Table 1.

Baseline and on-treatment characteristics of responding patients

CharacteristicsAll
(N = 130)
Transient response
(N = 46)
Durable response
(N = 83)
P
Age, y, median (range) 59.0 (18-78) 60.5 (18-78) 57.0 (19-77) .71 
Sex, male, no. (%) 80 (61.5) 33 (71.7) 46 (55.4) .068 
Stage, III/IV (vs I/II), no. (%) 96 (73.8) 33 (71.7) 62 (74.7) .71 
ECOG PS preinfusion, no. (%)    .72* 
 2 vs 0 to 1 9 (6.9) 4 (8.7) 5 (6.0)  
Extranodal involvement, no. (%)    .99 
 2 or more sites 28 (21.5) 10 (21.7) 18 (21.7)  
Bulk (≥7.5 cm) 30 (23.1) 14 (30.4) 16 (19.3) .15 
COO, no. (%), n = 97    .19 
 Non-GCB (vs GCB) 40 (41.2) 10 (31.3) 29 (45.3)  
Double/triple hit, no. (%), n = 108    .67 
 Double/triple hit (vs none) 13 (12.0) 6 (15.8) 7 (10.1)  
 Double/triple expressor (vs none) 16 (14.8) 5 (13.2) 11 (15.9)  
Refractory to last treatment, no. (%) 86 (66.2) 32 (69.6) 53 (63.9) .51 
Bridging therapy, no. (%)    .83* 
 Systemic 67 (51.5) 25 (54.3) 42 (50.6)  
 RT 30 (23.1) 9 (19.6) 20 (24.1)  
 Combined modality 5 (3.8) 1 (2.2) 4 (4.8)  
LDH preinfusion, no. (%), n = 104    .041† 
 >ULN (vs normal) 50 (48.1) 20 (55.6) 29 (43.3)  
 >2 ULN (vs normal) 12 (11.5) 6 (16.7) 6 (9.0)  
CRP preinfusion, median (range), n = 104 11.2 (0.5-235) 22.5 (1-235) 6.8 (0.5-160) .003 
CAR-T product, no. (%)     
 Axi-cel 107 (82.3) 39 (84.8) 67 (80.7) .56 
 Tisa-cel 23 (17.7) 7 (15.2) 16 (19.3)  
Grade ≥3 CAR-T toxicity, no. (%)     
 CRS 11 (8.5) 6 (13.0) 5 (6.0) .20* 
 ICANS 22 (16.9) 8 (17.4) 13 (15.7) .80 
DS at 1 mo, no. (%)     
 DS 1-2 40 (30.8) 6 (13.0) 34 (41.0) <.0001 
 DS 3 31 (23.8) 10 (21.7) 21 (25.3)  
 DS 4 46 (35.4) 17 (37.0) 28 (33.7)  
 DS 5 13 (10.0) 13 (28.3)  
CharacteristicsAll
(N = 130)
Transient response
(N = 46)
Durable response
(N = 83)
P
Age, y, median (range) 59.0 (18-78) 60.5 (18-78) 57.0 (19-77) .71 
Sex, male, no. (%) 80 (61.5) 33 (71.7) 46 (55.4) .068 
Stage, III/IV (vs I/II), no. (%) 96 (73.8) 33 (71.7) 62 (74.7) .71 
ECOG PS preinfusion, no. (%)    .72* 
 2 vs 0 to 1 9 (6.9) 4 (8.7) 5 (6.0)  
Extranodal involvement, no. (%)    .99 
 2 or more sites 28 (21.5) 10 (21.7) 18 (21.7)  
Bulk (≥7.5 cm) 30 (23.1) 14 (30.4) 16 (19.3) .15 
COO, no. (%), n = 97    .19 
 Non-GCB (vs GCB) 40 (41.2) 10 (31.3) 29 (45.3)  
Double/triple hit, no. (%), n = 108    .67 
 Double/triple hit (vs none) 13 (12.0) 6 (15.8) 7 (10.1)  
 Double/triple expressor (vs none) 16 (14.8) 5 (13.2) 11 (15.9)  
Refractory to last treatment, no. (%) 86 (66.2) 32 (69.6) 53 (63.9) .51 
Bridging therapy, no. (%)    .83* 
 Systemic 67 (51.5) 25 (54.3) 42 (50.6)  
 RT 30 (23.1) 9 (19.6) 20 (24.1)  
 Combined modality 5 (3.8) 1 (2.2) 4 (4.8)  
LDH preinfusion, no. (%), n = 104    .041† 
 >ULN (vs normal) 50 (48.1) 20 (55.6) 29 (43.3)  
 >2 ULN (vs normal) 12 (11.5) 6 (16.7) 6 (9.0)  
CRP preinfusion, median (range), n = 104 11.2 (0.5-235) 22.5 (1-235) 6.8 (0.5-160) .003 
CAR-T product, no. (%)     
 Axi-cel 107 (82.3) 39 (84.8) 67 (80.7) .56 
 Tisa-cel 23 (17.7) 7 (15.2) 16 (19.3)  
Grade ≥3 CAR-T toxicity, no. (%)     
 CRS 11 (8.5) 6 (13.0) 5 (6.0) .20* 
 ICANS 22 (16.9) 8 (17.4) 13 (15.7) .80 
DS at 1 mo, no. (%)     
 DS 1-2 40 (30.8) 6 (13.0) 34 (41.0) <.0001 
 DS 3 31 (23.8) 10 (21.7) 21 (25.3)  
 DS 4 46 (35.4) 17 (37.0) 28 (33.7)  
 DS 5 13 (10.0) 13 (28.3)  

Exclusion of n = 1 patient with nonrelapse death prior to 3-mo assessment (not evaluable for durability of response). P values are Wilcoxon Mann-Whitney (continuous) or χ2 (discrete, except *Fisher’s exact test and χ2 for trend).

COO, cell of origin; CRS, cytokine release syndrome; GCB, germinal center B-cell; ICANS, immune effector cell-associated neurotoxicity syndrome; ULN, upper limit of normal.

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