Table II.
Characteristics | Total |
---|---|
N = 2603 | |
Current systemic treatment at enrollment,∗n (%) | N = 2603 |
Dupilumab | 1914 (73.5%) |
Upadacitinib | 218 (8.4%) |
Tralokinumab-ldrm | 147 (5.6%) |
Methotrexate | 101 (3.9%) |
Cyclosporine | 21 (0.8%) |
Apremilast | 16 (0.6%) |
Abrocitinib | 13 (0.5%) |
Mycophenolate mofetil/mycophenolic acid | 8 (0.3%) |
Omalizumab | 5 (0.2%) |
Tofacitinib | 2 (0.1%) |
Tacrolimus | 1 (0.0%) |
Other treatment at enrollment,†n (%) | N = 2603 |
Corticosteroids | 83 (3.2%) |
Phototherapy | 62 (2.4%) |
Topical therapy | 1875 (72.0%) |
History of treatment at enrollment,‡n (%) | N = 2603 |
Systemic therapy§ | 1229 (47.2%) |
Corticosteroids | 498 (19.1%) |
Phototherapy | 326 (12.5%) |
Superpotent topical steroids, topical calcineurin inhibitors, or crisaborole | 2257 (86.7%) |
Number of systemic therapies§ before enrollment (excluding current therapy), n (%) | N = 2603 |
0 | 2356 (90.5%) |
1 | 199 (7.6%) |
2+ | 48 (1.8%) |
Frequencies may not sum to total as patients may be treated with multiple systemic therapies concomitantly.
Not mutually exclusive. Includes both treatment in use and treatment newly started/prescribed at enrollment.
Not mutually exclusive. Includes treatment started any time before enrollment, regardless of whether treatment is in use at enrollment.
Systemic therapy includes registry eligible biologics (tralokinumab-ldrm, dupilumab, secukinumab, ustekinumab, risankizumab-rzaa, ixekizumab, and omalizumab), eligible small molecules (abrocitinib, upadacitnib, baricitinib, apremilast, and tofacitinib), and eligible nonbiologic systemics (azathioprine, cyclosporine, methotrexate, mycophenolate mofetil, mycophenolic acid, and tacrolimus).