[How to manage giant cell arteritis]

Danièle Allali1, Marc Blondon1, Pascale Roux-Lombard1

  • 1Service d'immunologie et d'allergologie, HUG, 1211 Genève 14.

Revue Medicale Suisse
|January 22, 2020
PubMed

Insights

Giant cell arteritis (GCA) diagnosis is crucial for timely corticosteroid treatment. Newer therapies like tocilizumab and methotrexate offer alternatives, reducing steroid dependence and relapses in GCA patients.

Area of Science:

  • Rheumatology
  • Internal Medicine
  • Vasculitis Research

Background:

  • Giant cell arteritis (GCA) is the most prevalent vasculitis affecting individuals over 50.
  • Prompt corticosteroid treatment is essential to prevent ischemic complications associated with GCA.
  • The need for accurate diagnosis is heightened due to the significant side effects of long-term corticosteroid therapy.

Purpose of the Study:

  • To review current diagnostic standards for GCA, including imaging and clinical criteria.
  • To explore established and emerging therapeutic strategies for managing GCA.
  • To discuss the role of tocilizumab, methotrexate, abatacept, and ustekinumab in GCA treatment.

Main Methods:

  • Review of histological confirmation as the gold standard for GCA diagnosis.
  • Evaluation of non-invasive imaging techniques, particularly temporal artery ultrasound.
  • Analysis of clinical studies and regulatory approvals for GCA therapies.

Main Results:

  • Temporal artery ultrasound and specific clinical criteria provide reliable non-invasive GCA diagnosis.
  • Tocilizumab, in combination with corticosteroids, is approved for GCA treatment.
  • Methotrexate has demonstrated efficacy in reducing corticosteroid dosage and relapse rates.

Conclusions:

  • Accurate diagnosis of GCA is paramount to guide appropriate and timely treatment.
  • Tocilizumab and methotrexate represent significant advancements in GCA management, offering steroid-sparing options.
  • Emerging therapies like abatacept and ustekinumab hold promise for future GCA treatment protocols.

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