Vasculitis & polymyalgia rheumatica

Comparison of methotrexate and azathioprine as the first-line steroid-sparing immunosuppressive agents in patients with Takayasu's arteritis

Semin Arthritis RheumPublished Retrospective cohort study

Authors' conclusion

Remission, relapse, radiographic progression and drug survival rates of AZA and MTX were similar for patients with TAK receiving an IS agent as the first-line f therapy. The rate of vascular surgery was higher and the rate of GC dose reduction was lower with AZA compared to MTX at the end of the follow-up.

Study context

Population
TAK patients receiving an immunosuppressive (IS) agent plus glucocorticoids (GCs) as initial therapy, 10 tertiary centresF/M: 260/41
Participants
301 patients
Exposure
Methotrexate (MTX) vs AZA as first-line IS agent with GCs
  • MTXn = 204
  • AZAn = 77reference
Methodological detailsmulticentre, matched analysis (age, gender, diffuse aortic involvement)
  • Multicentre
  • Matched analysis (age, gender, diffuse aortic involvement)

Main finding

As reported in the abstract

  • Remission, relapse, radiographic progression and adverse effect rates similar between MTX and AZA

Observational data: associations, not effects.

Further findings

Vascular surgery

P = 0.001

GCs ≤5 mg/day at end of follow-up

P = 0.034

Drug survival · median 48 months

P = 0.34

Events

OutcomeMTXAZA
IS discontinued due to remission126
IS discontinued due to remission — Total discontinued
18
IS discontinued due to remission — Still in remission at end of mean 69.4 (±50.9) months follow-up
16

Vascular surgery

Vascular surgery rate also higher with AZA in matched analysis

IS discontinued due to remission

Relapse after discontinuation (at 2 and 6 months)

Safety

Adverse effect rates similar between MTX and AZA

Original publication

Comparison of methotrexate and azathioprine as the first-line steroid-sparing immunosuppressive agents in patients with Takayasu's arteritis. Semin Arthritis Rheum. Published 8 April 2024. doi:10.1016/j.semarthrit.2024.152446

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.