Skip to main content
. 2021 Oct 28;139(12):1794–1806. doi: 10.1182/blood.2021011895

Table 2.

TEAEs reported at all dose levels

Any grade* Grade ≥3
Total
(n = 23)
Total
(n = 23)
Dose level 1
(n = 9)
Dose level 2
(n = 14)
Patients with any TEAE 23 (100) 22 (96) 8 (89) 14 (100)
Anemia 19 (83) 17 (74) 6 (67) 11 (79)
Cytokine release syndrome 17 (74) 2 (9) 0 2 (14)
Thrombocytopenia 17 (74) 16 (70) 4 (44) 12 (86)
Neutropenia/Neutrophil count decrease 16 (70) 16 (70) 5 (56) 11 (79)
Leukopenia 11 (48) 10 (43) 4 (44) 6 (43)
Pyrexia 10 (43) 0 0 0
Hypokalemia 9 (39) 0 0 0
Diarrhea 8 (35) 0 0 0
Hypophosphatemia 8 (35) 5 (22) 0 5 (36)
Nausea 8 (35) 0 0 0
Chills 7 (30) 0 0 0
Headache 7 (30) 0 0 0
Tremor 7 (30) 0 0 0
Acute kidney injury 6 (26) 1 (4) 1 (11) 0
Decreased appetite 6 (26) 0 0 0
Febrile neutropenia 6 (26) 6 (26) 0 6 (43)
Hypomagnesemia 6 (26) 0 0 0
Hyponatremia 6 (26) 0 0 0
Lymphopenia 6 (26) 6 (26) 2 (22) 4 (29)
Confusional state 5 (22) 2 (9) 0 2 (14)
Encephalopathy 5 (22) 4 (17) 1 (11) 3 (21)
Hypogammaglobulinemia 5 (22) 0 0 0
Insomnia 5 (22) 0 0 0

Data are expressed as n (%).

*

Table shows TEAEs in ≥20% of patients and all corresponding grade ≥3 TEAEs. A TEAE was any AE reported within 90 d of liso-cel administration. Any AE that occurred after initiation of another anticancer treatment was not considered a TEAE.

Listing of any grade in >10% of patients and all grade ≥3 TEAEs are shown in supplemental Tables 5 and 6.