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Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis

OBJECTIVES: To characterize the effect of ultra-short glucocorticoids followed by Tocilizumab monotherapy on the intima-media thickness (IMT) in GCA. METHODS: Eighteen GCA patients received 500 mg for 3 consecutive days (total of 1500mg) i.v. methylprednisolone on days 0–2, followed by i.v. Tocilizu...

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Autores principales: Seitz, Luca, Christ, Lisa, Lötscher, Fabian, Scholz, Godehard, Sarbu, Adela-Cristina, Bütikofer, Lukas, Kollert, Florian, Schmidt, Wolfgang A, Reichenbach, Stephan, Villiger, Peter M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566271/
https://www.ncbi.nlm.nih.gov/pubmed/34117737
http://dx.doi.org/10.1093/rheumatology/keab484
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author Seitz, Luca
Christ, Lisa
Lötscher, Fabian
Scholz, Godehard
Sarbu, Adela-Cristina
Bütikofer, Lukas
Kollert, Florian
Schmidt, Wolfgang A
Reichenbach, Stephan
Villiger, Peter M
author_facet Seitz, Luca
Christ, Lisa
Lötscher, Fabian
Scholz, Godehard
Sarbu, Adela-Cristina
Bütikofer, Lukas
Kollert, Florian
Schmidt, Wolfgang A
Reichenbach, Stephan
Villiger, Peter M
author_sort Seitz, Luca
collection PubMed
description OBJECTIVES: To characterize the effect of ultra-short glucocorticoids followed by Tocilizumab monotherapy on the intima-media thickness (IMT) in GCA. METHODS: Eighteen GCA patients received 500 mg for 3 consecutive days (total of 1500mg) i.v. methylprednisolone on days 0–2, followed by i.v. Tocilizumab (8 mg/kg) on day 3 and thereafter weekly s.c. Tocilizumab injections (162 mg) over 52 weeks. US of temporal (TAs), axillary (AAs) and subclavian (SAs) arteries was performed at baseline, on days 2–3, and at weeks 4, 8, 12, 24 and 52. The largest IMT of all segments and IMT at landmarks of AA/SA were recorded. IMT was scaled by mean normal values and averaged. Each segment was classified according to diagnostic cut-offs. RESULTS: Of the 18 GCA patients, 16 patients had TA and 6 had extracranial large artery involvement. The IMT showed a sharp decline on day 2/3 in the TAs and AAs/SAs. In TAs, this was followed by an increase to baseline levels at week 4 and a subsequent slow decrease, which was paralleled by decreasing symptoms and achievement of clinical remission. The AAs/SAs showed a new signal of vasculitis at week 4 in three patients, with an IMT increase up to week 8. CONCLUSION: Glucocorticoid pulse therapy induced a transient decrease of the IMT in TAs and AAs/SAs. Tocilizumab monotherapy resulted in a slow and steady decrease in IMT of the TAs and a smaller and delayed effect on the AAs/SAs. The data strongly support a remission-inducing effect of Tocilizumab and argue the case for US having an important role in monitoring disease activity in GCA. TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT03745586.
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spelling pubmed-85662712021-11-04 Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis Seitz, Luca Christ, Lisa Lötscher, Fabian Scholz, Godehard Sarbu, Adela-Cristina Bütikofer, Lukas Kollert, Florian Schmidt, Wolfgang A Reichenbach, Stephan Villiger, Peter M Rheumatology (Oxford) Clinical Science OBJECTIVES: To characterize the effect of ultra-short glucocorticoids followed by Tocilizumab monotherapy on the intima-media thickness (IMT) in GCA. METHODS: Eighteen GCA patients received 500 mg for 3 consecutive days (total of 1500mg) i.v. methylprednisolone on days 0–2, followed by i.v. Tocilizumab (8 mg/kg) on day 3 and thereafter weekly s.c. Tocilizumab injections (162 mg) over 52 weeks. US of temporal (TAs), axillary (AAs) and subclavian (SAs) arteries was performed at baseline, on days 2–3, and at weeks 4, 8, 12, 24 and 52. The largest IMT of all segments and IMT at landmarks of AA/SA were recorded. IMT was scaled by mean normal values and averaged. Each segment was classified according to diagnostic cut-offs. RESULTS: Of the 18 GCA patients, 16 patients had TA and 6 had extracranial large artery involvement. The IMT showed a sharp decline on day 2/3 in the TAs and AAs/SAs. In TAs, this was followed by an increase to baseline levels at week 4 and a subsequent slow decrease, which was paralleled by decreasing symptoms and achievement of clinical remission. The AAs/SAs showed a new signal of vasculitis at week 4 in three patients, with an IMT increase up to week 8. CONCLUSION: Glucocorticoid pulse therapy induced a transient decrease of the IMT in TAs and AAs/SAs. Tocilizumab monotherapy resulted in a slow and steady decrease in IMT of the TAs and a smaller and delayed effect on the AAs/SAs. The data strongly support a remission-inducing effect of Tocilizumab and argue the case for US having an important role in monitoring disease activity in GCA. TRIAL REGISTRATION: ClinicalTrials.gov, www.clinicaltrials.gov, NCT03745586. Oxford University Press 2021-10-02 /pmc/articles/PMC8566271/ /pubmed/34117737 http://dx.doi.org/10.1093/rheumatology/keab484 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Science
Seitz, Luca
Christ, Lisa
Lötscher, Fabian
Scholz, Godehard
Sarbu, Adela-Cristina
Bütikofer, Lukas
Kollert, Florian
Schmidt, Wolfgang A
Reichenbach, Stephan
Villiger, Peter M
Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
title Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
title_full Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
title_fullStr Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
title_full_unstemmed Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
title_short Quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
title_sort quantitative ultrasound to monitor the vascular response to tocilizumab in giant cell arteritis
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566271/
https://www.ncbi.nlm.nih.gov/pubmed/34117737
http://dx.doi.org/10.1093/rheumatology/keab484
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