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Abstract Number: 2633

Comparative 3-year Safety Outcomes in Patients with Ankylosing Spondylitis Initiating JAK Inhibitor or TNF Inhibitor Therapy

Hsin-Hua Chen, Taichung Veterans General Hospital, Taichung, Taiwan (Republic of China)

Meeting: ACR Convergence 2025

Keywords: Ankylosing spondylitis (AS), Anti-TNF Drugs, Epidemiology, Outcome measures, risk assessment

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Session Information

Date: Tuesday, October 28, 2025

Title: Abstracts: Spondyloarthritis Including Psoriatic Arthritis – Diagnosis, Manifestations, & Outcomes II: Advances in Axial Spondyloarthritis (2633–2638)

Session Type: Abstract Session

Session Time: 3:00PM-3:15PM

Background/Purpose: To compare safety outcomes in patients with ankylosing spondylitis (AS) initiating Janus kinase inhibitors (JAKi) versus tumor necrosis factor inhibitors (TNFi).

Methods: This retrospective cohort study utilized data from the TriNetX Global Collaborative Network, comparing patients initiating JAKi (n=299) versus TNFi (n=299) after propensity score matching for age, sex, race, diabetes mellitus, hypertension, psoriasis, inflammatory bowel disease, uveitis, and hyperlipidemia, . Patients were followed for up to three years. Outcomes included mortality, major adverse cardiovascular events (MACE), venous thromboembolism (VTE), malignancy, gastrointestinal bleeding, hepatitis (non-infectious), serious infections (sepsis, pneumonia, herpes zoster), dermatologic events, and neuropsychiatric disorders. Kaplan–Meier analysis provided hazard ratios (HRs) with 95% confidence intervals (CIs).

Results: JAKi initiation was associated with significantly increased all-cause mortality (4.3% vs. 3.3%; HR 4.94, 95% CI 1.59–15.37) and gastrointestinal bleeding (3.4% vs. 0%; p=0.002). Conversely, malignancy occurred exclusively among TNFi initiators (3.4% vs. 0%; p=0.001). Herpes zoster infection showed a non-significant trend toward higher incidence in JAKi users (6.0% vs. 5.0%; HR 1.90, 95% CI 0.95–3.83). No significant differences emerged in MACE, VTE, serious bacterial infections (including pneumonia and sepsis), dermatologic events, or hepatitis. Anxiety/insomnia diagnoses were numerically lower with JAKi (14.3% vs. 24.1%), but without statistical significance.

Conclusion: Compared with TNFi, JAKi therapy in AS was associated with increased mortality and gastrointestinal bleeding, but lower short-term malignancy incidence. Infection-related outcomes were similar, aside from a potential herpes zoster risk. These findings highlight distinct safety trade-offs, underscoring the need for individualized treatment choices in AS.

Supporting image 1Table 1: Baseline Characteristics Before and After PSM (JAKi vs TNFi).

Supporting image 2Table 2. Three-year safety outcomes in patients with ankylosing spondylitis initiating JAK inhibitors or TNF inhibitors after propensity score matching shown as hazard ratios with 95% confidence intervals (JAKi vs. TNFi)


Disclosures: H. Chen: None.

To cite this abstract in AMA style:

Chen H. Comparative 3-year Safety Outcomes in Patients with Ankylosing Spondylitis Initiating JAK Inhibitor or TNF Inhibitor Therapy [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/comparative-3-year-safety-outcomes-in-patients-with-ankylosing-spondylitis-initiating-jak-inhibitor-or-tnf-inhibitor-therapy/. Accessed .
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