 (28.0%) 4 (33.3%) 3 (23.1%)  
 Morphologic disease 18 (72.0%) 8 (66.7%) 10 (76.9%)  
Site of disease at the time of blinatumomab mAb1    .78 
 Isolated marrow 21 (84.0%) 10 (83.3%) 11 (84.6%)  
 Isolated extramedullary 1 (4.0%) 0 (0.0%) 1 (7.7%)  
 Both 3 (12.0%) 2 (16.7%) 1 (7.7%)  
Median no. of blinatumomab mAb1 cycles (range, cycles) 1 (1-6) 1 (1-6) 1 (1-4) .53 
Best response to blinatumomab mAb1    .32 
 CR 13 (52.0%) 5 (41.7%) 8 (61.5%)  
 No response 12 (48.0%) 7 (58.3%) 5 (38.5%)  
Median time from blinatumomab to progression/relapse (IQR, d) 73 (34-219) 65 (37-118) 73 (33-290) .85 
Site of disease at the time of relapse following blinatumomab mAb1    .41 
 Isolated marrow 15 (60.0%) 8 (66.7%) 7 (53.8%)  
 Isolated extramedullary 1 (4.0%) 1 (8.3%) 0 (0.0%)  
 Both 9 (36.0%) 3 (25.0%) 6 (46.2%)  
Central nervous system involvement at the time of relapse after blinatumomab mAb1 1 (4.0%) 0 (0.0%) 1 (7.7%) .48 
Response to inotuzumab mAb2    .89 
 CR 17 (68.0%) 8 (69.2%) 9 (69.2%)  
 No response 8 (32.0%) 4 (30.8%) 4 (30.8%)  
CharacteristicAll (N = 25)No interim therapy (n = 12)Received interim therapy (n = 13)P
Median age at diagnosis (IQR, y) 43.6 (24.4-60.7) 42.0 (21.2-65.0) 43.6 (32.4-47.6) .46 
Age >45 y 12 (48.0%) 6 (50.0%) 6 (46.2%) .84 
Male sex 13 (52.0%) 5 (41.7%) 8 (61.5%) .32 
Median number of prior lines of therapy before blinatumomab (range, lines) 1 (1-5) 2 (1-3) 1 (1-5) .04 
Prior alloHSCT before mAb1 3 (12.0%) 1 (8.3%) 2 (15.4%) 1.00 
High-risk cytogenetic abnormalities 10 (40.0%) 4 (33.3%) 6 (46.2%) .21 
Philadelphia chromosome positive 4 (16.0%) 3 (25.0%) 1 (7.1%) .32 
Presence of MLL rearrangement 1 (4.0%) 1 (8.3%) 0 (0.0%) 1.00 
Disease burden at the time of blinatumomab mAb1    .59 
 MRD 7 (28.0%) 4 (33.3%) 3 (23.1%)  
 Morphologic disease 18 (72.0%) 8 (66.7%) 10 (76.9%)  
Site of disease at the time of blinatumomab mAb1    .78 
 Isolated marrow 21 (84.0%) 10 (83.3%) 11 (84.6%)  
 Isolated extramedullary 1 (4.0%) 0 (0.0%) 1 (7.7%)  
 Both 3 (12.0%) 2 (16.7%) 1 (7.7%)  
Median no. of blinatumomab mAb1 cycles (range, cycles) 1 (1-6) 1 (1-6) 1 (1-4) .53 
Best response to blinatumomab mAb1    .32 
 CR 13 (52.0%) 5 (41.7%) 8 (61.5%)  
 No response 12 (48.0%) 7 (58.3%) 5 (38.5%)  
Median time from blinatumomab to progression/relapse (IQR, d) 73 (34-219) 65 (37-118) 73 (33-290) .85 
Site of disease at the time of relapse following blinatumomab mAb1    .41 
 Isolated marrow 15 (60.0%) 8 (66.7%) 7 (53.8%)  
 Isolated extramedullary 1 (4.0%) 1 (8.3%) 0 (0.0%)  
 Both 9 (36.0%) 3 (25.0%) 6 (46.2%)  
Central nervous system involvement at the time of relapse after blinatumomab mAb1 1 (4.0%) 0 (0.0%) 1 (7.7%) .48 
Response to inotuzumab mAb2    .89 
 CR 17 (68.0%) 8 (69.2%) 9 (69.2%)  
 No response 8 (32.0%) 4 (30.8%) 4 (30.8%)  

MLL, mixed lymphoid lineage.

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