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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.
Afiliação
  • Seitz L; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Christ L; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Lötscher F; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Scholz G; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Sarbu AC; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Bütikofer L; CTU Bern, University of Bern, Bern, Switzerland.
  • Kollert F; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Schmidt WA; Medical Centre for Rheumatology, Immanuel Krankenhaus Berlin, Berlin-Buch, Germany.
  • Reichenbach S; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
  • Villiger PM; Department of Rheumatology and Immunology, Inselspital, Bern University Hospital.
Rheumatology (Oxford) ; 60(11): 5052-5059, 2021 11 03.
Article em En | MEDLINE | ID: mdl-34117737
ABSTRACT

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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arterite de Células Gigantes / Anticorpos Monoclonais Humanizados / Glucocorticoides Tipo de estudo: Diagnostic_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arterite de Células Gigantes / Anticorpos Monoclonais Humanizados / Glucocorticoides Tipo de estudo: Diagnostic_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article