Giant cell arteritis: Current treatment and management
Cristina Ponte, Ana Filipa Rodrigues, Lorraine O’Neill, Raashid Ahmed Luqmani
Cristina Ponte, Ana Filipa Rodrigues, Lorraine O’Neill,
Raashid Ahmed Luqmani, Nufield Department of Orthopaedics
Rheumatology and Musculoskeletal Sciences, Botnar Research
Centre, University of Oxford, Oxford OX1 2JD, United Kingdom
Cristina Ponte, Department of Rheumatology, Hospital de Santa
Maria, CHLN, Lisbon Academic Medical Centre, 1649-035
Lisbon, Portugal
Ana Filipa Rodrigues, Department of Internal Medicine,
Hospital das Caldas da Rainha, Centro Hospitalar Oeste,
2500-176 Caldas da Rainha, Portugal
Lorraine O’Neill, Department of Rheumatology, St Vincent’s
University Hospital, Dublin, Ireland
Author contributions: All authors contributed to the writing of
this review manuscript.
Conlict-of-interest: The authors have no conlicts of interest.
Open-Access: This article is an open-access article which was
selected by an in-house editor and fully peer-reviewed by external
reviewers. It is distributed in accordance with the Creative
Commons Attribution Non Commercial (CC BY-NC 4.0) license,
which permits others to distribute, remix, adapt, build upon this
work non-commercially, and license their derivative works on
different terms, provided the original work is properly cited and
the use is non-commercial. See: http://creativecommons.org/
licenses/by-nc/4.0/
Correspondence to: Cristina Ponte, MD, Nufield Department
of Orthopaedics, Rheumatology and Musculoskeletal Sciences,
Botnar Research Centre, University of Oxford, Nuffield
Orthopaedic Centre, Windmill Road, Oxford OX3 7LD,
United Kingdom. cristinadbponte@gmail.com
Telephone: +44-1865-227374
Received: January 5, 2015
Peer-review started: January 20, 2015
First decision: January 30, 2015
Revised: February 28, 2015
Accepted: March 30, 2015
Article in press: April 2, 2015
Published online: June 16, 2015
Abstract
Glucocorticoids remain the cornerstone of medical
therapy in giant cell arteritis (GCA) and should be
started immediately to prevent severe consequences of
the disease, such as blindness. However, glucocorticoid
therapy leads to signiicant toxicity in over 80% of the
patients. Various steroid-sparing agents have been
tried, but robust scientific evidence of their efficacy
and safety is still lacking. Tocilizumab, a monoclonal
IL-6 receptor blocker, has shown promising results in
a number of case series and is now being tested in a
multi-centre randomized controlled trial. Other targeted
treatments, such as the use of abatacept, are also
now under investigation in GCA. The need for surgical
treatment is rare and should ideally be performed in a
quiescent phase of the disease. Not all patients follow
the same course, but there are no valid biomarkers to
assess therapy response. Monitoring of disease progress
still relies on assessing clinical features and measuring
inflammatory markers (C-reactive protein and eryth-
rocyte sedimentation rate). Imaging techniques ( e.g. ,
ultrasound) are clearly important screening tools for
aortic aneurysms and assessing patients with large-
vessel involvement, but may also have an important
role as biomarkers of disease activity over time or in
response to therapy. Although GCA is the most common
form of primary vasculitis, the optimal strategies for
treatment and monitoring remain uncertain.
Key words: Giant cell arteritis; Therapy; Disease mana-
gement; Glucocorticoids; Immunosuppressive agents
© The Author(s) 2015. Published by Baishideng Publishing
Group Inc. All rights reserved.
Core tip: Giant cell arteritis (GCA) is the most common
form of primary systemic vasculitis. Treatment with
high doses of glucocorticoids should be initiated as
early as possible to prevent ischaemic manifestations,
such as blindness (occurring in up to 20%). However,
glucocorticoid therapy leads to signiicant toxicity in over
80% of the patients. Various steroid-sparing agents
have been tried, but robust scientiic evidence of their
eficacy and safety is still lacking. Not all patients follow
the same course, but there are no valid biomarkers
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DOI: 10.12998/wjcc.v3.i6.484
World J Clin Cases 2015 June 16; 3(6): 484-494
ISSN 2307-8960 (online)
© 2015 Baishideng Publishing Group Inc. All rights reserved.
World Journal of
Clinical Cases
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June 16, 2015|Volume 3|Issue 6| WJCC|www.wjgnet.com 484