Table 4.
Characteristic | Patients with AS (N = 78) |
---|---|
Duration of treatment with secukinumaba | |
Mean (SD), months | 4.7 (4.6) |
Median (IQR), months | 3.5 (1.0–6.0) |
Dose | |
Initial loading dose, n (%) | |
150 mg every weekb | 31 (39.7) |
300 mg every weekc | 42 (53.8) |
Otherd | 1 (1.3) |
No loading dose | 4 (5.1) |
Received maintenance dose, n (%) | |
Initial maintenance dosee | |
150 mg every 4 weeks | 41 (56.2) |
300 mg every 4 weeks | 32 (43.8) |
Current use of secukinumab, n (%) | |
Patient still receiving secukinumab | 74 (94.9) |
Patient discontinued secukinumab | 3 (3.8) |
Reason for secukinumab discontinuation, n (%)f | |
Lack/loss of efficacy/effectiveness | 2 (66.7) |
Patient request | 1 (33.3) |
Otherg | 1 (33.3) |
Unknown status of secukinumab use | 1 (1.3) |
AS ankylosing spondylitis, IQR interquartile range
aDuration of treatment with secukinumab was calculated among all patients; the calculated duration underestimates the true duration because most patients were still receiving secukinumab at the time of the survey
bAmong the 31 patients who initiated secukinumab at 150 mg every week, 24 received an initial maintenance dose of 150 mg every 4 weeks, five received 300 mg every 4 weeks, and two did not remain on the therapy long enough to receive maintenance treatment
cAmong the 42 patients who initiated secukinumab at 300 mg every week, 14 received an initial maintenance dose of 150 mg every 4 weeks, 26 received 300 mg every 4 weeks, and two did not remain on the therapy long enough to receive maintenance treatment
dOther initial loading dose included “methotrexate”
eThe proportions of initial maintenance doses were calculated among patients who received a maintenance dose
fThe proportions of reasons for discontinuation were calculated among patients who discontinued secukinumab. Multiple reasons could be selected for each patient
gOther reason included “patient deceased”