Excimer 308 nm in Vitiligo: Focal Therapy for Face/Neck and Acral Margins

Key Takeaways

  • Targeted 308 nm is effective for limited facial/neck lesions and expanding edges of patches.
  • Acral sites (hands/feet) respond slower; pairing with tacrolimus/pimecrolimus improves odds.
  • Typical schedule: 2–3×/week, 20–30 sessions initial; visible perifollicular islands by weeks 4–8.
  • Adverse events are mostly grade 1–2 erythema; careful dose titration minimizes burns.

Abstract

Excimer 308 nm provides high-fluence, small-field UVB for focal vitiligo. Evidence from RCTs and cohorts supports superiority over placebo/observation for facial lesions and utility as an adjunct for acral margins. We summarize practical dosing, targeting strategies, site-specific outcomes, combinations with calcineurin inhibitors, and safety.

Protocols & Dosing

Table 1. Typical 308 nm dosing frameworks.
Parameter Typical setting Notes
Frequency 2–3 sessions/week ≥48 h between sessions
Start dose 150–300 mJ/cm² Phototype & site adjusted
Increment 10–25% per treatment Hold if erythema >24 h
Course length 20–30 sessions (initial) Extend if improving to 40–50
Field size 2–5 cm spot/handpiece Feather at borders to blend

Clinical Indications & Targeting

  • Focal/segmental lesions on face/neck or cosmetically sensitive zones.
  • Advancing edges of nonsegmental patches; perilesional halos.
  • Acral margins where cabinet NB-UVB underperforms.

Efficacy by Anatomic Site

Table 2. Response patterns (typical).
Site Response Notes
Face/neck High Early islands, rapid F-VASI gains
Trunk Moderate Better at edges than center
Acral Low–moderate Improves with tacrolimus/pimecrolimus

Combination with Topicals

  • Tacrolimus 0.1% / Pimecrolimus 1% applied between sessions increases response on face/neck and acral margins.
  • Sequence: treat with excimer → apply topical later the same day to reduce irritation.
  • Use with NB-UVB cabinet for widespread disease; excimer for resistant foci.

Safety

Table 3. Common adverse events.
Event Pattern Management
Erythema/tenderness Mild, dose-related Hold/reduce dose; emollients
Blistering (rare) Over-titration Immediate rest; lower restart
Hyperpigmentation Transient Feather borders; adjust spacing

Outcome Tables (framework)

Table 4. Study outcomes (fill with numerics).
Outcome Excimer Comparator Interpretation
F-VASI % change (face, 12–24 wks) Vehicle/observation Favours excimer
Responder rate (F-VASI50/75) Higher on face/neck
Acral response Improves with calcineurin inhibitor

Limitations

Small RCTs and heterogeneous protocols; durability data limited; access and operator technique influence outcomes.

References

  1. Randomized and cohort studies of 308 nm excimer in facial and acral vitiligo.
  2. Combination studies with tacrolimus/pimecrolimus and cabinet NB-UVB.
  3. Guidelines on targeted phototherapy dosing and safety.
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