Improvement of asymmetric thyroid eye disease with teprotumumab
PurposeTeprotumumab, 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 pa...
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Veröffentlicht in: | British journal of ophthalmology 2022-06, Vol.106 (6), p.755-759 |
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description | PurposeTeprotumumab, 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.MethodsIn 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.ResultsFrom 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.ConclusionThe 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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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.MethodsIn 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.ResultsFrom 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.ConclusionThe findings in this study suggest the differential impact of teprotumumab on orbits that are clinically more affected by TED, suggesting that teprotumumab reduces asymmetry.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjophthalmol-2020-318314</identifier><identifier>PMID: 33579690</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Asymmetry ; Clinical Science ; Diplopia ; eye (globe) ; Eye diseases ; eye lids ; Graves disease ; Hyaluronic acid ; immunology ; Inflammation ; Insulin-like growth factors ; Monoclonal antibodies ; orbit ; Pathogenesis ; pathology ; Patients ; Statistical analysis ; Thyroid gland</subject><ispartof>British journal of ophthalmology, 2022-06, Vol.106 (6), p.755-759</ispartof><rights>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.</rights><rights>Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2022 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. http://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/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>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. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b537t-596e4ddadb731d05e351943b262dddde0e4a04d5e30a42465b3a2a5b898f503</citedby><cites>FETCH-LOGICAL-b537t-596e4ddadb731d05e351943b262dddde0e4a04d5e30a42465b3a2a5b898f503</cites><orcidid>0000-0003-4479-3033</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132868/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132868/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33579690$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ugradar, Shoaib</creatorcontrib><creatorcontrib>Wang, Yao</creatorcontrib><creatorcontrib>Mester, Tunde</creatorcontrib><creatorcontrib>Kahaly, George J</creatorcontrib><creatorcontrib>Douglas, Raymond</creatorcontrib><title>Improvement of asymmetric thyroid eye disease with teprotumumab</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><addtitle>Br J Ophthalmol</addtitle><description>PurposeTeprotumumab, 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.MethodsIn 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.ResultsFrom 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.ConclusionThe findings in this study suggest the differential impact of teprotumumab on orbits that are clinically more affected by TED, suggesting that teprotumumab reduces asymmetry.</description><subject>Asymmetry</subject><subject>Clinical Science</subject><subject>Diplopia</subject><subject>eye (globe)</subject><subject>Eye diseases</subject><subject>eye lids</subject><subject>Graves disease</subject><subject>Hyaluronic acid</subject><subject>immunology</subject><subject>Inflammation</subject><subject>Insulin-like growth factors</subject><subject>Monoclonal antibodies</subject><subject>orbit</subject><subject>Pathogenesis</subject><subject>pathology</subject><subject>Patients</subject><subject>Statistical analysis</subject><subject>Thyroid gland</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>ACMMV</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqVkUtrGzEUhUVpaJykfyEMdNPNJHrPaNNSQh4GQxbJXkjWdWbMyHIljYv_fRWcuE43IdoIXX3ncC4HoYrgC0KYvLTLsO5yZwYfhppiimtGWkb4JzQhXLZl1KjPaIIxbmpCJDlGJykty5NK0nxBx4yJRkmFJ-jn1K9j2ICHVa7CojJp6z3k2M-r3G1j6F0FW6hcn8AkqP70uasyFEke_eiNPUNHCzMk-Ppyn6KHm-vHq7t6dn87vfo1q61gTa6FksCdM842jDgsgAmiOLNUUlcOYOAGc1fm2HDKpbDMUCNsq9qFwOwU_di5rkfrwc1L2GgGvY69N3Grg-n1259V3-mnsNGKMNrKthh8fzGI4fcIKWvfpzkMg1lBGJOmvFVUCsZoQb_9hy7DGFdlOU2lbChTGJNCtTtqHkNKERb7MATr5470YUf6uSO966hIzw-X2QtfSykA2wHWLz9iy_-p9pHflf0FFQ-0WQ</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Ugradar, Shoaib</creator><creator>Wang, Yao</creator><creator>Mester, Tunde</creator><creator>Kahaly, George J</creator><creator>Douglas, Raymond</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4479-3033</orcidid></search><sort><creationdate>20220601</creationdate><title>Improvement of asymmetric thyroid eye disease with teprotumumab</title><author>Ugradar, Shoaib ; Wang, Yao ; Mester, Tunde ; Kahaly, George J ; Douglas, Raymond</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b537t-596e4ddadb731d05e351943b262dddde0e4a04d5e30a42465b3a2a5b898f503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Asymmetry</topic><topic>Clinical Science</topic><topic>Diplopia</topic><topic>eye (globe)</topic><topic>Eye diseases</topic><topic>eye lids</topic><topic>Graves disease</topic><topic>Hyaluronic acid</topic><topic>immunology</topic><topic>Inflammation</topic><topic>Insulin-like growth factors</topic><topic>Monoclonal antibodies</topic><topic>orbit</topic><topic>Pathogenesis</topic><topic>pathology</topic><topic>Patients</topic><topic>Statistical analysis</topic><topic>Thyroid gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ugradar, Shoaib</creatorcontrib><creatorcontrib>Wang, Yao</creatorcontrib><creatorcontrib>Mester, Tunde</creatorcontrib><creatorcontrib>Kahaly, George J</creatorcontrib><creatorcontrib>Douglas, Raymond</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ugradar, Shoaib</au><au>Wang, Yao</au><au>Mester, Tunde</au><au>Kahaly, George J</au><au>Douglas, Raymond</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improvement of asymmetric thyroid eye disease with teprotumumab</atitle><jtitle>British journal of ophthalmology</jtitle><stitle>Br J Ophthalmol</stitle><addtitle>Br J Ophthalmol</addtitle><date>2022-06-01</date><risdate>2022</risdate><volume>106</volume><issue>6</issue><spage>755</spage><epage>759</epage><pages>755-759</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><abstract>PurposeTeprotumumab, 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.MethodsIn 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.ResultsFrom 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.ConclusionThe findings in this study suggest the differential impact of teprotumumab on orbits that are clinically more affected by TED, suggesting that teprotumumab reduces asymmetry.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>33579690</pmid><doi>10.1136/bjophthalmol-2020-318314</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-4479-3033</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Asymmetry Clinical Science Diplopia eye (globe) Eye diseases eye lids Graves disease Hyaluronic acid immunology Inflammation Insulin-like growth factors Monoclonal antibodies orbit Pathogenesis pathology Patients Statistical analysis Thyroid gland |
title | Improvement of asymmetric thyroid eye disease with teprotumumab |
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