Skip to main content
. Author manuscript; available in PMC: 2023 Sep 1.
Published in final edited form as: Cancer Discov. 2023 Mar 1;13(3):580–597. doi: 10.1158/2159-8290.CD-22-0964

Table 2.

treatment emergent adverse events

TEAE All Grades (%) Grade 1 (%) Grade 2 (%) Grade 3 (%) Grade 4 (%) Grade 5 (%)
Any 9 (100%) 9 (100%) 9 (100%) 8 (89%) 7 (78%) 1 (11%)
IRR 2 (22%) 2 (22%) 0 0 0 0
CRS 6 (67%) 6 (67%) 0 0 0 0
ICANS 0 0 0 0 0 0
Infection 0 0 0 0 0 0
Pain 4 (44%) 2 (22%) 0 2 (22%) 0 0
Fatigue 8 (89%) 8 (89%) 0 0 0 0
Hypotension 2 (22%) 0 1 (11%) 1 (11%) 0 0
Headache 2 (22%) 2 (22%) 0 0 0 0
ALT increased 1 (11%) 1 (11%) 0 0 0 0
AST increased 1 (11%) 0 1 (11%) 0 0 0
Anemia 9 (100%) 1 (11%) 5 (56%) 3 (33%) 0 0
Neutropenia 8 (89%) 1 (11%) 2 (22%) 0 5 (56%) 0
Thrombocytopenia 8 (89%) 3 (33%) 0 1 (11%) 4 (44%) 0
Nausea 6 (67%) 6 (67%) 0 0 0 0
Vomiting 2 (22%) 2 (22%) 0 0 0 0
Diarrhea 2 (22%) 2 (22%) 0 0 0 0
Hypocellular marrow 1 (11%) 0 0 0 0 1 (11%)

TEAE: Treatment emergent adverse event; IRR: infusion-related reaction; CRS: cytokine release syndrome; ICANS: immune effector cell-associated neurotoxicity syndrome; ALT: alanine transaminase; AST: aspartate transaminase