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NCT Number: NCT07459335

TArget Trial Emulation Comparing Effectiveness of Tocilizumab vs Methotrexate In Corticosteroid-Treated GCA Patients

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).

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Key information

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥50 years Incident hospitalization for giant cell arteritis Initiation of tocilizumab or methotrexate within 6 months Received systemic corticosteroids ≥20 mg/day within 30 days following hospital discharge

Exclusion criteria

  • Prior use of tocilizumab or methotrexate Age >90 years Length of stay >30 days Not discharged home Prior aortic disease or vascular imaging within 2 years Initiation of both treatments during grace period

Treatment and study plan

Primary outcomes

  1. Major Adverse Cardiovascular Events (MACE)

    Time frame: 2 years

    Major Adverse Cardiovascular Events (MACE) Composite of myocardial infarction, ischemic stroke, or all-cause death

Secondary outcomes

  1. Coronary events

    Time frame: 2 years

    Coronary events (myocardial infarction or unstable angina)

  2. Ischemic stroke

    Time frame: 2 years

    Ischemic stroke assessed at 2 years

  3. All-cause mortality

    Time frame: 2 years

    All-cause mortality assessed at 2 years

  4. Aortic events

    Time frame: 2 years

    Aortic events (aneurysm or dissection)

  5. Major vascular relapse

    Time frame: 2 years

    Major vascular relapse assessed at 2 years

  6. Lower limb revascularization

    Time frame: 2 years

    • Lower limb revascularization assessed at 2 years
  7. Anterior ischemic optic neuropathy (AION)

    Time frame: 2 years

    Anterior ischemic optic neuropathy (AION) assessed at 2 years

  8. Peripheral artery disease events

    Time frame: 2 years

    Peripheral artery disease events assessed at 2 years

  9. Cancer incidence

    Time frame: 2 years

    Cancer incidence at 2 years

Sponsors and collaborators

Lead sponsor

Groupe français d'étude des Maladies Inflammatoires de loeil

Other

Registry information

Official study title

Comparative Effect of Tocilizumab Versus Methotrexate on Major Adverse Cardiovascular Events in Giant Cell Arteritis: A Nationwide Target Trial Emulation Using the French SNDS

Acronym: TACTIC-GCA

Important dates

Study start
2012
Primary completion
2024
Study completion
2024
First posted
Mar 9, 2026
Registry last updated
Mar 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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