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Improvement of asymmetric thyroid eye disease with teprotumumab

PURPOSE: Teprotumumab, a specific blocking antibody to the insulin like growth factor 1 receptor, significantly reduced proptosis in patients with thyroid eye disease (TED) in recent clinical trials. Given its specificity, we expect it to demonstrate greater efficacy on the worse affected orbit, in...

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Autores principales: Ugradar, Shoaib, Wang, Yao, Mester, Tunde, Kahaly, George J, Douglas, Raymond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132868/
https://www.ncbi.nlm.nih.gov/pubmed/33579690
http://dx.doi.org/10.1136/bjophthalmol-2020-318314
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author Ugradar, Shoaib
Wang, Yao
Mester, Tunde
Kahaly, George J
Douglas, Raymond
author_facet Ugradar, Shoaib
Wang, Yao
Mester, Tunde
Kahaly, George J
Douglas, Raymond
author_sort Ugradar, Shoaib
collection PubMed
description PURPOSE: Teprotumumab, a specific blocking antibody to the insulin like growth factor 1 receptor, significantly reduced proptosis in patients with thyroid eye disease (TED) in recent clinical trials. Given its specificity, we expect it to demonstrate greater efficacy on the worse affected orbit, in patients with asymmetric TED. Herein, we investigate the differential impact of teprotumumab on the orbits of such patients. METHODS: In this pooled analysis of patients who were enrolled in the recent phase 2 (NCT01868997) and phase 3 (NCT03298867) trials, all patients with asymmetric TED (difference in exophthalmometry of ≥3 mm) were screened for eligibility. The primary outcomes of the trials, proptosis, diplopia and Clinical Activity Score (CAS) response, were evaluated in both orbits of patients who had received treatment or placebo, to examine the differential response from baseline to week 24. RESULTS: From a pooled group of 84 patients randomised to receive teprotumumab and 87 randomised to placebo, 10 (12%) and 12 (14%), respectively, met the inclusion criteria. The teprotumumab-treated patients demonstrated significant reductions in proptosis, CAS and diplopia in both orbits of each patient and this was not seen with placebo. The reduction in proptosis and CAS was significantly greater in the worse affected orbit, improving symmetry. In the placebo arm, while the mean CAS in the study eye reduced over time, proptosis and diplopia did not change in either orbit. CONCLUSION: The findings in this study suggest the differential impact of teprotumumab on orbits that are clinically more affected by TED, suggesting that teprotumumab reduces asymmetry.
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spelling pubmed-91328682022-06-10 Improvement of asymmetric thyroid eye disease with teprotumumab Ugradar, Shoaib Wang, Yao Mester, Tunde Kahaly, George J Douglas, Raymond Br J Ophthalmol Clinical Science PURPOSE: Teprotumumab, a specific blocking antibody to the insulin like growth factor 1 receptor, significantly reduced proptosis in patients with thyroid eye disease (TED) in recent clinical trials. Given its specificity, we expect it to demonstrate greater efficacy on the worse affected orbit, in patients with asymmetric TED. Herein, we investigate the differential impact of teprotumumab on the orbits of such patients. METHODS: In this pooled analysis of patients who were enrolled in the recent phase 2 (NCT01868997) and phase 3 (NCT03298867) trials, all patients with asymmetric TED (difference in exophthalmometry of ≥3 mm) were screened for eligibility. The primary outcomes of the trials, proptosis, diplopia and Clinical Activity Score (CAS) response, were evaluated in both orbits of patients who had received treatment or placebo, to examine the differential response from baseline to week 24. RESULTS: From a pooled group of 84 patients randomised to receive teprotumumab and 87 randomised to placebo, 10 (12%) and 12 (14%), respectively, met the inclusion criteria. The teprotumumab-treated patients demonstrated significant reductions in proptosis, CAS and diplopia in both orbits of each patient and this was not seen with placebo. The reduction in proptosis and CAS was significantly greater in the worse affected orbit, improving symmetry. In the placebo arm, while the mean CAS in the study eye reduced over time, proptosis and diplopia did not change in either orbit. CONCLUSION: The findings in this study suggest the differential impact of teprotumumab on orbits that are clinically more affected by TED, suggesting that teprotumumab reduces asymmetry. BMJ Publishing Group 2022-06 2021-02-12 /pmc/articles/PMC9132868/ /pubmed/33579690 http://dx.doi.org/10.1136/bjophthalmol-2020-318314 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Clinical Science
Ugradar, Shoaib
Wang, Yao
Mester, Tunde
Kahaly, George J
Douglas, Raymond
Improvement of asymmetric thyroid eye disease with teprotumumab
title Improvement of asymmetric thyroid eye disease with teprotumumab
title_full Improvement of asymmetric thyroid eye disease with teprotumumab
title_fullStr Improvement of asymmetric thyroid eye disease with teprotumumab
title_full_unstemmed Improvement of asymmetric thyroid eye disease with teprotumumab
title_short Improvement of asymmetric thyroid eye disease with teprotumumab
title_sort improvement of asymmetric thyroid eye disease with teprotumumab
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132868/
https://www.ncbi.nlm.nih.gov/pubmed/33579690
http://dx.doi.org/10.1136/bjophthalmol-2020-318314
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