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Efficiency and Safety of Tocilizumab for the Treatment of Thyroid Eye Disease: A Systematic Review.
Duarte, Ana F; Xavier, Naiara F; Sales Sanz, Marco; Cruz, Antonio A V.
Afiliación
  • Duarte AF; Department of Ophthalmology, Centro Hospitalar Universitario Lisboa Central, Lisbon, Portugal.
  • Xavier NF; Department of Ophthalmology, Cuf Descobertas Hospital, Lisbon, Portugal.
  • Sales Sanz M; Department of Ophthalmology, School of Medicine of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • Cruz AAV; Department of Ophthalmology, Hospital Universitario Ramon y Cajal, Madrid, Spain.
Ophthalmic Plast Reconstr Surg ; 40(4): 367-373, 2024.
Article en En | MEDLINE | ID: mdl-38215463
ABSTRACT

PURPOSE:

To review existing literature concerning the effectiveness and safety of tocilizumab (TCZ) for managing thyroid eye disease.

METHODS:

A systematic search was conducted across the PubMed and Embase databases to identify studies on TCZ therapy, from inception to May 2023. The search included the keywords "Graves orbitopathy," "thyroid ophthalmopathy," "thyroid eye disease," "thyroid-associated orbitopathy," "thyroid-associated ophthalmopathy," "Graves ophthalmopathy," "endocrine ophthalmopathy," and "Tocilizumab." Only articles written in English, Spanish, or French were considered.

RESULTS:

Among the 1,013 articles initially screened, a total of 29 fulfilled the eligibility criteria and were selected. Most studies were case reports or case series, and only one randomized clinical trial was found. TCZ has been used mainly in glucocorticoid-resistant or relapsing cases, with a dosage ranging from 4 or 8 mg/kg every 4 weeks when intravenous or a weekly subcutaneous dose of 162 mg. Treatment duration is usually adjusted to the clinical response. TCZ is mostly effective in reducing inflammatory signs during the active phase of thyroid eye disease, with an improvement of at least 3 points in clinical activity score and an overall relapsing rate of 8.2%. Numerous studies have shown marked reductions in proptosis; although the only available randomized controlled trial reported a nonstatistically significant improvement 6 months after treatment, a recent meta-analysis indicated that TCZ seems to be the most effective treatment for reducing proptosis. No severe side effects related to intravenous or subcutaneous TCZ administration were reported.

DISCUSSION:

Despite these promising findings, randomized clinical trials to directly compare the efficacy and safety of TCZ and other currently available therapeutic options are needed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oftalmopatía de Graves / Anticuerpos Monoclonales Humanizados Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Ophthalmic Plast Reconstr Surg Asunto de la revista: OFTALMOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Portugal

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oftalmopatía de Graves / Anticuerpos Monoclonales Humanizados Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Ophthalmic Plast Reconstr Surg Asunto de la revista: OFTALMOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Portugal