Table 1.

Baseline characteristics of patients by age group

Characteristic≥70 y<70 yP value
No. of patients, N 251 570  
Age at infusion, y   <.01  
Median (min-max) 74.3 (70.1-90.3) 61.6 (29.3-69.9)  
≥80, n (%) 14 (5.6) 0 (0.0)  
Sex, n (%)   .96  
Female 103 (41.0) 231 (40.5)  
Male 148 (59.0) 338 (59.3)  
Not reported 0 (0.0) 1 (0.2)  
Recipient race, n (%)   .13  
White 212 (84.5) 440 (77.2)  
Black or African American 28 (11.2) 92 (16.1)  
Asian 8 (3.2) 14 (2.5)  
Native Hawaiian or other Pacific Islander 1 (0.4) 1 (0.2)  
American Indian or Alaska Native 0 (0.0) 2 (0.4)  
>1 race 0 (0.0) 5 (0.9)  
Not reported 2 (0.8) 16 (2.8)  
Recipient ethnicity, n (%)   .08  
Hispanic or Latino 10 (4.0) 45 (7.9)  
Not Hispanic or Latino 235 (93.6) 516 (90.5)  
Not reported 6 (2.4) 9 (1.6)  
ECOG performance status category before infusion, n (%)   .18  
ECOG 0-1 215 (85.7) 513 (90.0)  
ECOG ≥2 16 (6.4) 26 (4.6)  
Not reported 20 (8.0) 31 (5.4)  
Clinically significant comorbidity, n (%)   .12  
No 47 (18.7) 142 (24.9)  
Yes 204 (81.3) 427 (74.9)  
Cytogenetic risk any time before infusion, n (%)   .57  
Standard risk 167 (66.5) 364 (63.9)  
High risk 54 (21.5) 142 (24.9)  
Not reported 30 (12.0) 64 (11.2)  
ISS stage before infusion, n (%)   .04  
52 (20.7) 158 (27.7)  
II 54 (21.5) 88 (15.4)  
III 25 (10.0) 43 (7.5)  
Not reported 120 (47.8) 281 (49.3)  
Extramedullary plasmacytomas, n (%)   .06  
No 123 (49.0) 280 (49.1)  
Yes 17 (6.8) 68 (11.9)  
Not reported 111 (44.2) 222 (38.9)  
Plasma cells in bone marrow >50% before infusion, n (%)   .11  
No 140 (55.8) 297 (52.1)  
Yes 27 (10.8) 44 (7.7)  
Not reported 84 (33.5) 229 (40.2)  
Penta-exposed before infusion, n (%)   .28  
No 97 (38.6) 233 (40.9)  
Yes 153 (61.0) 337 (59.1)  
Not reported 1 (0.4) 0 (0.0)  
Triple-class exposed before infusion, n (%)   .38  
No 14 (5.6) 30 (5.3)  
Yes 236 (94.0) 540 (94.7)  
Not reported 1 (0.4) 0 (0.0)  
Prior BCMA therapy, n (%)   .56  
No 213 (84.9%) 494 (86.6%)  
Yes 39 (15.5%) 80 (14.1%)  
Lymphodepleting chemotherapy regimen, n (%)   .04  
Cyclophosphamide + fludarabine 217 (86.5) 524 (91.9)  
Bendamustine 22 (8.8) 29 (5.1)  
Other 11 (4.4) 17 (3.0)  
Not reported 1 (0.4) 0 (0.0)  
Disease status before infusion, n (%)   .79  
CR/stringent CR 4 (1.6) 13 (2.3)  
VGPR 17 (6.8) 42 (7.4)  
PR 28 (11.2) 68 (11.9)  
NR/SD, PD, and relapse from CR 200 (79.7) 445 (78.1)  
Not reported 2 (0.8) 2 (0.4)  
Hemoglobin <8 g/dL before infusion, n (%)   .24  
No 217 (86.5) 471 (82.6)  
Yes 30 (12.0) 79 (13.9)  
Not reported 4 (1.6) 20 (3.5)  
Platelets <50 × 109/L before infusion, n (%)   .33  
No 219 (87.3) 479 (84.0)  
Yes 27 (10.8) 69 (12.1)  
Not reported 5 (2.0) 22 (3.9)  
ANC <1000 × 106/L before infusion, n (%)   .66§  
No 222 (88.4) 502 (88.1)  
Yes 17 (6.8) 33 (5.8)  
Not reported 12 (4.8) 35 (6.1)  
Total no. of cells administered, median (range), ×106 410 (312-460) 409 (307-460) .79  
Total no. of administered cells ≥400 × 106, n (%)   .97§  
No 145 (57.8) 330 (57.9)  
Yes 101 (40.2) 230 (40.4)  
Not reported 5 (2.0) 10 (1.8)  
Characteristic≥70 y<70 yP value
No. of patients, N 251 570  
Age at infusion, y   <.01  
Median (min-max) 74.3 (70.1-90.3) 61.6 (29.3-69.9)  
≥80, n (%) 14 (5.6) 0 (0.0)  
