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Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema
BACKGROUND: Hereditary angioedema (HAE) is a rare genetic disorder characterized by unpredictable localized episodes of edema, which is frequently managed with long-term prophylactic medications. Until recently, long-term prophylaxis has predominantly required regular intravenous or subcutaneous adm...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501591/ https://www.ncbi.nlm.nih.gov/pubmed/34627358 http://dx.doi.org/10.1186/s13223-021-00603-9 |
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author | Gower, Richard G. Wilber, Mary |
author_facet | Gower, Richard G. Wilber, Mary |
author_sort | Gower, Richard G. |
collection | PubMed |
description | BACKGROUND: Hereditary angioedema (HAE) is a rare genetic disorder characterized by unpredictable localized episodes of edema, which is frequently managed with long-term prophylactic medications. Until recently, long-term prophylaxis has predominantly required regular intravenous or subcutaneous administration, however the recent approval of berotralstat (Orladeyo™) offers an orally administered prophylactic which may be associated with a lower burden of treatment compared to injectable options for some patients. CASE PRESENTATION: This report describes four participants in the APeX-S trial who transitioned from subcutaneously administered lanadelumab (Takhzyro(®)) to daily oral berotralstat for long-term HAE prophylaxis. Lanadelumab dosing continued after berotralstat commencement in all patients and was tapered before discontinuation in three of the four patients. No substantial increases in HAE attack rates were observed after the transition to berotralstat monotherapy. One patient experienced a treatment-related adverse event (dyspepsia), which was mild and self-resolving. CONCLUSIONS: All four patients described in this case series successfully transitioned from lanadelumab to berotralstat monotherapy for long-term prophylaxis without significant complications and without the use of a complex transition protocol. The decision to transition to berotralstat monotherapy and how the transition should be achieved was discussed between patient and physician, ensuring that the comfort and perspectives of the patients were considered during the treatment transition. This report highlights the importance of individualization of HAE management plans to address both the disease and treatment burdens of HAE, and thus to provide the best possible quality of life for each patient. |
format | Online Article Text |
id | pubmed-8501591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85015912021-10-20 Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema Gower, Richard G. Wilber, Mary Allergy Asthma Clin Immunol Case Report BACKGROUND: Hereditary angioedema (HAE) is a rare genetic disorder characterized by unpredictable localized episodes of edema, which is frequently managed with long-term prophylactic medications. Until recently, long-term prophylaxis has predominantly required regular intravenous or subcutaneous administration, however the recent approval of berotralstat (Orladeyo™) offers an orally administered prophylactic which may be associated with a lower burden of treatment compared to injectable options for some patients. CASE PRESENTATION: This report describes four participants in the APeX-S trial who transitioned from subcutaneously administered lanadelumab (Takhzyro(®)) to daily oral berotralstat for long-term HAE prophylaxis. Lanadelumab dosing continued after berotralstat commencement in all patients and was tapered before discontinuation in three of the four patients. No substantial increases in HAE attack rates were observed after the transition to berotralstat monotherapy. One patient experienced a treatment-related adverse event (dyspepsia), which was mild and self-resolving. CONCLUSIONS: All four patients described in this case series successfully transitioned from lanadelumab to berotralstat monotherapy for long-term prophylaxis without significant complications and without the use of a complex transition protocol. The decision to transition to berotralstat monotherapy and how the transition should be achieved was discussed between patient and physician, ensuring that the comfort and perspectives of the patients were considered during the treatment transition. This report highlights the importance of individualization of HAE management plans to address both the disease and treatment burdens of HAE, and thus to provide the best possible quality of life for each patient. BioMed Central 2021-10-09 /pmc/articles/PMC8501591/ /pubmed/34627358 http://dx.doi.org/10.1186/s13223-021-00603-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Gower, Richard G. Wilber, Mary Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
title | Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
title_full | Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
title_fullStr | Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
title_full_unstemmed | Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
title_short | Considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
title_sort | considerations for transition from subcutaneous to oral prophylaxis in the treatment of hereditary angioedema |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501591/ https://www.ncbi.nlm.nih.gov/pubmed/34627358 http://dx.doi.org/10.1186/s13223-021-00603-9 |
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