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. 2024 Apr 29;19(3):321–332. doi: 10.1007/s11523-024-01054-z

Table 2.

Summary of adverse events (AEs), as-treated population

Patients with n (%) AML (n = 27) MM (n = 18) DLBCL (n = 22) Total (N = 67)
At least one AE 26 (96.3) 18 (100.0) 22 (100.0) 66 (98.5)
 At least one treatment-related AE 17 (63.0) 17 (94.4) 18 (81.8) 52 (77.6)
 At least one grade 3-4 AE 23 (85.2) 15 (83.3) 19 (86.4) 57 (85.1)
 At least one grade 3-4 treatment-related AE 13 (48.1) 14 (77.8) 16 (72.7) 43 (64.2)
 At least one serious AE 18 (66.7) 6 (33.3) 10 (45.5) 34 (50.7)
 Treatment-related death 1 (3.7) 0 0 1 (1.5)
At least one AE leading to discontinuation 6 (22.2) 9 (50.0) 8 (36.4) 23 (34.3)
At least one treatment-related AE leading to discontinuation 3 (11.1) 7 (38.9) 6 (27.3) 16 (23.9)
At least one AE leading to dose interruption 0 1 (5.6) 0 1 (1.5)
At least one treatment-related AE leading to dose interruption 0 1 (5.6) 0 1 (1.5)
At least one AE leading to dose delay 8 (29.6) 8 (44.4) 10 (45.5) 26 (38.8)
At least one treatment-related AE leading to dose delay 5 (18.5) 8 (44.4) 9 (40.9) 22 (32.8)
At least one AE leading to dose omission 4 (14.8) 9 (50.0) 10 (45.5) 23 (34.3)
At least one treatment-related AE leading to dose omission 3 (11.1) 9 (50.0) 10 (45.5) 22 (32.8)

AML acute myeloid leukemia, DLBCL diffuse large B-cell lymphoma, MM multiple myeloma