Table 2.
Patients (N = 14) | |
---|---|
CD19 expression on lymphoma cells after loncastuximab tesirine therapy, n (%) | |
Positive | 10 (71) |
Not checked | 4 (29) |
Median interval between loncastuximab tesirine and CAR T-cell therapy (range), d | 120 (22-600) |
Additional therapy between loncastuximab tesirine and CAR T-cell therapy, n (%) | |
Yes* | 6 (43) |
No | 8 (57) |
Disease status before CAR T-cell therapy, n (%) | |
Refractory disease | 5 (36) |
Progressive disease | 8 (57) |
Partial remission | 1 (7) |
Flu/Cy lymphodepletion, n (%) | 14 (100) |
Type of CAR T-cell therapy, n (%) | |
Axicabtagene ciloleucel | 5 (36) |
Tisagenlecleucel | 2 (14) |
Investigational targeting CD19† | 4 (29) |
JCAR017 | 3 (21) |
Best response to CAR T-cell therapy, n (%) | |
Complete response | 6 (43) |
Partial response | 1 (7) |
Refractory disease | 7 (50) |
CRS grade, n (%) | |
None | 6 (43) |
1 | 3 (21) |
2 | 4 (29) |
3 | 1 (7) |
ICANS grade, n (%) | |
None | 8 (57) |
1 | 4 (29) |
2 | 1 (7) |
3 | 0 (0) |
4 | 1 (7) |
CRS, cytokine release syndrome; Flu/Cy, lymphodepletion with fludarabine/cyclophosphamide.
Additional therapy between loncastuximab tesirine and CAR T-cell therapy included radiation alone (n = 3), radiation, ifosphamide/vinblastine/etoposide (n = 1), radiation; rituximab/methotrexate (n = 1), lenalidomide, anti-CD47 antibody, ibrutinib (n = 1).
One patient each received a CD19/CD22-directed CAR, and a CD19/CD20-directed CAR. Neither patient responded to CAR treatment.