
PsA Treatment Guidelines Lead with Treat-to-Target
The January issue of Arthritis and Rheumatology includes updated treatment guidelines for adults with active psoriatic arthritis. In this article, we take a comprehensive look at the guidelines.
The January issue of
Most of the recommendations were conditional in that the decision to pursue a treatment strategy should be made as a result of a discussion between physician and patient that covers pre-existing conditions, adverse events, the cost of therapy and other key factors, such as the quality of clinical evidence for the recommendation. Unless described as a “strong” recommendation, the recommendations listed here fall under “conditional.”
In adult patients with active PsA despite treatment with an oral small molecule:
• Switch to a TNF biologic over: a different oral small molecule, IL-17, IL-12/23, abatacept, tofacitinib.
• IL-17 is preferred over a different oral small molecule, IL-12/23, abatacept, tofacitinib.
• IL-12/23 is preferred over a different oral small molecule, IL-12/23, abatacept, tofacitinib
• Add apremilast to current oral small molecule therapy over switching to apremilast.
• Switch to another oral small molecule (except apremilast) over adding another oral small molecule (except apremilast) to current treatment.
• Switch to a TNF biologic monotherapy over methotrexate and a TNF biologic combination therapy.
• Switch to an IL-17 biologic monotherapy over methotrexate and an IL-17 biologic combination therapy.
• Switch to an IL-12/2 biologic monotherapy over MTX and an IL-12/23 biologic combination therapy.
For patients with active PsA who have never before been treated for the condition:
• Treat with a TNF biologic or an oral small molecule over IL-17 and IL-12/23 inhibitors.
• Methotrexate is preferred over NSAIDs.
• IL-17 inhibitors, if needed, are preferred ovver IL-12/23 biologics.
In adult patients with active PsA despite treatment with a TNF biologic monotherapy:
• Switch to a different TNF biologic over switching to an IL-17i biologic, an IL-12/23i biologic, switching to abatacept or tofacitinib or over adding methotrexate.
• Switch to an IL-17 biologic over switching to an IL-12/23i biologic, abatacept or tofacitinib.
• Switch to an IL-12/23 biologic over abatacept or tofacitinib.
• Switch to a different TNF biologic monotherapy over switching to a different TNF biologic and methotrexate combination therapy.
• Switch to an IL-17 biologic monotherapy over switching to an IL-17i biologic and methotrexate combination therapy.
• Switch to an IL-12/23 biologic monotherapy over switching to an IL-12/23 biologic and methotrexate combination therapy.
For patients on combo therapy with a TNF biologic and methotrexate:
• Switch to a different TNF biologic with methotrexate over switching to a different TNF biologic monotherapy.
• Switch to an IL-17 biologic monotherapy over an IL-17 biologic and methotrexate combination therapy.
• Switch to IL-12/23 biologic monotherapy over IL-12/23 biologic and methotrexate combination therapy.
Recommendations for patients who have been treated with IL-17 biologic monotherapy:
• Switch to a TNF biologic over switching to an IL-12/23 biologic, over a TNFi biologic over a different IL-17, over adding methotrexate to an IL-17 biologic.
• Switch to an IL-12/23 biologic over a different IL-17 biologic or over methotrexate to an IL-17 biologic.
In adult patients with active PsA who were treated with IL-12/23i biologic monotherapy:
• Switch to a TNF biologic over an IL-17 or over adding methotrexate to an IL-12/23.
• Switch to an IL-17 biologic over adding methotrexate over an IL-12/23i biologic.
Recommendations for PsA patients with axial disease or enthesitis:
• Adopt a treat-to-target strategy.
• For patients with psoriatic spondylitis/axial disease despite having been treated with NSAIDs, switch to a TNF biologic instead of an IL-17 biologic; switch to a TNF biologic over an IL-12/23 inhibitor; switch to an IL-17 biologic over an IL-12/23 inhibitor.
• For patients with predominant enthesitis who have never before taken oral small molecules or biologics, oral NSAIDs, TNFi biologics and tofacitinib are preferred over apremilast.
• Patients with predominant enthesitis despite having had treatment with oral small molecules (OSM), switch to a TNF biologic over an IL-17, IL-12/23 or another oral small molecule. IL-17 biologics are preferred over IL-12/23 or another OSM and IL-12/23 is preferred over another oral small molecule.
Recommendations for PsA patients with inflammatory bowel disease:
• Treatment naïve patients should be started on a monoclonal antibody TNF biologic over an oral small molecule.
• For PsA patients with IBD who have tried oral small molecules, it is strongly recommended that patients be switched to a monoclonal antibody TNF over a TNF biologic soluble receptor biologic, such as etanercept, or over an IL-17.
• There was a conditional recommendation to prefer a TNF over an IL-12/23 inhibitor, but then a strong recommendation to switch to an IL-12/23 biologic over an IL-17 inhibitor.
Recommendations for patients with diabetes and recurrent serious infections:
• For treatment naïve patients, first start with an oral small molecule instead of methotrexate or a TNF biologic.
• For treatment naïve patients with frequent serious infections it is strongly recommended that patients start on an oral small molecule over a TNF biologic; or, start on an IL-12/23 biologic over a TNF biologic; or, an IL-17 biologic over a TNFi biologic.
Recommendations for vaccination:
• Administering vaccines with biologics largely depends on the patient’s specific case. In most cases, biologics and vaccines can be administered together.
Recommendations for nonpharmacologic interventions:
• Pursue low-impact exercise, physical therapy, occupational therapy, weight loss for overweight patients, massage therapy, acupuncture, smoking cessation (strong recommendation).
References:
Singh JA, Guyatt G, Ogdie A, et al.




