Table 2.

Adverse events following CART-ddBCMA infusion


Event
Cohort
100 × 106 (N = 6) n (%)300 × 106 (N = 6) n (%)Total (N = 12) n (%)
Subjects with at least 1 ≥grade 3 AE, % 6 (100) 6 (100) 12 (100) 
Neutropenia, % 6 (100) 5 (83.3) 11 (91.7) 
Anemia, % 5 (83.3) 5 (83.3) 10 (83.3) 
Lymphocytopenia, % 5 (83.3) 3 (50.0) 8 (66.7) 
Thrombocytopenia, % 2 (33.3) 4 (66.7) 6 (50.0) 
Leukopenia, % 3 (50.0) 2 (33.3) 5 (41.7) 
Hyponatremia, % 2 (33.3) 2 (16.7) 
Febrile neutropenia, % 3 (50.0) 1 (16.7) 4 (33.3) 
Hypertension, % 2 (33.3) 1 (16.7) 3 (25.0) 

Event
Cohort
100 × 106 (N = 6) n (%)300 × 106 (N = 6) n (%)Total (N = 12) n (%)
Subjects with at least 1 ≥grade 3 AE, % 6 (100) 6 (100) 12 (100) 
Neutropenia, % 6 (100) 5 (83.3) 11 (91.7) 
Anemia, % 5 (83.3) 5 (83.3) 10 (83.3) 
Lymphocytopenia, % 5 (83.3) 3 (50.0) 8 (66.7) 
Thrombocytopenia, % 2 (33.3) 4 (66.7) 6 (50.0) 
Leukopenia, % 3 (50.0) 2 (33.3) 5 (41.7) 
Hyponatremia, % 2 (33.3) 2 (16.7) 
Febrile neutropenia, % 3 (50.0) 1 (16.7) 4 (33.3) 
Hypertension, % 2 (33.3) 1 (16.7) 3 (25.0) 
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