Table 3.

Results of pretransplantation treatments (from IND1 to C2-1)

Treatmentn (%)Result
IND1   
 n of patients 78  
 Rasburicase 25 (32.1)  
 Thrombomodulin-α 23 (29.5)  
 Dasatinib, dose down 6 (7.7) Transaminase elevation (n = 4), skin rash (n = 2) 
 Average total dose (SD), % of planned 3920 mg 94 (13.6)  
 D 8 PB blast <5% 34 (43.6)  
 D 22 PB blast <5% 73 (93.6)  
 D 42 response (CR + CRi) 78 (100)  
 CR 74 (94.9)  
 CRi 4 (5.1)  
 MRD negative* 17 (21.8) of 78  
IND2   
 n of patients 77  
 Delay of start 13 (16.8) Myelosuppression (n = 5), infection (n = 5), transaminase elevation (n = 1), social (n = 2) 
 Dasatinib, dose down 3 (3.9) FN (n = 1), unknown (n = 1), dose down as IND1 (n = 1) 
 Average total dose (SD), % of planned 2713 mg 96.9 (14.6)  
 MR* 41 (56.2) of 73  
 Proceeded to HSCT 2 (2.6)  
C1-1   
 n of patients 71  
 Delay of start 20 (28.2) Neutropenia (n = 8), infection (n = 4), liver damage (n = 2), social (n = 2), patient decision (n = 4) 
 Dasatinib, dose down 8 (11.3) Transaminase elevation (n = 3), other toxicities (n = 3), bridged to HSCT (n = 2) 
 Average total dose (SD), % of planned 2100 mg 94.9 (16.1)  
 MR* 45 (63.4) of 71  
 Proceeded to HSCT 21 (26.9)  
C2-1   
 n of patients 45  
 Delay of start 6 (13.3) Thrombocytopenia (n = 2), bridging to HSCT (n = 2), herpes infection (n = 1), patient decision (n = 1) 
 Dasatinib, dose down 5 (11.1) Transaminase elevation (n = 1), as previous course (n = 2), bridging to HSCT (n = 1), relapse (n = 1) 
 Average total dose (SD), % of planned 2100 mg 91 (4.6)  
 MRD negative* 24 (64.9) of 37  
 Proceeded to HSCT 18 (23.1)  
Treatmentn (%)Result
IND1   
 n of patients 78  
 Rasburicase 25 (32.1)  
 Thrombomodulin-α 23 (29.5)  
 Dasatinib, dose down 6 (7.7) Transaminase elevation (n = 4), skin rash (n = 2) 
 Average total dose (SD), % of planned 3920 mg 94 (13.6)  
 D 8 PB blast <5% 34 (43.6)  
 D 22 PB blast <5% 73 (93.6)  
 D 42 response (CR + CRi) 78 (100)  
 CR 74 (94.9)  
 CRi 4 (5.1)  
 MRD negative* 17 (21.8) of 78  
IND2   
 n of patients 77  
 Delay of start 13 (16.8) Myelosuppression (n = 5), infection (n = 5), transaminase elevation (n = 1), social (n = 2) 
 Dasatinib, dose down 3 (3.9) FN (n = 1), unknown (n = 1), dose down as IND1 (n = 1) 
 Average total dose (SD), % of planned 2713 mg 96.9 (14.6)  
 MR* 41 (56.2) of 73  
 Proceeded to HSCT 2 (2.6)  
C1-1   
 n of patients 71  
 Delay of start 20 (28.2) Neutropenia (n = 8), infection (n = 4), liver damage (n = 2), social (n = 2), patient decision (n = 4) 
 Dasatinib, dose down 8 (11.3) Transaminase elevation (n = 3), other toxicities (n = 3), bridged to HSCT (n = 2) 
 Average total dose (SD), % of planned 2100 mg 94.9 (16.1)  
 MR* 45 (63.4) of 71  
 Proceeded to HSCT 21 (26.9)  
C2-1   
 n of patients 45  
 Delay of start 6 (13.3) Thrombocytopenia (n = 2), bridging to HSCT (n = 2), herpes infection (n = 1), patient decision (n = 1) 
 Dasatinib, dose down 5 (11.1) Transaminase elevation (n = 1), as previous course (n = 2), bridging to HSCT (n = 1), relapse (n = 1) 
 Average total dose (SD), % of planned 2100 mg 91 (4.6)  
 MRD negative* 24 (64.9) of 37  
 Proceeded to HSCT 18 (23.1)  

CRi, CR with incomplete blood count recovery; FN, febrile neutropenia; PB, peripheral blood; SD, standard deviation.

*

Percentage of those tested.

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