Vasculitis & polymyalgia rheumatica

Janus Kinase inhibitors in refractory Takayasu arteritis: a systematic review and proportion meta-analysis of efficacy and safety

Rheumatology (Oxford)Published systematic review and meta-analysis

Authors' conclusion

JAK inhibitors demonstrate promising clinical efficacy and a potentially manageable safety profile in refractory TAK. However, the available evidence is predominantly observational and therefore subject to confounding and other sources of bias. High-quality prospective and randomized studies are needed to establish their efficacy, comparative effectiveness, and long-term safety.

Study context

Population
Adults with refractory Takayasu arteritis (TAK) treated with JAK inhibitors, in observational cohorts, non-randomized interventional studies, and case series including ≥5 patientspatients in eleven included studies
Participants
185 adults
Outcome
Clinical remission (pooled rate)
Methodological detailsproportion meta-analysis, random-effects models, Risk of bias assessed using Cochrane ROBINS-I and Joanna Briggs Institute tools, GRADE
  • Proportion meta-analysis
  • Random-effects models
  • Risk of bias assessed using Cochrane ROBINS-I and Joanna Briggs Institute tools
  • GRADE

Pooled result

As reported in the abstract

Pooled clinical remission rate

64%

95% CI 55%–72%; I²=0%

Further pooled results

Complete and partial remission (pooled rates)

Complete remission
65% (95% CI, 55%-74%)
Partial remission
8% (95% CI, 4%-17%)

No response and relapse (pooled rates)

No response
24%
Relapse
14%

Imaging improvement or stabilization

Imaging improvement or stabilization
44%

Glucocorticoid-sparing effects

Glucocorticoid-sparing effects
56%

GRADE certainty

GRADE certainty was very low for all assessed outcomes

Safety

Adverse events
10%
Discontinued treatment because of adverse events
7%

Original publication

Janus Kinase inhibitors in refractory Takayasu arteritis: a systematic review and proportion meta-analysis of efficacy and safety. Rheumatology (Oxford). Published 13 November 2026. doi:10.1093/rheumatology/keag640

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