Overall n = 35 | Baricitinib n = 15 | Tofacitinib n = 10 | Upadacitinib n = 10 | |
---|---|---|---|---|
Age, years mean ± SD | 72.3 ± 8.0 | 75.6 ± 7.6 | 67.6 ± 6.3 | 73.0 ± 8.2 |
Sex, female/male n (% female) | 30/5 (85.7) | 14/1 (93.3) | 10/0 (100) | 6/4 (60) |
Time from GCA diagnosis to JAKi initiation (months), median [IQR] | 30 [12–48] | 32 [12–48] | 12 [10.2–45.0] | 39 [22.5–75.0] |
CLASSIFICATION/DIAGNOSTIC CRITERIA | ||||
Criteria used in the GiACTA trial, n (%) | 28 (80) | 13 (87) | 8 (80) | 7 (70) |
ACR 1990, n (%) | 21 (60) | 7 (47) | 6 (60) | 8 (80) |
GCA PHENOTYPE | ||||
Cranial GCA | 15 (43) | 6 (17) | 4 (40) | 5 (50) |
Extracranial GCA | 7 (20) | 3 (9) | 2 (20) | 2 (20) |
Mixed GCA | 13 (37) | 6 (17) | 4 (40) | 3 (30) |
POSITIVE TEMPORAL ARTERY BIOPSY, n (%) | 15/24 (62) | 6/10 (60) | 4/7 (57) | 5/7 (71) |
POSITIVE IMAGING TECHNIQUE, n (%) | 24 (69) | 11 (73) | 6 (60) | 7 (70) |
Ultrasonography, n positive/n performed (% positive) | 7/15 (47) | 4/9 (44) | 1/2 (50) | 2/4 (50) |
Positron emission tomography, n positive/n performed (% positive) | 16/22 (73) | 7/9 (78) | 6/7 (86) | 3/6 (50) |
Magnetic resonance-angiography, n positive/n performed (% positive) | 3/9 (33) | 1/2 (50) | 1/3 (33) | 1/4 (25) |
Computed tomography-angiography, n positive/n performed (% positive) | 4/13 (31) | 1/3 (33) | 1/2 (50) | 2/8 (25) |
CARDIOVASCULAR RISK FACTORS | ||||
High blood pressure, n (%) | 26 (74) | 11 (73) | 6 (60) | 9 (90) |
Dyslipidemia, n (%) | 16 (46) | 9 (60) | 2 (20) | 5 (50) |
Diabetes, n (%) | 9 (26) | 4 (27) | 3 (30) | 2 (20) |
Previous or current smoking history, n (%) | 8 (23) | 4 (27) | 0 (0) | 4 (40) |
SYSTEMIC MANIFESTATIONS | ||||
PMR, n (%) | 12 (34) | 4 (27) | 4 (40) | 4 (40) |
Constitutional syndrome, n (%) | 10 (29) | 7 (47) | 2 (20) | 1 (10) |
Asthenia, n (%) | 16 (46) | 8 (23) | 5 (50) | 3 (30) |
CRANIAL AND ISCHEMIC MANIFESTATIONS | ||||
Headache, n (%) | 15 (43) | 7 (47) | 5 (50) | 3 (30) |
Jaw claudication, n (%) | 6 (17) | 1 (7) | 2 (20) | 3 (30) |
Visual symptoms, n (%) | 5 (14) | 3 (20) | 1 (10) | 1 (10) |
Stroke, n (%) | 2 (6) | 1 (7) | 1 (0) | 0 (0) |
LARGE-VESSEL INVOLVEMENT | 20 (57) | 10 (67) | 6 (60) | 4 (40) |
LABORATORY | ||||
ESR, mm/1st hour, median [IQR] | 28 [7–48] | 39 [10.5–60.5] | 34 [28–48] | 7 [2–10] |
CRP, mg/dL, median [IQR] | 0.9 [0.4–2.5] | 1 [0.4–3.5] | 0.9 [0.6-2] | 0.7 [0.3–1.8] |
Hb, g/dL, mean ± SD | 12.7 ± 1.7 | 12.4 ± 1.7 | 12.5 ± 1.4 | 13.6 ± 2.0 |
Previous synthetic conventional immunosuppressants use, n (%) | ||||
Methotrexate, n (%) | 22 (63) | 9 (60) | 7 (70) | 6 (60) |
Leflunomide, n (%) | 1 (3) | 0 (0) | 1 (10) | 0 (0) |
Antimalarials, n (%) | 3 (9) | 0 (0) | 2 (20) | 1 (10) |
Previous biologic immunosuppressants use, n (%) | ||||
Tocilizumab, n (%) | 26 (74) | 8 (53) | 9 (90) | 9 (90) |
Sarilumab, n (%) | 3 (9) | 2 (13) | 0 (0) | 1 (10) |
Adalimumab, n (%) | 2 (6) | 1 (7) | 0 (0) | 1 (10) |
Abatacept, n (%) | 8 (23) | 2 (13) | 4 (40) | 2 (20) |
Ustekinumab, n (%) | 2 (6) | 0 (0) | 1 (10) | 1 (10) |
GLUCOCORTICOIDS AT JAKi INITIATION | ||||
Patients on prednisone, n (%) | 32 (91) | 14 (93) | 10 (100) | 8 (80) |
Prednisone dose, mg/day, median [IQR] | 16.2 [8.7–30] | 10 [6.2–22.5] | 20 [16.2–30] | 13.1 [5.6–22.5] |