The position of monoclonal antibodies and small molecules in the treatment of thyroid orbitopathy
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An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
Mariusz Nowak1, Wojciech Nowak2, Bogdan Marek3
1Pathophysiology Division, Department of Pathophysiology and Endocrinology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Poland. nowak-mar@wp.pl.
Abstract:
Since the European Thyroid Association guidelines for the management of thyroid orbitopathy (TO) were published in 2016, a number of randomised clinical trials (RCTs) investigating the use of biologic drugs for the treatment of moderate to severe and active TO have been published. Therefore, new recommendations for its treatment were developed and published in 2021. Treatment of active TO includes 2 types of immunosuppressive agents: non-specific and specific. Specific immunosuppressive agents used to treat TO include adalimumab (ADA), infliximab (IFX), etanercept (ETA), rituximab (RTX), tocilizumab (TCZ), teprotumumab (TEP), and batoclimab (BAT). In the manuscript, we present a review of the literature on RCTs, retrospective studies, and case reports on their use in the treatment of TO. The authors emphasise the beneficial effects of TEP, indicating, however, the lack of data on its long-term efficacy and safety and the lack of head-to-head comparison with i.v. glucocorticosteroids and its huge limitation is also the high price of the drug. TCZ is a therapeutic option for glucocorticosteroid-resistant TO and should be considered for second-line treatment (due to the cost of treatment, among other reasons) or first-line treatment in patients with contraindications to i.v. glucocorticosteroids. Given its side-effect profile, especially some risk of optic nerve neuropathy (DON), RTX is considered by the authors as a second- or even third-line treatment option. The current 2021 European Group on Graves' Orbitopathy (EUGOGO) recommendations include RTX, TCZ, and TEP among the second-line drugs for the treatment of moderate to severe and active TO. BAT is under clinical trials. Given the numerous advantages of biologic drugs over glucocorticosteroids, further RCTs are indicated to confirm their possible place also as first-line treatment in TO.
Insights
New biologic drugs offer promising treatments for moderate to severe thyroid orbitopathy (TO). While effective, further research is needed to confirm their long-term safety and optimal use compared to existing therapies.
Area of Science:
- Ophthalmology
- Endocrinology
- Immunology
Background:
- Thyroid orbitopathy (TO) management guidelines evolved in 2021 following new randomized clinical trials (RCTs).
- Treatment for active TO now includes specific immunosuppressive biologic agents.
- Several biologic drugs are available, including adalimumab, infliximab, etanercept, rituximab, tocilizumab, teprotumumab, and batoclimab.
Purpose of the Study:
- To review the literature on the efficacy and safety of biologic drugs for moderate to severe active thyroid orbitopathy.
- To compare the current recommendations for biologic drug use in TO treatment.
- To identify areas for future research in biologic therapy for TO.
Main Methods:
- Literature review of randomized clinical trials (RCTs), retrospective studies, and case reports.
- Analysis of data on the use of specific immunosuppressive agents for TO treatment.
- Evaluation of current European Group on Graves' Orbitopathy (EUGOGO) recommendations.
Main Results:
- Teprotumumab shows beneficial effects but lacks long-term data and head-to-head comparisons; its high cost is a limitation.
- Tocilizumab is a viable option for glucocorticosteroid-resistant TO, suitable for second-line or first-line treatment in specific cases.
- Rituximab is considered a second- or third-line option due to potential side effects like optic nerve neuropathy.
- Current EUGOGO guidelines recommend rituximab, tocilizumab, and teprotumumab as second-line treatments for moderate to severe active TO.
Conclusions:
- Biologic drugs offer advantages over glucocorticosteroids for TO treatment.
- Further RCTs are needed to establish biologics as first-line therapy for TO.
- Long-term efficacy and safety data for newer agents like teprotumumab require further investigation.
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