- Design
- Prospective national register cohort
- Population
- 815 people with psoriatic arthritis starting b/tsDMARD therapy, UK
- Primary outcome
- Drug discontinuation and 12-month response
- Effect
- MDA 24%, ACR50 24% at 12 months; PDE4i vs TNFi discontinuation HR 2.25 (1.45–3.50)
The British Society for Rheumatology Psoriatic Arthritis Register followed 815 people starting a biologic or targeted synthetic DMARD, with median disease activity high at baseline.
At a median of 31 months, 65% remained on their first therapy; stopping was mostly for inefficacy (55%) or intolerance (26%). Those starting a PDE4 inhibitor were more than twice as likely to discontinue as those starting a TNF inhibitor (HR 2.25, 95% CI 1.45–3.50); other mechanisms did not differ markedly. At 12 months, 24% had reached minimal disease activity, 24% an ACR50 and 49% a PsARC response. Men, younger patients and those in work were more likely to respond; worse baseline clinical and patient-reported measures predicted non-response.
These real-world response rates are lower than in trials and underline how hard PsA remains to control. The finding on PDE4 inhibition fits its generally more modest effect.
- Set realistic expectations: about one in four reached minimal disease activity at 12 months.
- Consider a TNF inhibitor or another biologic over a PDE4 inhibitor when persistence matters.
- Assess and address high baseline pain, fatigue and function scores, which predicted non-response.
- Review at 3–6 months and switch promptly if targets are not being met.
Why it matters
Trial response rates often set patient expectations that real-world practice does not meet.
Don't overread it
Registry data — demographic predictors are associations and should not guide who is treated.
The statistics, in plain English
A hazard ratio of 2.25 means people on a PDE4 inhibitor stopped at more than twice the rate. Predictors such as sex and employment come from imputed outcomes and are associations, not reasons to withhold treatment.
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