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. Author manuscript; available in PMC: 2020 Jun 15.
Published in final edited form as: CNS Drugs. 2018 Dec;32(12):1091–1101. doi: 10.1007/s40263-018-0582-9

Table 2.

Neurotoxicity in selected non-CD I9-directed chimeric antigen receptor (CAR) T cells for hematologic malignancies

References (first author, year) NCI N Age group CAR target CAR construct Disease CRR (%) sNT (%) NT (%) CRS (%) sCRS (%) toci (%) steroids (%)
Fry. 2018 [28] NCT02315612 21 Peds. adult CD22 4-IBB ALL (majority CD19 CAR pretreated) 57a
43b
0 25 76 0 0 0
Ramos, 2017 [27] NCT01316146 9 Adult CD30 28z HL, ALCL 33 0 0 0 0 n/a n/a
Wang. 2017 [29] NCT02259556 18 Peds, adult CD30 4-IBB HL 0 0 0 0 0 n/a n/a
Ali. 2016 [30] NCT02215967 12 Adult BCMA 28z MM 8 8 25 50 25 33 0
Ritchie. 2013 [3 1] CTX 08-0002 4 Adult LeY 28z AML 25 0 0 25 0 0 0

4–1BB 4–1BB co-stimulatory domain, 28z CD28 co-stimulatory domain. ALCL anaplastic large cell lymphoma. ALL acute lymphoblastic leukemia. AML acute myelogenous leukemia, BCMA B-cell maturation antigen. CRR complete remission rate. CRS cytokine release syndrome. HL Hodgkin’s lymphoma, MM multiple myeloma. n/a not available. NCI’ national clinical trial. NT neurotoxicity. peds pediatrics, sCRS severe CRS, sNT severe neurotoxicity (Common Terminology Criteria for Adverse Events grade 3 or higher), steroids corticosteroids. foci tocilizumab

a

Morphologic remission

b

Minimal residual disease-negative remission