Interval prolongation (n=27) | Continuation (n=27) | |||
Baseline | Week 28 | Baseline | Week 28 | |
Demographics | ||||
Age, mean±SD years | 60 ± 10 | – | 58 ± 13 | – |
Female, n (%) | 25 (93) | – | 26 (96) | – |
BMI, mean±SD | 24.8 ± 5.0 | – | 23.8 ± 4.3 | – |
Previous therapies | ||||
Prior DMARDs, median (IQR) | 3 (2–3) | – | 2 (2–3) | – |
Prior biologic, n (%) | 4 (15) | – | 3 (11) | – |
Adalimumab treatment, median (IQR) years | 6.0 (2.9–8.0) | – | 5.5 (1.8–8.3) | – |
Concomitant therapies | ||||
MTX use, n (%) | 26 (96) | 25 (93) | 25 (93) | 25 (93) |
MTX dosage, median (IQR) mg/week | 20 (15–21) | 15 (11–20) | 15 (10–20) | 15 (10–20) |
Prednisone use, n (%) | 4 (15) | 4 (15) | 1 (4) | 0 (0) |
Disease status | ||||
Disease duration, median (IQR) years | 11 (8–18) | – | 11 (6–19) | – |
ACPA positive, n (%) | 18 (67) | – | 21 (78) | – |
IgM-RF positive, n (%) | 20 (74) | – | 20 (74) | – |
Erosive disease, n (%) | 17 (63) | – | 17 (63) | – |
Primary outcome: DAS28-ESR, mean±SD | 2.0 ± 0.8 | 1.9 ± 0.7 | 1.6 ± 0.7 | 2.0 ± 0.9 |
Patient’s pain, median (IQR) mm | 15 (3–38) | 17 (4–34) | 10 (6–21) | 13 (9–22) |
Patient’s global, median (IQR) mm | 15 (3–37) | 16 (4–37) | 15 (11–25) | 19 (8–35) |
Physician’s global, median (IQR) mm | 4 (3–14) | 9 (2–21) | 12 (5–17) | 15 (7–26) |
Swollen joint count, median (IQR) | 0 (0–0) | 0 (0–0) | 0 (0–0) | 0 (0–0) |
Tender joint count, median (IQR) | 0 (0–0) | 0 (0–0) | 0 (0–0) | 0 (0–0) |
ESR, median (IQR) mm/hour | 9 (5–18) | 7 (5–18) | 5 (3–11) | 7 (4–14) |
CRP, median (IQR) mg/L | 1 (1–3) | 1 (1–2) | 1 (1–3) | 1 (1–2) |
HAQ, median (IQR) | 0.4 (0.1–1.0) | 0.5 (0.1–0.8) | 0.5 (0.1–1.3) | 0.6 (0.1–1.1) |
ACPA, anticitrullinated protein antibody; BMI, body mass index; CRP, C-reactive protein; DAS28, 28 joints disease activity score; DMARDs, disease-modifying anti-rheumatic drugs; ESR, erythrocyte sedimentation rate; HAQ, Health Assessment Questionnaire; IgM-RF, IgM rheumatoid factor; MTX, methotrexate; SD, standard deviation.