Table 1.

Patient characteristics

VariableOverall
N = 44
Low CMV IgG
N = 13
High CMV IgG
N = 31
P value
Age (y), median (range) at the time of CAR-T 64 (36-76) 63 (47-73) 64 (36-76) .32 
Sex, n (%)     
Female 15 (34.1) 5 (38.5) 10 (32.3) .74 
Male 29 (65.9) 8 (61.5) 21 (67.7)  
MM subtype, n (%)     
IgG 24 (54.5) 8 (61.5) 16 (51.6) 1.00 
IgA 8 (18.2) 2 (15.4) 6 (19.4)  
IgD 1 (2.3) 0 (0) 1 (3.2)  
Bence–Jones 11 (25.0) 3 (23.1) 8 (25.8)  
R2-ISS stage at CAR-T, n (%)     
Stage 1 6 (13.6)) 4 (30.8) 2 (6.5) .20 
Stage 2 14 (31.8) 3 (23.1) 11 (35.5)  
Stage 3 22 (50) 6 (46.2) 16 (51.6)  
Stage 4 1 (2.3) 0 (0) 1 (3.2)  
Unknown 1 (2.3) 0 (0) 1 (3.2)  
MyCARe, n (%)     
Low 12 (27.3) 5 (38.5) 7 (22.6) .49 
Intermediate 29 (65.9) 7 (53.8) 22 (71.0)  
High 3 (6.8) 1 (7.7) 2 (6.5)  
CMV IgG (AU/mL), median (range) 187.15 (20.6-250) 64.7 (20.6-113.2) 238.2 (115.6-250) <.001 
Previous treatment lines, median (range) 3 (2-10) 3 (2-6) 3 (2-10) .50 
Previous autologous stem cell transplantation, n (%) 26 (59.1) 9 (69.2) 17 (54.8) .51 
Extramedullary disease, n (%) 6 (14.3) 1 (7.7) 5 (17.2) .65 
Triple-class refractory, n (%) 33 (75.0) 12 (92.3) 21 (67.7) .13 
Penta refractory, n (%) 3 (6.8) 1 (7.7) 2 (6.5) 
High-risk cytogenetic abnormality until CAR-T therapy, n (%)     
High-risk 31 (72.1) 8 (61.5) 23 (74.2) .46 
del(17p) 13 (29.5) 3 (23.1) 10 (32.3) .72 
t(4;14) 9 (20.5) 2 (15.4) 7 (22.6) .70 
t(14;16) 1 (2.3) 1 (7.7) 0 (0) .21 
1q abnormality 28 (63.6) 7 (53.8) 21 (67.7) .30 
Tocilizumab use for CRS, n (%) 44 (100) 13 (100) 13 (100) 
Steroid use for CRS, n (%) 29 (65.9) 7 (53.8) 22 (71.0) .31 
VariableOverall
N = 44
Low CMV IgG
N = 13
High CMV IgG
N = 31
P value
Age (y), median (range) at the time of CAR-T 64 (36-76) 63 (47-73) 64 (36-76) .32 
Sex, n (%)     
Female 15 (34.1) 5 (38.5) 10 (32.3) .74 
Male 29 (65.9) 8 (61.5) 21 (67.7)  
MM subtype, n (%)     
IgG 24 (54.5) 8 (61.5) 16 (51.6) 1.00 
IgA 8 (18.2) 2 (15.4) 6 (19.4)  
IgD 1 (2.3) 0 (0) 1 (3.2)  
Bence–Jones 11 (25.0) 3 (23.1) 8 (25.8)  
R2-ISS stage at CAR-T, n (%)     
Stage 1 6 (13.6)) 4 (30.8) 2 (6.5) .20 
Stage 2 14 (31.8) 3 (23.1) 11 (35.5)  
Stage 3 22 (50) 6 (46.2) 16 (51.6)  
Stage 4 1 (2.3) 0 (0) 1 (3.2)  
Unknown 1 (2.3) 0 (0) 1 (3.2)  
MyCARe, n (%)     
Low 12 (27.3) 5 (38.5) 7 (22.6) .49 
Intermediate 29 (65.9) 7 (53.8) 22 (71.0)  
High 3 (6.8) 1 (7.7) 2 (6.5)  
CMV IgG (AU/mL), median (range) 187.15 (20.6-250) 64.7 (20.6-113.2) 238.2 (115.6-250) <.001 
Previous treatment lines, median (range) 3 (2-10) 3 (2-6) 3 (2-10) .50 
Previous autologous stem cell transplantation, n (%) 26 (59.1) 9 (69.2) 17 (54.8) .51 
Extramedullary disease, n (%) 6 (14.3) 1 (7.7) 5 (17.2) .65 
Triple-class refractory, n (%) 33 (75.0) 12 (92.3) 21 (67.7) .13 
Penta refractory, n (%) 3 (6.8) 1 (7.7) 2 (6.5) 
High-risk cytogenetic abnormality until CAR-T therapy, n (%)     
High-risk 31 (72.1) 8 (61.5) 23 (74.2) .46 
del(17p) 13 (29.5) 3 (23.1) 10 (32.3) .72 
t(4;14) 9 (20.5) 2 (15.4) 7 (22.6) .70 
t(14;16) 1 (2.3) 1 (7.7) 0 (0) .21 
1q abnormality 28 (63.6) 7 (53.8) 21 (67.7) .30 
Tocilizumab use for CRS, n (%) 44 (100) 13 (100) 13 (100) 
Steroid use for CRS, n (%) 29 (65.9) 7 (53.8) 22 (71.0) .31 

MM, multiple myeloma; MyCARe, Myeloma CAR-T Relapse model; R2-ISS, Second Revision of the International Staging System.

Triple-class refractory is defined as refractory to proteasome inhibitors, immunomodulatory drugs, and anti-CD38 antibody.

Penta refractory is defined as refractory to 2 proteasome inhibitors, 2 immunomodulatory drugs, and anti-CD38 antibody.

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