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. 2019 Mar 25;11:2393–2404. doi: 10.2147/CMAR.S163225

Table 2.

Comparison of commercially developed anti-CD19 CAR T-cell compounds

Axicabtagene ciloleucel (KTE019) Tisagenlecleucel (CTL019) Lisocabtagene Maraleucel (JCAR017)
Structure
Anti-CD19 domain FCM63 FCM63 FCM63
Costimulatory domain CD28 4-1BB 4-1BB
Viral transfection Gamma-retrovirus Lentivirus Lentivirus
Target Cells PMBCs PMBCs CD4:CD8 ratio = 1
Phase-II clinical trial ZUMA-127 JULIET42 TRANSCEND43
Patient characteristics
Indication DLBCL, tFL, PMBCL
Refractory disease:
(1) PD or SD to most recent chemotherapy (2) PD or relapse within 12 months after ASCT
DLBCL, tFL
(1) after at least two lines of therapy
(2) either relapsed after or ineligible for ASCT
DLBCL, tFL, PMBCL, FL3b
(1) after two lines of treatment
(2) MCL after one line of treatment
Refractory to last treatment 74% 55% 67%
Patients included 111 165 134
Patients infused 101 111 114
Time from leuka-pheresis/enrolment to reinfusion 17 days 54 days n.a.
Efficacy
Best OR/best CR OR 82% CR 54% OR 52% CR 40% OR 75% CR 55%
CR after 6 months 40% 29% 34%
Toxicity
CRS grade 3–5 13% 22% 1%
Tocilizumab usage 43% 14% 12%
CRES grade 3–5 28% 12% 12%
Duration of response 11 months
(3.9 months; NR)36
NR
(181; 527 days)
NR
(5 months; NR)

Abbreviations: PMBC, peripheral blood mononuclear cells; PD, progressive disease; SD, stable disease; DLBCL, diffuse large B-cell lymphoma; tFL, transformed follicular lymphoma; PMBCL, peripheral mediastinal B-cell lymphoma; FL3b, follicular lymphoma grade 3b; ASCT, autologous stem cell transplantation; OR, overall response; CR, complete response; CRS, cytokine release syndrome; CRES, CAR related encephalopathy syndrome; NR, not reached.