Table 3

Selected adverse events

Patients, n (%)G-FC (n = 21)G-B (n = 20)
All gradesGrade 3-4All gradesGrade 3-4
All AEs 21 (100) 18 (86) 20 (100) 17 (85) 
Hematologic AE  
 Neutropenia 6 (29) 6 (29) 10* (50) 10 (50) 
 Febrile neutropenia 4 (19) 4 (19) 2* (10) 2 (10) 
 Thrombocytopenia 4 (19) 4 (19) 4 (20) 2 (10) 
 Anemia 5 (24) 3 (14) 3 (15) 1 (5) 
Infections 11 (52) 4 (19) 9 (45) 1 (5) 
Tumor lysis syndrome 1 (5) 1 (5) 
Laboratory investigations  
 Elevation in hepatic transaminases 4 (19) 4 (19) 2 (10) 2 (10) 
Patients, n (%)G-FC (n = 21)G-B (n = 20)
All gradesGrade 3-4All gradesGrade 3-4
All AEs 21 (100) 18 (86) 20 (100) 17 (85) 
Hematologic AE  
 Neutropenia 6 (29) 6 (29) 10* (50) 10 (50) 
 Febrile neutropenia 4 (19) 4 (19) 2* (10) 2 (10) 
 Thrombocytopenia 4 (19) 4 (19) 4 (20) 2 (10) 
 Anemia 5 (24) 3 (14) 3 (15) 1 (5) 
Infections 11 (52) 4 (19) 9 (45) 1 (5) 
Tumor lysis syndrome 1 (5) 1 (5) 
Laboratory investigations  
 Elevation in hepatic transaminases 4 (19) 4 (19) 2 (10) 2 (10) 
*

The total number of patients treated with G-B who experienced grade 3-4 neutropenia was 11 (55%), as 1 patient was reported to have both febrile neutropenia and grade 3-4 neutropenia.

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