Demographic and clinical characteristics of patients at time of lymphodepleting chemotherapy
Characteristics . | Patients (n = 47) . |
---|---|
Age, median (range), y | 65 (31-82) |
Male sex, no. (%) | 31 (66) |
ECOG performance status >1, no. (%) | 4 (9) |
Disease stage III or IV, no. (%) | 42 (89) |
Histology, no. (%) | |
DLBCL NOS | 38 (81) |
tFL | 5 (11) |
THRLBCL | 2 (4) |
PMBL | 1 (2) |
HGBL | 1 (2) |
No. of prior therapies, median (range)∗ | 3 (2-9) |
Previous ASCT, no. (%) | 9 (19) |
Bulky disease (>5 cm), no. (%) | 17 (36) |
CRP ≥30 mg/L, no. (%)† | 18 (39) |
LDH ≥2 × ULN, no. (%) | 27 (57) |
CAR T-cell therapy, no. (%) | |
Axi-cel | 22 (47) |
Tisa-cel | 20 (42) |
Liso-cel | 5 (11) |
Time from the last BsAb dose to leukapheresis, median (range), d | 51 (13-512) |
Time from the last BsAb dose to CAR T-cell infusion, median (range), d | 97 (47-572) |
Time from leukapheresis to CAR T-cell infusion, median (range), d | 43 (34-103) |
Bridging therapy, no. (%) | 42 (89) |
Immunochemotherapy | 29 (62) |
Targeted therapy | 9 (19) |
Radiotherapy | 3 (6) |
Not specified | 1 (2) |
Response to bridging, no. (%)‡ | |
Responder (CR/PR) | 11 (28) |
Nonresponder (SD/PD) | 28 (72) |
Prior BsAb exposure | |
Type of BsAb, no. (%)§ | |
CD20/CD3 | 43 (91) |
CD22/CD3 | 4 (9) |
Combination with BsAb, no. (%) | 5 (11) |
Lenalidomide | 2 (4) |
Chemotherapy | 2 (4) |
Polatuzumab vedotin | 1 (2) |
Missing | 1 (2) |
Characteristics . | Patients (n = 47) . |
---|---|
Age, median (range), y | 65 (31-82) |
Male sex, no. (%) | 31 (66) |
ECOG performance status >1, no. (%) | 4 (9) |
Disease stage III or IV, no. (%) | 42 (89) |
Histology, no. (%) | |
DLBCL NOS | 38 (81) |
tFL | 5 (11) |
THRLBCL | 2 (4) |
PMBL | 1 (2) |
HGBL | 1 (2) |
No. of prior therapies, median (range)∗ | 3 (2-9) |
Previous ASCT, no. (%) | 9 (19) |
Bulky disease (>5 cm), no. (%) | 17 (36) |
CRP ≥30 mg/L, no. (%)† | 18 (39) |
LDH ≥2 × ULN, no. (%) | 27 (57) |
CAR T-cell therapy, no. (%) | |
Axi-cel | 22 (47) |
Tisa-cel | 20 (42) |
Liso-cel | 5 (11) |
Time from the last BsAb dose to leukapheresis, median (range), d | 51 (13-512) |
Time from the last BsAb dose to CAR T-cell infusion, median (range), d | 97 (47-572) |
Time from leukapheresis to CAR T-cell infusion, median (range), d | 43 (34-103) |
Bridging therapy, no. (%) | 42 (89) |
Immunochemotherapy | 29 (62) |
Targeted therapy | 9 (19) |
Radiotherapy | 3 (6) |
Not specified | 1 (2) |
Response to bridging, no. (%)‡ | |
Responder (CR/PR) | 11 (28) |
Nonresponder (SD/PD) | 28 (72) |
Prior BsAb exposure | |
Type of BsAb, no. (%)§ | |
CD20/CD3 | 43 (91) |
CD22/CD3 | 4 (9) |
Combination with BsAb, no. (%) | 5 (11) |
Lenalidomide | 2 (4) |
Chemotherapy | 2 (4) |
Polatuzumab vedotin | 1 (2) |
Missing | 1 (2) |
ASCT, autologous stem cell transplant; Axi-cel, axicabtagene ciloleucel; CR, complete response; CRP, C-reactive protein; DLBCL, diffuse large B-cell lymphoma; ECOG, Eastern Cooperative Oncology Group; HGBL, high-grade B-cell lymphoma; LDH, lactate dehydrogenase; Liso-cel, lisocabtagene maraleucel; NOS, not otherwise specified; PD, progressive disease; PMBL, primary mediastinal B-cell lymphoma; PR, partial response; SD, stable disease; tFL, transformed follicular lymphoma; THRLBCL, T-cell histiocyte-rich large B-cell lymphoma; Tisa-cel, tisagenlecleucel; ULN, upper limit of normal.
The median number of prior lines of therapy before BsAbs was 2 (range, 1-6).
Missing data for 1 patient.
Evaluable response in 39 patients (3 patients with missing data).
The CD20/CD3 bispecifics (n = 43/47) included glofitamab (n = 23), epcoritamab (n = 3), mosunetuzumab (n = 8), odronextamab (n = 6), and plamotamab (n = 3).