Treatment Options for Psoriasis
For psoriasis treatment, biologic therapy targeting IL-17 or IL-23 pathways is the most effective approach for moderate-to-severe disease, while combination therapy with potent corticosteroids and vitamin D analogs is recommended for mild psoriasis. 1
Disease Classification and Treatment Selection
Psoriasis severity is classified based on body surface area (BSA) involvement:
- Mild disease: <10% BSA
- Moderate-to-severe disease: ≥10% BSA or significant impact on quality of life 1
Treatment selection follows this algorithm:
Mild Psoriasis (<10% BSA)
First-line: Topical Therapy
Combination therapy: Potent corticosteroid + vitamin D analog (calcipotriene/calcipotriol)
- Provides synergistic effects
- Reduces corticosteroid-related side effects
- Extends treatment benefit and remission
- Maximum 100g of vitamin D analogs weekly (to avoid hypercalcemia) 1
Topical corticosteroids by potency class:
Alternative topicals:
- Tazarotene: Efficacy comparable to mid-potency corticosteroids (contraindicated in pregnancy) 1
- Calcineurin inhibitors (tacrolimus, pimecrolimus): Particularly effective for facial and intertriginous psoriasis with no risk of skin atrophy 1
- For scalp psoriasis: Medicated shampoos with coal tar, salicylic acid, or solutions/foams of corticosteroids/vitamin D analogs 1
If inadequate response to topicals: Phototherapy
- Narrowband UVB (first-line phototherapy option)
- Targeted phototherapy with 308-nm excimer laser for localized lesions
- PUVA (psoralen plus UVA) if narrowband UVB is inadequate 1
Moderate-to-Severe Psoriasis (≥10% BSA)
First-line: Biologic Therapy
- IL-17 inhibitors: Highest efficacy for skin involvement, strongly recommended for skin and nail psoriasis 1
- IL-23 inhibitors: Excellent efficacy and safety profiles, strongly recommended for skin and nail disease 1
- TNF-α inhibitors (e.g., adalimumab): Particularly effective when psoriatic arthritis is present 1, 2
- IL-12/23 inhibitors: Effective for both skin and joint manifestations 1
Alternative Systemic Therapies
- JAK inhibitors: Oral agents that block multiple cytokine pathways 1
- PDE4 inhibitors (e.g., apremilast): Moderate efficacy but favorable safety profile 1
- Traditional systemics:
- Methotrexate: 10-15 mg weekly starting dose, requires monitoring of CBC, liver function, and renal function 1
- Cyclosporine: Rapid control but limited to short-term use due to nephrotoxicity 1
- Acitretin: Less effective as monotherapy, more effective for pustular variants, contraindicated in women of childbearing potential 1
Monitoring and Maintenance
Evaluate treatment response after 4 weeks for topical therapy 1
Monitor for adverse effects:
Proactive maintenance therapy after achieving control:
- Use combination products or separate products with corticosteroid in morning and vitamin D analog in evening 1
Special Populations
- Pediatric patients: Use lower potency corticosteroids 1
- Psoriatic arthritis: Early treatment to prevent joint damage
- Mild disease: NSAIDs
- Moderate disease: DMARDs
- Moderate-severe disease: TNF inhibitors 1
Treatment Pitfalls to Avoid
- Overuse of potent corticosteroids: Limit to 4 weeks to prevent skin atrophy
- Inadequate monitoring of systemic therapies (especially methotrexate and biologics)
- Failure to screen for TB before starting TNF blockers like adalimumab 2
- Ignoring comorbidities when selecting therapy (e.g., psoriatic arthritis presence should guide toward TNF inhibitors)
- Not considering maintenance therapy after achieving disease control
The American Academy of Dermatology's treatment approach represents the most current evidence-based guidance, emphasizing the importance of matching treatment intensity to disease severity while considering safety profiles and patient-specific factors.