Psoriasis Treatment
For mild psoriasis (<5% body surface area), start with combination topical therapy using calcipotriene/betamethasone dipropionate once daily for 4-8 weeks, which achieves clear or almost clear skin in 48-74% of patients. 1
Disease Severity Classification
- Mild psoriasis is defined as <5% body surface area (BSA) involvement in asymptomatic patients who are candidates for topical therapy alone 1, 2
- Moderate-to-severe psoriasis is defined as ≥5% BSA or involvement of vulnerable areas (face, genitals, hands, feet) 1, 3
- Symptomatic psoriasis (pain, bleeding, itching) warrants systemic or phototherapy consideration even with limited BSA involvement 1, 3, 2
- Quality of life impact should drive treatment intensity regardless of physical extent 1, 3
Treatment Algorithm by Severity
Mild Psoriasis (<5% BSA)
First-Line Topical Therapy:
- Calcipotriene/betamethasone dipropionate combination product once daily for 4-8 weeks is the optimal first-line choice 1, 2
- This combination enhances efficacy and reduces irritation compared to monotherapy 1
- After achieving initial control, transition to weekend-only high-potency corticosteroid (twice daily on weekends) with weekday vitamin D analogue therapy (twice daily on weekdays) to minimize corticosteroid exposure while maintaining efficacy 2
Site-Specific Modifications:
- Scalp psoriasis: Calcipotriene foam or calcipotriene plus betamethasone dipropionate gel for 4-12 weeks 1, 2
- Facial/intertriginous psoriasis: Low-potency corticosteroids or tacrolimus to avoid skin atrophy 1, 3, 2
- Nail psoriasis: Calcipotriene combined with betamethasone dipropionate, though efficacy is limited due to poor nail matrix penetration 2
- Body/extremities: Class 2-5 (moderate to high potency) corticosteroids initially; for thick chronic plaques, use class 1 ultrahigh-potency agents like clobetasol propionate 0.05% or halobetasol propionate 0.05% 2
Moderate-to-Severe Psoriasis (≥5% BSA)
First-Line: Phototherapy
- Narrowband UVB or PUVA phototherapy 1, 3
- The 308-nm excimer laser allows selective targeting of localized resistant areas such as scalp and skin folds 2
Second-Line: Traditional Systemic Agents
- Methotrexate (FDA-approved since 1972, competitive inhibitor of dihydrofolate reductase) requires regular monitoring of complete blood count, liver function tests, and serum creatinine 1, 2
- Cyclosporine 3-5 mg/kg/day for rapid onset, particularly effective for erythrodermic psoriasis; use in short 3-4 month "interventional" courses; requires monitoring of blood pressure, renal function, and lipid profile 1, 2
- Acitretin decreases keratinocyte hyperproliferation but is absolutely contraindicated in women of childbearing potential due to teratogenicity 1, 2
Third-Line: Biologic Agents
- IL-17 inhibitors, IL-23 inhibitors, IL-12/23 inhibitors, and TNF inhibitors 1, 3
- Adalimumab (HUMIRA): 80 mg initial dose, followed by 40 mg every other week starting one week after initial dose for plaque psoriasis 4
- For psoriatic arthritis, adalimumab is effective for both skin and joint symptoms 3, 4
Combination Therapy Strategies for Moderate-to-Severe Disease
Adding topical therapy to biologics significantly accelerates clearance:
- Adding ultrahigh-potency (class 1) topical corticosteroid to standard dose etanercept for 12 weeks (Level I evidence) 1, 2
- Adding calcipotriene/betamethasone to standard dose adalimumab for 16 weeks accelerates plaque clearance 1, 2
- Adding topical calcipotriene to standard dose methotrexate therapy (Level I evidence) 1, 2
- All topical corticosteroids can be used in combination with any biologics 1, 2
Psoriatic Arthritis Treatment
- Mild joint symptoms: NSAIDs 1, 3
- Moderate-to-severe joint involvement: DMARDs (methotrexate, sulfasalazine, leflunomide) 1, 3
- Inadequate response to at least one DMARD: TNF inhibitors 1, 3
- Severe enthesitis failing other therapies: Consider TNF inhibitor 1
Critical Pitfalls to Avoid
- Never use systemic corticosteroids in psoriasis—they cause disease flare during taper 1, 3
- Never combine salicylic acid with calcipotriene simultaneously—the acidic pH inactivates calcipotriene and eliminates its effectiveness 2
- Limit continuous high-potency corticosteroid use to maximum 4 weeks to prevent skin atrophy, striae, telangiectasia, and HPA axis suppression 1, 2
- Do not use high-potency corticosteroids on face or flexures—use low-potency agents or tacrolimus instead 2
- Apply vitamin D analogues after phototherapy, not before, to avoid inactivation 3, 2
- Maximum vitamin D analogue use: 100g per week to avoid hypercalcemia 2
- All commonly used systemic agents are absolutely contraindicated in pregnancy 1
- Long-term use of high-potency corticosteroids beyond 12 weeks requires careful physician supervision 2