Table 1.
Age (years)/sex | Disease treated | Vitiligo disease activity | Treatment regimen | TNF‐α antagonist dosing | Results | Report type | References |
---|---|---|---|---|---|---|---|
15–38/5 M, 1 F | Vitiligo | Progressive | Untreated for ≥ 3 months, then ETA (n = 2), IFX (n = 2), ADA (n = 2) | IFX: 5 mg kg−1 IV at weeks 0, 2, 6, then q8 wk. ETA: 50 mg SC 2 ×/wk. ADA: 80 mg SC at week 0, 40 mg SC at week 1, then 40 mg SC q2 wk | One worsened, five stabilized | PS | 71 |
24–34/4 M | Vitiligo | Progressive | Untreated for 2 months, then ETA | 50 mg SC 1 ×/wk for 12 weeks, then 25 mg 1 ×/wk for 4 weeks | Stabilized | PS | 74 |
42/F, 46/F | Vitiligo | Progressive | Continued NB‐UVB and topical calcineurin inhibitors, added ETA | 50 mg 2 ×/wk, then 50 mg 1 ×/wk for ≥ 1 year | Disease stabilization and repigmentation | PS | 64 |
M, male; F, female; ETA, etanercept; IFX, infliximab; ADA, adalimumab; NB‐UVB, narrowband ultraviolet B; IV, intravenously; SC, subcutaneously; PS, pilot study; q2 wk, every 2 weeks; 2 ×/wk, two times per week.