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. 2021 Aug 3;9(8):950. doi: 10.3390/biomedicines9080950

Table A1.

Treatments mainly acting on immune dysreactivity and inflammatory response.

Treatment Posology Notes
Topical treatments
Topical Corticosteroids
- Clobetasol Propionate 0.05% Ointment or Cream
- Mometasone Furoate 0.1% Ointment or Cream
Once or twice a day for 12 weeks - first line treatment in the active phase
- anti-inflammatory and immunosuppressive activity
- effectiveness on both symptoms and objective features
- tachyphylaxis and dose-dependent side effects may be avoided by tapering regimens
- ointment formulation seems to be more effective in comparison with cream
- intralesional corticosteroid injection in recalcitrant forms
- long-term maintenance treatment (reactive, continuative or proactive regimens)
Topical Calcineurin Inhibitors
- Tacrolimus 0.1% Ointment
- Pimecrolimus 1% Cream
Twice a day for 8 to 24 weeks - second-line choice with lower effectiveness than ultra-potent corticosteroid
- immunosuppressive activity
- effectiveness on both symptoms and objective features
- possible transient burning sensation during the first weeks of treatment
Calcipotriol 0.005% Ointment Once to twice a day for 16 weeks - inhibition of inflammatory response
- attenuation of abnormal keratinocyte proliferation and differentiation
- effectiveness on symptoms
- alternative to standard treatment (weak evidence)
Oxatomide 5% gel Twice a day for periods of 14-days - antihistamine and anti-inflammatory properties
- effectiveness on both symptoms and objective features
- alternative to standard treatment (weak evidence)
Human Fibroblast Lysate Cream Twice daily for 12 weeks - presence of anti-inflammatory cytokines and wound-healing grow factors
- no more effective than placebo
Systemic treatments
Oral Cyclosporine 3–4 mg/kg/day for 12 weeks - immunosuppressive effect
- regression of symptoms and improvement of clinical features in resistant case
- weak evidence
Oral or Subcutaneous Metothrexate 10 to 15 mg/week - immunosuppressive effect
- regression of symptoms and improvement of clinical features in resistant case
- weak evidence
Baricitinib - inhibition of JAK 1/2
- anecdotal reports