Treatment of Rheumatoid Arthritis
The optimal treatment for rheumatoid arthritis begins with methotrexate as first-line therapy, followed by combination DMARDs or biologics for inadequate response, with the goal of achieving low disease activity or remission through a treat-to-target approach. 1, 2, 3
Initial Treatment Approach
- Start methotrexate (MTX) as first-line therapy at 15-25 mg weekly (or maximum tolerated dose), as it is the most effective conventional disease-modifying antirheumatic drug (DMARD) 1, 3
- Consider switching to subcutaneous MTX administration if oral MTX provides inadequate response, as it has better bioavailability at higher doses 1, 4
- Add folic acid supplementation to reduce MTX-related side effects 3
- Evaluate disease activity using validated measures such as the Simplified Disease Activity Index (SDAI) or Clinical Disease Activity Index (CDAI) to guide treatment decisions 1
Management of Acute Flares
- For acute flares, low-dose glucocorticoids (≤10 mg/day prednisone or equivalent) can provide rapid symptom relief 2
- Use glucocorticoids at the lowest possible dose and for the shortest duration (less than 3 months) to minimize adverse effects 2
- For isolated joint involvement, consider intra-articular glucocorticoid injections for targeted relief 1, 2
Treatment Escalation for Inadequate Response
- If MTX monotherapy provides inadequate response after 3 months, consider the following options:
Option 1: Triple DMARD Therapy
- Add sulfasalazine (SSZ) and hydroxychloroquine (HCQ) to MTX for triple therapy 1, 2, 5
- This combination has shown superior efficacy compared to MTX alone or dual therapy with SSZ and HCQ 5
Option 2: Biologic DMARDs
- For patients with moderate to high disease activity despite optimized MTX, consider adding a biologic DMARD 1, 6
- TNF inhibitors (such as adalimumab) are commonly used first-line biologics in combination with MTX 7, 8
- For patients with inadequate response to TNF inhibitors, consider switching to a different class of biologic:
Monitoring and Treatment Goals
- Monitor disease activity every 1-3 months in active disease 1, 6
- The treatment target should be low disease activity or remission 2, 3
- Adjust therapy if target is not achieved within 3 months 1, 6
- Consider cautious de-escalation of therapy for patients in sustained remission (≥1 year), but be prepared to resume previous treatment if flares occur 1
Important Considerations and Pitfalls
- Screen for latent tuberculosis, hepatitis B, and other infections before starting biologic therapy 7, 9
- When switching biologics, consider using agents with different mechanisms of action rather than switching within the same class 1
- Monitor for potential adverse effects:
- Biomarker-guided therapy: Consider that seronegative patients with inadequate response to TNF inhibitors may respond better to abatacept or tocilizumab rather than rituximab 1