Table 1.

CART-BCMA cohort patient characteristics

CharacteristicRMP (n = 24)Non-RMP (n = 116)P value
Patient age, median (IQR), y 62 (57-66) 66 (61-70) .02 
Male 11 (46) 68 (59) .36 
Product infused    
cilta-cel 13 (54) 58 (50) .81 
ide-cel 11 (46) 58 (50)  
Out-of-specification products 1 (4.2) 5 (4.3) .99 
R-ISS at diagnosis >1 17/20 (85) 58/77 (75) .54 
Median previous lines of therapy (IQR) 5 (5-7) 6 (5-8) .04 
Previous autologous SCT 22 (92) 100 (86) .69 
Previous allogeneic SCT 0 (0) 5 (4.3) .67 
Triple-class refractory  19 (79) 96 (83) .90 
Penta-refractory disease  5 (21) 39 (34) .31 
ECOG at infusion <2 22 (92) 86 (74) .11 
High-risk cytogenetics at diagnosis  7/17 (41) 42/105 (40) .99 
Extramedullary disease 7 (29) 25 (22) .42 
Bridging therapy 23 (96) 109 (94) .99 
Lymphodepletion    
Flu/Cy 23 (96) 100 (87) .53 
Cy-based 1 (4) 13 (11)  
Bendamustine 1 (0.9)  
M-spike at CART, median (IQR), g/dL 0.9 (0-1.7) 0.25 (0-1.3) .15 
Differential light chain at CART, median (IQR), mg/L 245 (35-661) 91 (20-425) .20 
CharacteristicRMP (n = 24)Non-RMP (n = 116)P value
Patient age, median (IQR), y 62 (57-66) 66 (61-70) .02 
Male 11 (46) 68 (59) .36 
Product infused    
cilta-cel 13 (54) 58 (50) .81 
ide-cel 11 (46) 58 (50)  
Out-of-specification products 1 (4.2) 5 (4.3) .99 
R-ISS at diagnosis >1 17/20 (85) 58/77 (75) .54 
Median previous lines of therapy (IQR) 5 (5-7) 6 (5-8) .04 
Previous autologous SCT 22 (92) 100 (86) .69 
Previous allogeneic SCT 0 (0) 5 (4.3) .67 
Triple-class refractory  19 (79) 96 (83) .90 
Penta-refractory disease  5 (21) 39 (34) .31 
ECOG at infusion <2 22 (92) 86 (74) .11 
High-risk cytogenetics at diagnosis  7/17 (41) 42/105 (40) .99 
Extramedullary disease 7 (29) 25 (22) .42 
Bridging therapy 23 (96) 109 (94) .99 
Lymphodepletion    
Flu/Cy 23 (96) 100 (87) .53 
Cy-based 1 (4) 13 (11)  
Bendamustine 1 (0.9)  
M-spike at CART, median (IQR), g/dL 0.9 (0-1.7) 0.25 (0-1.3) .15 
Differential light chain at CART, median (IQR), mg/L 245 (35-661) 91 (20-425) .20 

Data are presented as n (%) unless otherwise specified. Bold values are statistically significant (P < .05).

Cy, cyclophosphamide; ECOG, Eastern Cooperative Oncology Group; Flu, fludarabine; R-ISS, Revised International Staging System; SCT, stem cell transplantation.

Triple-class–refractory disease was defined as disease refractory to an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody.

Penta-refractory disease was defined as a disease refractory to lenalidomide, pomalidomide, bortezomib, carfilzomib, and daratumumab.

High-risk cytogenetic abnormalities included del(17p), t(4;14), t(14;20), t(14;16), and gain/amplification of 1q.

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