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. 2023 Mar 31;29(10):1894–1905. doi: 10.1158/1078-0432.CCR-22-3136

Table 2.

Most common AEs, CRS, and neurologic events in patients ≥65 years.

Axi-Cel, N = 49 SOC, N = 55
n (%) Any grade Grade ≥3 Any grade Grade ≥3
Any AE 49 (100) 46 (94) 55 (100) 45 (82)
 Pyrexia 47 (96) 4 (8) 14 (25) 0
 Neutropeniaa 39 (80) 39 (80) 24 (44) 24 (44)
 Nausea 23 (47) 1 (2) 37 (67) 3 (5)
 Anemia 22 (45) 19 (39) 32 (58) 25 (45)
 Thrombocytopeniab 21 (43) 14 (29) 37 (67) 35 (64)
 Leukopeniac 19 (39) 18 (37) 10 (18) 10 (18)
 Fatigue 17 (35) 2 (4) 31 (56) 1 (2)
 Diarrhea 17 (35) 1 (2) 24 (44) 0
 Decreased appetite 18 (37) 2 (4) 19 (35) 2 (4)
 Hypokalemia 16 (33) 7 (14) 17 (31) 5 (9)
 Hypotension 23 (47) 6 (12) 8 (15) 1 (2)
 Constipation 9 (18) 0 21 (38) 0
 Headache 14 (29) 0 14 (25) 1 (2)
 Hypophosphatemia 20 (41) 15 (31) 8 (15) 7 (13)
 Cough 18 (37) 0 9 (16) 0
 Edema peripheral 9 (18) 0 15 (27) 1 (2)
 Vomiting 5 (10) 0 18 (33) 1 (2)
 Chills 18 (37) 0 4 (7) 0
 Hypocalcemia 16 (33) 0 6 (11) 0
 Sinus tachycardia 18 (37) 1 (2) 4 (7) 0
 Confusional state 19 (39) 6 (12) 2 (4) 0
 Hypoxia 15 (31) 8 (16) 6 (11) 4 (7)
 Hypomagnesemia 7 (14) 1 (2) 13 (24) 1 (2)
 Acute kidney injury 7 (14) 1 (2) 12 (22) 3 (5)
 Lymphocyte count decreased 10 (20) 10 (20) 7 (13) 7 (13)
 Alanine aminotransferase increased 10 (20) 1 (2) 4 (7) 1 (2)
 Hypoalbuminemia 10 (20) 1 (2) 4 (7) 0
 Encephalopathy 12 (24) 7 (14) 1 (2) 0
 Tremor 12 (24) 0 1 (2) 0
 Febrile neutropenia 0 0 12 (22) 12 (22)
 Hypogammaglobulinemia 10 (20) 0 1 (2) 0
 Aphasia 10 (20) 3 (6) 0 0
CRS 48 (98) 4 (8)
 Pyrexia 47 (98) 3 (6)
 Hypotension 21 (44) 5 (10)
 Sinus tachycardia 16 (33) 1 (2)
 Chills 13 (27) 0
 Hypoxia 12 (25) 6 (13)
 Headache 8 (17) 0
Neurologic events 32 (65) 13 (27) 14 (25) 1 (2)
 Confusional state 19 (39) 6 (12) 2 (4) 0
 Encephalopathy 12 (24) 7 (14) 1 (2) 0
 Tremor 12 (24) 0 1 (2) 0
 Aphasia 10 (20) 3 (6) 0 0
 Somnolence 5 (10) 3 (6) 2 (4) 0
 Delirium 1 (2) 1 (2) 4 (7) 1 (2)
 Paresthesia 0 0 5 (9) 0

Note: Shown are any adverse events of any grade that occurred in at least 20% of the patients in either the axi-cel arm or the SOC arm, as well as events of the CRS that occurred in at least 15% of the patients in the axi-cel arm and neurologic events of any grade that occurred in at least 15% of the patients in the axi-cel arm or at least 3% of those in the SOC arm. The severity of the CRS was graded according to Lee and colleagues (18). Neurologic events were identified with the use of a prespecified search list of preferred terms in the Medical Dictionary for Regulatory Activities, version 23.1, on the basis of known neurotoxic effects associated with anti-CD19 immunotherapy, and were specifically identified with the use of methods that were based on the phase II study of blinatumomab (19). The severity of all adverse events, including neurologic events and symptoms of the CRS, was graded with the use of the Common Terminology Criteria for Adverse Events, version 4.03, of the NCI.

aNeutropenia refers to the combined preferred terms of neutropenia and neutrophil count decreased.

bThrombocytopenia refers to the combined preferred terms of thrombocytopenia and platelet count decreased.

cLeukopenia refers to the combined preferred terms of leukopenia and white-cell count decreased.