Table 1.
All (n = 420) | Relapsed (n = 163∗) | |
---|---|---|
Demographics | ||
Female, n (%) | 156 (37.1) | 71 (37.1) |
Median age at B-ALL diagnosis, y (IQR) | 7.6 (3.4-13.8) | 7.3 (0.02-24.3) |
Median age at CAR infusion, y (IQR) | 12.7 (7.1-17.5) | 11.8 (0.8-30.4) |
Race (%) | ||
White | 275 (65.5) | 108 (66.2) |
Black | 17 (4.0) | 5 (3.1) |
Asian | 20 (4.8) | 8 (4.9) |
Other (mixed)/unknown | 108 (25.7) | 38 (23.3) |
Ethnicity (%) | ||
Non-Hispanic | 255 (60.7) | 109 (66.9) |
Hispanic | 134 (31.9) | 42 (25.8) |
Unknown | 31 (7.4) | 12 (7.4) |
Prior therapy (prior to CAR T cells) | ||
Primary refractory disease, n (%) | 92 (21.9) | 29 (17.8) |
No. of prior CR, median (range) | 2 (0-7) | 2 (0-7) |
Prior blinatumomab, n (%) | 33 (7.9) | 35 (21.5) |
Prior HSCT, n (%) | 159 (37.9) | 76 (46.6) |
Cytogenetics (%) | ||
Normal | 41 (9.8) | 18 (11) |
ETV6-RUNX1 | 24 (5.7) | 16 (9.8) |
KMT2Ar | 38 (9) | 15 (9.2) |
Ph+/Ph-like | 61 (14.5) | 17 (10.4) |
Hypodiploid | 12 (2.9) | 7 (4.3) |
Disease status pre-CAR (%) | ||
M1 or MRD-negative marrow | 217 (51.7) | 64 (39.3) |
M2/M3 marrow | 203 (48.3) | 99 (60.7) |
CNS3 | 4 (0.9) | 1 (0.01) |
Active EM disease | 22 (5.2) | 9 (5.5) |
Active PB blasts | 56 (13.3) | 30 (18.4) |
CAR T-cell construct infused (%)† | ||
CD19/4-1BB | 277 (66.0) | 115 (70.6) |
Tisagenlecleucel (Kymriah) | 88 (21.0) | 34 (20.9) |
CD19/28z | 55 (13.1) | 14 (8.6) |
Relapse phenotype (%) | ||
CD19pos | N/A | 83 (50.9) |
CD19neg | N/A | 68 (41.7) |
Lineage switch | N/A | 12 (7.4) |
Blina, blinatumomab; EM, extramedullary; KMT2Ar, KMT2A-rearranged; MRD, minimal residual disease (defined as <.01% bone marrow blasts by multiparameter flow cytometry); N/A, not applicable; PB, peripheral blood.
A total of 166 patients experienced relapse, but immunophenotype at relapse was only available in 163 patients, which constituted the analysis cohort.
4-1BB CAR T-cell constructs were comprised of 1 of 2 available constructs, including the construct that eventually was FDA approved; tisagenlecleucel refers to the commercially available construct.