Table 1.
Patient characteristics | Total (n = 72) |
---|---|
Age (years), median (IQR) | 61.5 (53.6, 70) |
Underlying disease: | |
Rheumatoid arthritis, n (%) | 30 (42.2) |
ANCA-associated vasculitis, n (%) | 18 (25.4) |
Connective tissue disease⁎, n (%) | 21 (29.6) |
IgG4-related disease, n (%) | 3 (4.2) |
Rituximab Schedule | |
Every 6 months, n (%) | 61 (85.9) |
Every 12 months, n (%) | 10 (14.2) |
Cumulative RTX (mg), median (IQR) | 7000 (4000, 11,000) |
Concomitant DMARD (any), n (%) | 39 (54.9) |
Mycophenolate mofetil, n (%) | 10 (14.1) |
Methotrexate, n (%) | 12 (16.9) |
Hydroxychloroquine, n (%) | 9 (12.7) |
Steroids (prednisone equivalent) | |
≥ 20 mg/day, n (%) | 2 (2.8) |
10-19 mg/day, n (%) | 5 (7) |
< 10 mg/day, n (%) | 31 (43.1) |
No steroids, n (%) | 34 (47.2) |
B cell counts: | |
Absolute CD19 count (#/uL), median (IQR): (n = 28) | 14.77 (8.38, 21.57) |
Absolute CD20 count (#/uL), median (IQR): (n = 28) | 9.02 (5.19, 14.67) |
History of hypogammaglobulinemia n, (%) (n = 41) | 20 (48.8) |
Immunoglobulin M hypogammaglobulinemia n, (%) (n = 41) | 17 (41.5) |
Immunoglobulin G hypogammaglobulinemia n, (%) (n = 41) | 10 (24.4) |
Immunoglobulin M (mg/dL), median (IQR) (n = 34) | 46 (19.5, 65) |
Immunoglobulin A, median (IQR) (n = 35) | 176 (100, 255) |
Immunoglobulin G, median (IQR) (n = 35) | 793 (665, 1048) |
Documented history of COVID-19 infection, n (%) | 7 (9.9) |
Influenza vaccine in 2020–2021 (yes/no) n (%) (n = 55) | 51 (92.7) |
Patient group according to provider preference for SARS-CoV-2 vaccine: | |
Universal recommendation for timing, n (%) | 41 (57.7) |
Individualized approach to timing, n (%) | 30 (42.2) |
Patient reported data on SARS-CoV-2 vaccine (n = 65) | |
Refused, n (%) | 0 (0) |
Planned, n (%) | 2 (3.1) |
Received, n (%) | 63 (95.4) |
Manufacturer of received vaccine (n = 63) | |
BNT162b2 mRNA, n (%) | 31 (49.2) |
mRNA-1273, n(%) | 26 (41.2) |
Ad26.COV2.SCovid-19, n(%) | 6 (9.5) |
Timing of SARS-CoV-2 vaccination post RTX (weeks), median (IQR) (n = 59) | 20.5 (13.3, 26) |
The connective tissue disease group is composed of systemic lupus erythematosus, inflammatory myopathies, anti-synthetase syndrome, overlap syndromes, and mixed connective tissue disease patients.