This nationwide observational study emulates a target trial to compare the effect of tocilizumab versus methotrexate initiation on major adverse cardiovascular events (MACE) in patients with incident giant cell arteritis using the French National Health Data System (SNDS).
Study Design and Data Source This study is a retrospective nationwide cohort study using the SNDS database covering approximately 99% of the French population. We emulated a hypothetical randomized trial comparing two treatment strategies: initiation of tocilizumab versus methotrexate within 6 months after hospital discharge for incident giant cell arteritis. Eligible patients aged ≥50 years hospitalized for incident GCA between 2012 and 2024 were included. Statistical Analysis A clone-censor-weight approach was used to account for treatment initiation timing and avoid immortal time bias. Inverse probability of censoring weights were applied to adjust for informative censoring. Treatment effects were estimated using weighted Kaplan-Meier methods and Cox proportional hazards models. Outcomes The primary outcome was the occurrence of major adverse cardiovascular events (MACE), defined as myocardial infarction, ischemic stroke, or all-cause death. Secondary outcomes included individual cardiovascular components, aortic events, and major vascular relapse. Regulatory Compliance This study was conducted using the SNDS through the permanent access granted to Assistance Publique - Hôpitaux de Paris (AP-HP), in accordance with French Decree No. 2016-1871 and French Public Health Code (Art. R. 1461-13 and 14). The study was registered in the AP-HP internal registry of research projects before initiation. In compliance with the GDPR and French regulations, individual informed consent was not required as all data were fully anonymized
Study Type
OBSERVATIONAL
Enrollment
1,667
APHP_ Hôpital Saint-Antoine
Paris, France
APHP_ Hôpital Pitié-Salpêtrière
Paris, France
Major Adverse Cardiovascular Events (MACE)
Major Adverse Cardiovascular Events (MACE) Composite of myocardial infarction, ischemic stroke, or all-cause death
Time frame: 2 years
Coronary events
Coronary events (myocardial infarction or unstable angina)
Time frame: 2 years
Ischemic stroke
Ischemic stroke assessed at 2 years
Time frame: 2 years
All-cause mortality
All-cause mortality assessed at 2 years
Time frame: 2 years
Aortic events
Aortic events (aneurysm or dissection)
Time frame: 2 years
Major vascular relapse
Major vascular relapse assessed at 2 years
Time frame: 2 years
Lower limb revascularization
7\. Lower limb revascularization assessed at 2 years
Time frame: 2 years
Anterior ischemic optic neuropathy (AION)
Anterior ischemic optic neuropathy (AION) assessed at 2 years
Time frame: 2 years
Peripheral artery disease events
Peripheral artery disease events assessed at 2 years
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Time frame: 2 years
Cancer incidence
Cancer incidence at 2 years
Time frame: 2 years