Table 1.
Continuous Covariates | Units | Median (Range) |
---|---|---|
Body weight | kg | 79.0 (43.0‐130) |
BMI | kg/m2 | 28.1 (18.4‐37.0) |
Age | y | 53.0 (18.0‐75.0) |
Albumin | g/L | 45.0 (37.0‐54.0) |
ALT | U/L | 19.0 (7.00‐117) |
Bilirubin | μmol/L | 7.00 (1.50‐35.0) |
sST2 | ng/mL | 11.7 (1.56‐222) |
eGFR | mL/min/1.73 m2 | 87.9 (29.3‐161) |
Eosinophils | cells/μL | 180 (5.00‐1930) |
Categorical covariates | N (%) | |
Dose | ||
70 mg every 4 wks | 124 (33.7) | |
210 mg every 4 wks | 124 (33.7) | |
490 mg every 4 wks | 120 (32.6) | |
Sex | ||
Male | 122 (33.2) | |
Female | 246 (66.8) | |
Race | ||
Asian | 17 (4.6) | |
Black | 20 (5.4) | |
Native American | 17 (4.6) | |
Multiple | 5 (1.4) | |
White | 309 (84.0) | |
Subject‐level ADA status a | ||
Negative | 341 (92.7) | |
Positive | 27 (7.3) |
ADA, antidrug antibody; ALT, alanine aminotransferase; BMI, body mass index; eGFR, estimated glomerular filtration rate; PK, pharmacokinetic; sST2, soluble ST2; wks, weeks.
Patients are considered to be ADA positive if they had either treatment‐induced ADA or treatment‐enhanced ADA; otherwise, they were considered to be ADA negative.