Table 3.

HRs and 95% CIs of the association of race and ethnicity with PFS and OS


Race and ethnicity
PFSOS 
Model 1 Model 2 Model 1 Model 2§ 
n (n event)HR (95% CI)HR (95% CI)n (n event)HR (95% CI)HR (95% CI)
Non-Hispanic White 129 (81) 1.00 (referent) 1.00 (referent) 129 (46) 1.00 (referent) 1.00 (referent) 
Hispanic 16 (11) 1.45 (0.77-2.73) 1.10 (0.53-2.30) 16 (6) 1.37 (0.58-3.23) 1.39 (0.54-3.63) 
Non-Hispanic Black 29 (19) 1.33 (0.81-2.21) 1.22 (0.72-2.08) 28 (10) 1.10 (0.55-2.17) 1.13 (0.54-2.38) 

Race and ethnicity
PFSOS 
Model 1 Model 2 Model 1 Model 2§ 
n (n event)HR (95% CI)HR (95% CI)n (n event)HR (95% CI)HR (95% CI)
Non-Hispanic White 129 (81) 1.00 (referent) 1.00 (referent) 129 (46) 1.00 (referent) 1.00 (referent) 
Hispanic 16 (11) 1.45 (0.77-2.73) 1.10 (0.53-2.30) 16 (6) 1.37 (0.58-3.23) 1.39 (0.54-3.63) 
Non-Hispanic Black 29 (19) 1.33 (0.81-2.21) 1.22 (0.72-2.08) 28 (10) 1.10 (0.55-2.17) 1.13 (0.54-2.38) 

N = 174.

BCMA, B-cell maturation antigen; ECOG, Eastern Cooperative Oncology Group.

One patient had missing date of death and excluded from models of OS.

Model 1 is unadjusted.

Model 2 includes prior BCMA therapy, high-risk cytogenetics, extramedullary disease, cell dose, ECOG at lymphodepletion chemotherapy, penta-refractory status, age, number of prior lines of therapy, sex, baseline ferritin, and baseline CRP.

§

Model 2 includes prior BCMA therapy, extramedullary disease, cell dose, ECOG at lymphodepletion chemotherapy, penta-refractory status, age, number of prior lines of therapy, and baseline ferritin. High-risk cytogenetics is included as a strata term.

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