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. 2020 Aug 14;4(16):3850–3852. doi: 10.1182/bloodadvances.2020002587

Table 2.

CAR T-cell therapy in DLBCL patients failing CD19-directed treatment

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.