Table 5.
Characteristic | Patients with PsA (N = 153) |
---|---|
Duration of treatment with secukinumab, mean (SD), monthsa | 5.9 (4.6) |
Dose | |
Received loading regimen, n (%) | 144 (94.1) |
150 mg every weekb | 50 (32.7) |
300 mg every weekc | 94 (61.4) |
No loading regimen | 9 (5.9) |
Received maintenance dose, n (%) | 145 (94.8) |
Initial maintenance dosed | |
150 mg every 4 weeks | 72 (49.7) |
300 mg every 4 weeks | 73 (50.3) |
Current secukinumab use, n (%) | |
Still receiving secukinumab | 138 (90.2) |
Discontinued secukinumab | 9 (5.9) |
Reason for secukinumab discontinuation, n (%)e | |
Lack/loss of efficacy/effectiveness | 5 (55.6) |
Intolerance to the treatment | 2 (22.2) |
Adverse events from the treatment | 2 (22.2) |
Worsening or new comorbid condition | 1 (11.1) |
Unknown secukinumab treatment status | 6 (3.9) |
PsA psoriatic arthritis; SD standard deviation
aDuration of treatment with secukinumab was calculated among all patients; the calculated duration may underestimate the true duration because most patients were still receiving secukinumab at the time of chart abstraction
bAmong the 50 patients who initiated secukinumab at 150 mg every week, 43 received an initial maintenance dose of 150 mg every 4 weeks, 6 received 300 mg every 4 weeks, and 1 did not receive maintenance treatment
cAmong the 94 patients who initiated secukinumab at 300 mg every week, 25 received an initial maintenance dose of 150 mg every 4 weeks, 63 received 300 mg every 4 weeks, 2 did not receive maintenance treatment, and 4 did not remain on the therapy long enough to receive maintenance treatment
dThe proportions of initial maintenance doses were calculated among patients who received a maintenance dose
eThe proportions of reasons for discontinuation were calculated among patients who discontinued secukinumab. Multiple reasons could be selected for each patient