Treatment of Psoriatic Arthritis
For treatment-naïve patients with active psoriatic arthritis, initiate a TNF inhibitor (adalimumab, etanercept, or infliximab) as first-line therapy unless severe psoriasis, contraindications to TNF inhibitors, or patient preference for oral therapy exists. 1
Initial Treatment Selection Algorithm
For Patients WITHOUT Severe Psoriasis (PASI <12 or BSA <10)
First-line: TNF Inhibitor
- Adalimumab 40 mg subcutaneously every other week 2
- Etanercept 50 mg subcutaneously weekly 3
- Infliximab (dosing per protocol) 1
- TNF inhibitors reduce signs and symptoms, inhibit radiographic progression, and improve physical function 4
- Can be used as monotherapy or combined with methotrexate at reduced doses (10-15 mg weekly) 5
Alternative first-line if contraindications to TNF inhibitors exist:
- Oral small molecule DMARDs, with methotrexate 15-25 mg weekly with folic acid supplementation preferred when clinically relevant skin involvement is present 5, 1
- Sulfasalazine or leflunomide have Level A evidence for peripheral arthritis 4, 5
For Patients WITH Severe Psoriasis (PASI ≥12 and BSA ≥10)
First-line: IL-17 or IL-12/23 Inhibitors
- These agents are preferred over TNF inhibitors when severe psoriasis coexists 1
- IL-12/23 inhibitors offer less frequent administration and are particularly preferred if concomitant inflammatory bowel disease exists 1
Special Population Considerations
Patients with concomitant diabetes:
- Use sulfasalazine or leflunomide instead of methotrexate due to higher risk of fatty liver disease and hepatotoxicity 5
Patients preferring oral therapy:
- Oral small molecules are appropriate when disease is not severe 5
- Methotrexate remains the preferred conventional DMARD 1
Patients with frequent serious infections or contraindications to biologics:
- Oral small molecules are strongly recommended over biologics 5
- Contraindications include congestive heart failure, demyelinating disease, or recurrent infections 5
Treatment Escalation for Inadequate Response
After Oral Small Molecule Failure
Switch to TNF inhibitor over another oral small molecule, IL-17 inhibitor, or IL-12/23 inhibitor if active PsA persists despite adequate trial (>3 months, with >2 months at standard target dose) 4, 1
Exception: Consider IL-17 or IL-12/23 inhibitors instead if severe psoriasis is present 1
After TNF Inhibitor Failure
- Consider switching to IL-17 inhibitor or IL-12/23 inhibitor 1
- If concomitant active IBD exists, prefer IL-12/23 inhibitor 1
Disease-Specific Treatment Approaches
Peripheral Arthritis
- Mild disease: NSAIDs for symptomatic relief, though they do not prevent structural joint damage 4, 5
- Intra-articular glucocorticoid injections for persistently inflamed joints, avoiding injection through psoriatic plaques 5
- Moderate to severe disease: Initiate DMARDs rapidly, progressing to TNF inhibitors if inadequate response 5
Axial Disease
- First-line: NSAIDs and physiotherapy 4, 6
- Traditional oral DMARDs (methotrexate, leflunomide, sulfasalazine) are NOT effective for axial manifestations and should not be used 4, 6
- Second-line: TNF inhibitors for moderate to severe spinal disease with insufficient response to NSAIDs 6
- Consider IL-17 inhibitor if relevant skin involvement coexists with axial disease 6
- Monitor using BASDAI score; active disease defined as BASDAI >4, treatment response as BASDAI <3 or reduction by 2 points after 6 weeks 4, 6
Enthesitis and Dactylitis
- First-line: NSAIDs and local measures 5
- Resistant cases: Progress to DMARDs 5
- Severe or refractory cases: Consider TNF inhibitors 5
Critical Safety Considerations
Before Initiating TNF Inhibitors
Mandatory screening:
- Test for latent tuberculosis before and during therapy; initiate treatment for latent TB prior to TNF inhibitor use 2, 3
- Consider empiric anti-fungal therapy in patients at risk for invasive fungal infections who develop severe systemic illness 2, 3
- Complete age-appropriate vaccinations prior to initiating treatment 3
Medications to AVOID
- Systemic corticosteroids are NOT typically recommended due to potential for post-steroid psoriasis flare 4
- Gold salts, chloroquine, and hydroxychloroquine are NOT recommended for PsA 4
High-Risk Scenarios
- Lymphoma and other malignancies, some fatal, have been reported in children and adolescents treated with TNF blockers 2, 3
- Hepatosplenic T-cell lymphoma risk is particularly elevated in adolescent and young adult males with IBD receiving TNF blockers plus azathioprine or 6-mercaptopurine 2
Treatment Goals and Monitoring
Primary goal: Achieve remission or minimal/low disease activity through regular monitoring and appropriate treatment adjustment 1
Assessment tools:
- DAS28, EULAR response criteria, or ACR20/50/70 for peripheral arthritis 4
- BASDAI for axial disease 4, 6
- Radiographic assessment for joint damage progression 4
Poor prognostic factors requiring aggressive treatment:
- Polyarticular disease 4, 5
- Elevated inflammatory markers (ESR) 4, 5
- Previous treatment failures 5
- Existing joint damage 4, 5
- Diminished quality of life 4, 5
Adjunctive Non-Pharmacologic Interventions
- Smoking cessation strongly recommended for all patients 5
- Low-impact exercise (tai chi, yoga, swimming) preferred over high-impact exercise 5
- Weight loss in overweight or obese patients may potentially increase pharmacologic response 5
- Physical therapy as first-line intervention for axial disease to improve function and reduce pain 6
Comorbidity Management
Account for comorbidities when selecting treatment: