Spondyloarthritis & psoriatic arthritis

The use of ASDAS to evaluate disease activity and response to treatment in patients with axial spondyloarthritis starting the first biological drug: Are ASAS recommendations being followed?

Semin Arthritis RheumPublished Registry-based cohort study

Authors' conclusion

ASDAS is widely assessed in axSpA patients starting bDMARDs by Portuguese rheumatologists. Most patients respond within 3 months but waiting until 6 months to determine treatment continuation is reasonable.

Study context

Population
Patients with axial spondyloarthritis (axSpA) from the Reuma.pt registry who initiated their first bDMARD and attended baseline, 3-month and 6-month visits
Participants
666 patients
Outcome
Proportion with ASDAS calculated at baseline and at least once within two follow-up visits after starting first bDMARD
Methodological detailsReuma.pt registry
  • Reuma.pt registry

Main finding

As reported in the abstract

ASDAS availability

ASDAS at baseline

N = 540; 81 %

ASDAS at baseline and at 3 M and/or 6 M

493

74 %

Observational data: associations, not effects.

Further findings

Alternative outcome measures when ASDAS absent

No alternative outcome measure was predominantly used

Meeting ASAS continuation criteria (∆ASDAS ≥1.1), among 336 with complete ASDAS evaluation · 3 M and 6 M

%

Met criteria at 3 M
58
Met criteria at 6 M
60
Response maintenance between 3 M and 6 M
86
Non-responders at 3 M (n=147) responding at 6 M
25

Characteristics of responders at both timepoints vs others

Male
65 % vs 45 %
Mean age
35 vs 38 years

Original publication

The use of ASDAS to evaluate disease activity and response to treatment in patients with axial spondyloarthritis starting the first biological drug: Are ASAS recommendations being followed? Semin Arthritis Rheum. Published 18 July 2025. doi:10.1016/j.semarthrit.2025.152781

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