Table 1

Grade ≥3 treatment-emergent adverse events during the study

Grade ≥3 adverse events2.5 × 106 CAR-BCMA/kg (n = 3)5.0 × 106 CAR-BCMA/kg (n = 11)7.5 × 106 CAR-BCMA/kg (n = 1)Total (n = 15)
Hematologic toxicities, n (%)
 Neutropenia3 (100.0)10 (90.9)114 (93.3)
 Leukopenia3 (100.0)8 (72.7)112 (80.0)
 Lymphopenia2 (66.7)8 (72.7)111 (73.3)
 Anemia2 (66.7)6 (54.5)19 (60.0)
 Thrombocytopenia03 (27.3)14 (26.7)
 Myelosuppression01 (9.1)01 (6.7)
Infectious disease, n (%)
 Infection02 (18.2)13 (20)
 Upper respiratory infection01 (9.1)01 (6.7)
 Escherichia sepsis01 (9.1)01 (6.7)
 Infectious enterocolitis01 (9.1)01 (6.7)
 Pneumonia01 (9.1)01 (6.7)
Metabolic and nutritional diseases, n (%)
 Hypokalemia02 (18.2)02 (13.3)
Kidney and urological diseases, n (%)
 Renal calculus01 (9.1)01 (6.7)
Others, n (%)
 Hypofibrinogenemia01 (9.1)01 (6.7)
 Ferritin increased1 (33.3)1 (9.1)02 (13.3)
 Interleukin increased01 (9.1)01 (6.7)

CAR-T, chimeric antigen receptor T cell; BCMA, B cell maturation antigen.