Sex, n (%)   .96  
Female 103 (41.0) 231 (40.5)  
Male 148 (59.0) 338 (59.3)  
Not reported 0 (0.0) 1 (0.2)  
Recipient race, n (%)   .13  
White 212 (84.5) 440 (77.2)  
Black or African American 28 (11.2) 92 (16.1)  
Asian 8 (3.2) 14 (2.5)  
Native Hawaiian or other Pacific Islander 1 (0.4) 1 (0.2)  
American Indian or Alaska Native 0 (0.0) 2 (0.4)  
>1 race 0 (0.0) 5 (0.9)  
Not reported 2 (0.8) 16 (2.8)  
Recipient ethnicity, n (%)   .08  
Hispanic or Latino 10 (4.0) 45 (7.9)  
Not Hispanic or Latino 235 (93.6) 516 (90.5)  
Not reported 6 (2.4) 9 (1.6)  
ECOG performance status category before infusion, n (%)   .18  
ECOG 0-1 215 (85.7) 513 (90.0)  
ECOG ≥2 16 (6.4) 26 (4.6)  
Not reported 20 (8.0) 31 (5.4)  
Clinically significant comorbidity, n (%)   .12  
No 47 (18.7) 142 (24.9)  
Yes 204 (81.3) 427 (74.9)  
Cytogenetic risk any time before infusion, n (%)   .57  
Standard risk 167 (66.5) 364 (63.9)  
High risk 54 (21.5) 142 (24.9)  
Not reported 30 (12.0) 64 (11.2)  
ISS stage before infusion, n (%)   .04  
52 (20.7) 158 (27.7)  
II 54 (21.5) 88 (15.4)  
III 25 (10.0) 43 (7.5)  
Not reported 120 (47.8) 281 (49.3)  
Extramedullary plasmacytomas, n (%)   .06  
No 123 (49.0) 280 (49.1)  
Yes 17 (6.8) 68 (11.9)  
Not reported 111 (44.2) 222 (38.9)  
Plasma cells in bone marrow >50% before infusion, n (%)   .11  
No 140 (55.8) 297 (52.1)  
Yes 27 (10.8) 44 (7.7)  
Not reported 84 (33.5) 229 (40.2)  
Penta-exposed before infusion, n (%)   .28  
No 97 (38.6) 233 (40.9)  
Yes 153 (61.0) 337 (59.1)  
Not reported 1 (0.4) 0 (0.0)  
Triple-class exposed before infusion, n (%)   .38  
No 14 (5.6) 30 (5.3)  
Yes 236 (94.0) 540 (94.7)  
Not reported 1 (0.4) 0 (0.0)  
Prior BCMA therapy, n (%)   .56  
No 213 (84.9%) 494 (86.6%)  
Yes 39 (15.5%) 80 (14.1%)  
Lymphodepleting chemotherapy regimen, n (%)   .04  
Cyclophosphamide + fludarabine 217 (86.5) 524 (91.9)  
Bendamustine 22 (8.8) 29 (5.1)  
Other 11 (4.4) 17 (3.0)  
Not reported 1 (0.4) 0 (0.0)  
Disease status before infusion, n (%)   .79  
CR/stringent CR 4 (1.6) 13 (2.3)  
VGPR 17 (6.8) 42 (7.4)  
PR 28 (11.2) 68 (11.9)  
NR/SD, PD, and relapse from CR 200 (79.7) 445 (78.1)  
Not reported 2 (0.8) 2 (0.4)  
Hemoglobin <8 g/dL before infusion, n (%)   .24  
No 217 (86.5) 471 (82.6)  
Yes 30 (12.0) 79 (13.9)  
Not reported 4 (1.6) 20 (3.5)  
Platelets <50 × 109/L before infusion, n (%)   .33  
No 219 (87.3) 479 (84.0)  
Yes 27 (10.8) 69 (12.1)  
Not reported 5 (2.0) 22 (3.9)  
ANC <1000 × 106/L before infusion, n (%)   .66§  
No 222 (88.4) 502 (88.1)  
Yes 17 (6.8) 33 (5.8)  
Not reported 12 (4.8) 35 (6.1)  
Total no. of cells administered, median (range), ×106 410 (312-460) 409 (307-460) .79  
Total no. of administered cells ≥400 × 106, n (%)   .97§  
No 145 (57.8) 330 (57.9)  
Yes 101 (40.2) 230 (40.4)  
Not reported 5 (2.0) 10 (1.8)  

ANC, absolute neutrophil count; CR, complete response; ECOG, Eastern Cooperative Oncology Group; IQR, interquartile range; max, maximum; min, minimum; NR, no response; PD, progressive disease; PR, partial response; SD, stable disease; VGPR, very good partial remission.

Fisher exact test.

Pearson χ2 test.

§

Kruskal-Wallis test.

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