Treatment Options for Psoriasis
For psoriasis treatment, biologics targeting IL-17 or IL-23 pathways are the most effective options for moderate-to-severe disease, while combination therapy with potent corticosteroids and vitamin D analogs is recommended for mild disease. 1
Disease Classification and Treatment Approach
Psoriasis treatment is guided by disease severity:
- Mild disease (<10% body surface area [BSA])
- Moderate-to-severe disease (≥10% BSA or significant impact on quality of life) 1
First-Line Treatment Options
For Mild Psoriasis (< 10% BSA):
- Topical Therapy:
First choice: Combination of potent corticosteroid with vitamin D analog (calcipotriene/calcipotriol) 1
- Provides synergistic effects
- Reduces corticosteroid-related side effects
- Extends treatment benefit and remission
- Maximum 100g of vitamin D analogs weekly to avoid hypercalcemia
Topical corticosteroid options by potency class:
- Class 1 (Ultrahigh-potency): Clobetasol propionate, Halobetasol propionate
- Class 2-5 (High to moderate potency): Betamethasone dipropionate, Triamcinolone acetonide
- Class 6-7 (Low potency): Hydrocortisone, Desonide 1
Other topical options:
For Moderate-to-Severe Psoriasis (≥10% BSA):
Biologic Therapy (first-line for moderate-to-severe disease):
- IL-17 inhibitors - higher efficacy for skin involvement than TNF inhibitors 1
- IL-23 inhibitors - excellent efficacy and safety profiles 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
Phototherapy:
Systemic Oral Agents:
- Methotrexate - 10-15 mg weekly starting dose, requires monitoring of CBC, liver function, and renal function 1
- Cyclosporine - rapid control of severe psoriasis but limited to short-term use due to nephrotoxicity 1
- Acitretin - oral retinoid, more effective for pustular psoriasis variants, contraindicated in women of childbearing potential 1
- JAK inhibitors - oral agents blocking multiple cytokine pathways 1
- PDE4 inhibitors (apremilast) - moderate efficacy with favorable safety profile 1
Specific Biologic Treatment Details
For moderate-to-severe plaque psoriasis, adalimumab (Humira) is administered as follows:
- Initial dose: 80 mg
- Maintenance: 40 mg every other week starting one week after initial dose 2
Important safety considerations for biologics:
- Increased risk of serious infections including tuberculosis
- Risk of malignancy, including lymphoma
- Requires TB testing before initiation 2
Special Populations
- Pediatric patients: Use lower potency corticosteroids 1
- Psoriatic arthritis: Early treatment recommended to prevent joint damage
- NSAIDs for mild disease
- DMARDs for moderate disease
- TNF inhibitors for moderate-severe disease 1
Treatment Monitoring
- Evaluate response after 4 weeks for topical therapy
- Limit potent corticosteroid use to 4 weeks to minimize skin atrophy risk
- Regular monitoring for adverse effects:
- Corticosteroids: skin atrophy, telangiectasia, striae
- Methotrexate: hepatotoxicity, bone marrow suppression
- Biologics: infections, injection site reactions 1
Maintenance Therapy
Proactive maintenance therapy after achieving disease control is recommended to prevent relapses, using combination products or separate products with corticosteroid in the morning and vitamin D analog in the evening 1
Treatment Algorithm
- Assess disease severity (BSA and impact on quality of life)
- For mild disease: Start with topical combination therapy (corticosteroid + vitamin D analog)
- For moderate-to-severe disease or inadequate response to topicals:
- First choice: Biologic therapy (IL-17 or IL-23 inhibitors preferred)
- Alternative options: Phototherapy, systemic oral agents
- For psoriatic arthritis: Add TNF inhibitor or other appropriate agent
- Monitor response and adjust therapy as needed