What are the current treatment options for psoriasis?

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Last updated: December 2, 2025View editorial policy

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Current Treatment for Psoriasis

For mild psoriasis with limited body surface area, start with calcipotriene/betamethasone dipropionate combination topical therapy once daily for 4-8 weeks, which achieves clear or almost clear skin in 48-74% of patients; for moderate-to-severe disease or symptomatic psoriasis regardless of extent, initiate systemic therapy with biologics (IL-17, IL-23, or IL-12/23 inhibitors preferred over TNF inhibitors for superior skin efficacy) or phototherapy. 1, 2

Disease Severity Classification and Treatment Selection

Treatment intensity must be driven by symptoms and quality of life impact, not just body surface area percentage. 2

Mild psoriasis criteria:

  • Less than 5% body surface area involvement 3
  • Generally asymptomatic (no pain, bleeding, or itching) 3
  • Candidates for topical therapy alone 3

Moderate-to-severe psoriasis requires systemic or phototherapy if:

  • Symptomatic disease present 2, 3
  • More than minimal quality of life impact 3
  • Inadequate response to topical therapy 3
  • ≥5% body surface area involvement 2

First-Line Topical Therapy for Mild Psoriasis

Apply calcipotriene/betamethasone dipropionate combination product once daily for 4-8 weeks as the most effective topical approach. 2, 4

For trunk and extremities, use high-potency corticosteroids such as clobetasol propionate 0.05% or halobetasol propionate 0.05%. 2, 4

Site-specific modifications:

  • Facial/intertriginous areas: Use low-potency corticosteroids or calcitriol ointment to prevent skin atrophy 2, 4
  • Scalp: Use calcipotriene foam or calcipotriene plus betamethasone dipropionate gel for 4-12 weeks 3, 4
  • Nails: Apply calcipotriene combined with betamethasone dipropionate, though efficacy is limited due to poor nail matrix penetration 1, 3

Critical dosing limits:

  • Maximum vitamin D analogue use: 100 g per week to avoid hypercalcemia 2, 4

Maintenance Therapy Strategy

After achieving initial control, transition to weekend-only high-potency corticosteroid application with weekday vitamin D analogue therapy to minimize corticosteroid exposure while maintaining efficacy. 2

Specific regimen:

  • Apply high-potency topical corticosteroid twice daily on weekends only 2
  • Apply vitamin D analogue twice daily on weekdays 2

Combination Strategies to Enhance Efficacy

Combining tazarotene with medium- or high-potency corticosteroids for 8-16 weeks increases efficacy while reducing local adverse events and prolonging remission. 2, 4

When using systemic biologics, adding ultra-high potency topical corticosteroid for 12 weeks accelerates clearance and improves outcomes. 2, 4

Phototherapy for Moderate-to-Severe Psoriasis

Narrowband UVB phototherapy is first-line systemic treatment for patients with ≥5% body surface area or inadequate response to topicals. 2, 4

Additional phototherapy options include oral PUVA, bath PUVA with or without acitretin, and 308-nm excimer laser for localized resistant areas such as scalp and skin folds. 2, 3

Phototherapy is particularly efficacious for psoriasis affecting the trunk and extremities. 1

Traditional Systemic Agents for Moderate-to-Severe Psoriasis

Methotrexate:

  • Inhibits dihydrofolate reductase and increases endogenous adenosine with anti-inflammatory effects 2, 4
  • Requires regular monitoring of complete blood count, liver function tests, and serum creatinine 2, 4
  • FDA-approved since 1972 for psoriasis treatment 3

Cyclosporine:

  • Dose: 3-5 mg/kg/day in short 3-4 month "interventional" courses 2, 4
  • Particularly effective for erythrodermic psoriasis requiring rapid response 2
  • Requires monitoring of blood pressure, renal function, and lipid profile 4

Acitretin:

  • Decreases keratinocyte hyperproliferation and restores normal epidermal differentiation 2, 3
  • Conditionally recommended for psoriasis in patients with psoriatic arthritis due to limited efficacy as monotherapy for plaque psoriasis 1
  • Can be efficacious for pustular psoriasis 1
  • Cannot be used in women of childbearing potential due to teratogenicity 2, 3

Other oral therapies:

  • PDE4 inhibitors and JAK inhibitors are strongly recommended for widespread psoriasis or disease unresponsive to topicals 1

Biologic Therapies for Moderate-to-Severe Psoriasis

Biologics are an option for first-line treatment of moderate-to-severe plaque psoriasis due to their efficacy and acceptable safety profiles. 2

Efficacy hierarchy for skin involvement: Newer mode of action drugs (IL-17, IL-12/23, and IL-23 inhibitors) show higher efficacy for skin involvement than TNF inhibitors in head-to-head studies. 1

Strongly recommended biologic classes:

  • IL-23 inhibitors: Guselkumab, tildrakizumab, risankizumab, mirikizumab (newer generation with favorable efficacy profiles) 2
  • IL-17 inhibitors 1
  • IL-12/23 inhibitors 1
  • TNF inhibitors 1

FDA-approved TNF inhibitor example (Adalimumab/HUMIRA):

  • Indicated for moderate-to-severe chronic plaque psoriasis in adults who are candidates for systemic therapy or phototherapy when other systemic therapies are medically less appropriate 5
  • Dosing: 80 mg initial dose, followed by 40 mg every other week starting one week after initial dose 5
  • Black box warnings: Increased risk of serious infections (including tuberculosis, bacterial sepsis, invasive fungal infections) and malignancies (including lymphoma) 5
  • Perform test for latent TB before starting; if positive, treat TB prior to initiating therapy 5

Selection criteria between biologics:

  • Results of head-to-head studies in psoriasis populations 1
  • Presence of comorbidities 1
  • Disease activity in other psoriatic arthritis domains if applicable 1

Agents with limited evidence for skin disease:

  • Leflunomide and sulfasalazine (csDMARDs) have limited evidence for efficacy in cutaneous psoriasis 1
  • CTLA4-Ig (abatacept) has limited evidence for efficacy in skin disease 1

Critical Pitfalls to Avoid

Never combine salicylic acid with calcipotriene simultaneously—the acidic pH inactivates calcipotriene and eliminates its effectiveness. 2, 4

Avoid systemic corticosteroids in psoriasis as they cause disease flare during taper. 4

Do not use high-potency corticosteroids on face or flexures—use low-potency agents or tacrolimus instead to prevent skin atrophy. 2

Limit continuous high-potency corticosteroid use to prevent skin atrophy, striae, telangiectasia, and HPA axis suppression. 2, 4

Avoid IL-17 inhibitors (secukinumab and brodalumab) in patients with known Crohn's disease as they exacerbated disease in RCTs. 1

Drugs that worsen psoriasis:

  • Avoid or use with extreme caution: lithium, chloroquine, and mepacrine (may cause severe deterioration) 2
  • May precipitate or worsen psoriasis: beta-blockers, NSAIDs, and alcohol 2

Special Considerations for Comorbid Inflammatory Bowel Disease

For patients with concurrent Crohn's disease or ulcerative colitis, TNF inhibitors (excluding etanercept) and IL-12/23 inhibitors have demonstrated efficacy in high-quality RCTs. 1

Methotrexate shows efficacy in Crohn's disease and ulcerative colitis based on RCT data. 1

Etanercept did not show efficacy for inflammatory bowel disease. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Current Treatment Options for Psoriasis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Psoriasis Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Psoriasis Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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