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  • Presentation

Recent Advances in Vitiligo and Melasma Treatment

Description

The talk reviewed major recent advances in pigmentary disorders, focusing first on vitiligo and then melasma. For vitiligo, it highlighted new understanding of disease biology, especially the role of CD8+ T cells, interferon gamma, and the JAK-STAT pathway, which has led to new therapies such as topical ruxolitinib, the first approved treatment for repigmentation in vitiligo. The speaker emphasized that responses may be slow and sometimes require long-term or combination treatment, including adding narrowband UVB phototherapy to improve outcomes. He also discussed emerging oral JAK inhibitors such as ritlecitinib, povorcitinib, upadacitinib, and baricitinib, as well as procedural options like autologous skin cell suspension transplantation for patients who do not respond to medical therapy. For melasma, the talk summarized expert consensus recommending topical therapy first, limiting hydroquinone use, and considering oral tranexamic acid if response is inadequate. It also reviewed newer non-hydroquinone topical options such as cysteamine, thiamidol, and 2-MNG, and noted reassuring safety data for tranexamic acid when appropriately screened. Overall, the presentation emphasized rapid progress in both vitiligo and melasma treatment, with expanding medical and procedural options.

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Conclusions

  • Vitiligo management is shifting toward a combination of topical JAK inhibition, phototherapy, systemic options, and surgery tailored to disease extent and activity.
  • Topical ruxolitinib is effective and generally well tolerated for vitiligo, with facial skin responding best but meaningful repigmentation also occurring at nonfacial sites.
  • A lack of meaningful improvement by 6 months does not necessarily mean treatment failure, because some patients continue to improve with longer ruxolitinib treatment.
  • Adding narrow-band UVB phototherapy can accelerate or enhance repigmentation when topical ruxolitinib alone is insufficient.
  • Multiple oral JAK inhibitors, including ritlecitinib, povorcitinib, and upadacitinib, show promising efficacy signals for vitiligo and may expand future treatment options.
  • Upadacitinib demonstrated significant efficacy versus placebo in phase 3 vitiligo trials with no major new safety concerns.
  • Autologous skin cell suspension transplantation appears to be an effective procedural option for stable, treatment-refractory vitiligo, often with strong repigmentation outcomes.
  • For melasma, first-line treatment remains topical therapy, with hydroquinone limited in duration and non-hydroquinone alternatives increasingly supported by evidence.
  • Oral tranexamic acid can be a useful adjunct for melasma in appropriately screened patients, and available data suggest low short-term thromboembolic risk.
  • Newer depigmenting agents such as cysteamine, thiamidol, and 2-MNG can provide efficacy comparable to hydroquinone with potentially better tolerability or as useful alternatives.
  • Combining topical agents with oral tranexamic acid and procedural approaches may improve melasma outcomes when faster or greater improvement is needed.
  • Overall, the field of pigmentary disorders has made substantial progress, with expanding evidence-based options for both repigmentation in vitiligo and depigmentation control in melasma.
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