Table 4

Research agenda indicating priorities for future research in PsA

ThemeQuestion
Responsibility
  • Role of the rheumatologist vs other specialists in the management of PsA.

Pathogenesis
  • Pathogenesis of different tissue involvements in PsA.

  • Pathogenesis of axial disease.

  • Microbiome relationship to disease onset and progression.

  • Prediction markers of response on synovial histopathology.

  • Identification of new therapeutic targets.

  • Understanding the biopathology of treatment-refractory PsA.

  • Genetics of PsA.

Very early PsA
  • Biomarkers for pre-PsA.

  • Defining screening strategies for PsA among patients with psoriasis: is screening needed, and if so in which populations, how and when?

  • Criteria for early diagnosis of PsA and role of imaging.

  • Prevention of progression from psoriasis to PsA: pre-PsA therapy/interception (efficacy of DMARDs in preventing progression from Pso to PsA).

  • Window of opportunity studies.

Drug ordering/response prediction and biomarkers
  • Research on the effect of sex on treatment choices, treatment efficacy and treatment maintenance.

  • Incorporating ultrasonography in decision-making.

  • Biomarkers for prediction of disease and response.

  • Prediction of response with genetics and polygenetics.

Prognosis
  • Prognostic factors of progressive disease, structural damage and unfavourable functional outcomes.

  • Predicting response to treatment (predicting response to NSAIDs, to csDMARDs, to the different bDMARDs, to tsDMARDs).

  • Prognosis of early-onset (juvenile) PsA.

First DMARD choices
  • Biosimilars vs methotrexate as first choice—strategy trials.

  • Comparing direct and indirect costs, efficacy, side effects in employed, early, severe, bio-naïve PsA patient groups treated with methotrexate or biosimilars. Is there any advantage of using methotrexate over biosimilars in this group?

Outcomes in PsA
  • Development/validation of composite scores of disease activity in PsA.

  • Consensus on core outcomes in PsA trials.

  • Coprimary outcomes for skin and joints.

  • Efficacy of apremilast on structural changes.

  • Drug-free remission as an outcome in PsA.

Treatments
  • Efficacy of csDMARDs for dactylitis.

  • Assessing combinations of csDMARDs with biologics compared with biologics monotherapy.

  • Associations of bDMARDs.

Contextual factors in PsA
  • Sex and gender.

  • Age.

Safety
  • Differential JAKi safety in PsA and across drugs.

  • Tyrosine-kinase inhibition safety in PsA.

  • Long-term safety trials in PsA.

Axial PsA
  • Pathogenesis of axial PsA vs axSpA.

  • Criteria for differentiation and overlap between axSpA and PsA.

  • JAKis in axial PsA.

  • Assessment of spinal disease: defining the similarities and differences with axSpA.

Comorbidities
  • Impact of comorbidities on drug choice.

  • Effect of metabolic intervention on disease activity.

  • Effect of different DMARDs on cardiovascular risk.

  • Influence of non-pharmacological interventions on multimorbidity.

  • Entheseal PsA: overlap with widespread pain syndrome and role of imaging in the diagnosis.

  • Treatment of pain which does not respond to usual therapies.

  • Fatigue in PsA.

  • Unravelling complexities of difficult-to-manage PsA.

Switches
  • Repeat switching within a DMARD class.

  • Switching and cycling between drugs.

  • axSpA, axial spondyloarthritis; bDMARDs, biological disease-modifying antirheumatic drugs; csDMARDs, conventional synthetic disease-modifying antirheumatic drugs; DMARDs, disease-modifying antirheumatic drugs; JAKi, Janus kinase inhibitor; NSAIDs, non-steroidal anti-inflammatory drugs; PsA, psoriatic arthritis; tsDMARDs, targeted synthetic disease-modifying antirheumatic drugs.