Tacrolimus 0.1% in Vitiligo: Efficacy by Anatomic Zone in Children and Adults

Key Takeaways

  • Face/neck consistently show the best repigmentation with tacrolimus 0.1%; early perifollicular islands predict response.
  • Acral (hands/feet) and longstanding lesions are comparatively refractory; consider adjunct NB-UVB or excimer 308 nm.
  • Useful as a steroid-sparing first-line agent on cosmetically sensitive skin (eyelids, periocular/perioral, genital).
  • Favorable safety for adults and children; most AEs are mild/transient burning or erythema without atrophy.

Abstract

Topical tacrolimus 0.1% is an established steroid-sparing therapy for vitiligo, with strongest efficacy on face and neck. This article synthesizes zone-specific outcomes, dosing practices, pediatric data, combination with light therapy, and safety signals.

Evidence by Anatomic Zone

Table 1. Typical response gradient by site.
Zone Response Notes
Face/neck High Early perifollicular islands; good F-VASI change
Trunk/limbs (non-acral) Moderate Slower than face; add NB-UVB if plateau
Acral (hands/feet) Low Combine with excimer or surgery when stable

Dosing & Practical Use

Table 2. Suggested regimen.
Aspect Recommendation Comment
Frequency BID thin layer to lesions Reduce to QD if irritation
Sequence After emollient; after light on treatment days Limits stinging
Duration Assess at 8–12 weeks; continue if improving Maintenance taper when plateau

Pediatric Considerations

  • Preferred on eyelids/periorificial areas to avoid steroid atrophy.
  • Adherence and gentle skincare (emollients, sun protection) enhance tolerability.
  • Monitor for transient burning; step-down to QD or alternate-day as needed.

Combination Strategies

  • NB-UVB 311 nm (2–3×/week) accelerates and deepens response versus monotherapy.
  • Excimer 308 nm for focal, resistant edges or acral margins.
  • Consider maintenance with tacrolimus after successful phototherapy to reduce relapse.

Safety

Table 3. Common adverse effects.
Event Pattern Management
Burning/tingling Mild, transient at initiation QD for 1–2 weeks; emollients
Erythema/irritation Occasional Brief pause; re-titrate
Folliculitis Rare Spacing doses; short rest

No cutaneous atrophy/telangiectasia expected with calcineurin inhibitors; suitable for long-term use on face/neck.

Outcome Tables (framework)

Table 4. Efficacy readouts to populate from studies.
Outcome Tacrolimus 0.1% Comparator Interpretation
F-VASI % change (12–24 wks) Vehicle/observation Favours tacrolimus on face/neck
F-VASI50/75 responders Higher proportion on face
Acral response Limited; needs combination

Limitations

Heterogeneous endpoints and small RCTs/split-face designs; limited long-term off-drug durability data; acral outcomes remain suboptimal.

References

  1. Split-face/RCT evidence for tacrolimus 0.1% in facial/periorificial vitiligo.
  2. Cohort and pediatric series detailing zone-specific responses and safety.
  3. Combination studies with NB-UVB and excimer for refractory sites.
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