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Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor
Sickle cell disease, despite its recognition as a severely debilitating genetic condition affecting hundreds of thousands of neonates throughout the world each year, was not a target of pharmaceutical research focus for most of its 100-year existence in the medical consciousness. This has changed in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983433/ https://www.ncbi.nlm.nih.gov/pubmed/33796238 http://dx.doi.org/10.1177/20406207211001136 |
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author | Glaros, Alexander K. Razvi, Reza Shah, Nirmish Zaidi, Ahmar U. |
author_facet | Glaros, Alexander K. Razvi, Reza Shah, Nirmish Zaidi, Ahmar U. |
author_sort | Glaros, Alexander K. |
collection | PubMed |
description | Sickle cell disease, despite its recognition as a severely debilitating genetic condition affecting hundreds of thousands of neonates throughout the world each year, was not a target of pharmaceutical research focus for most of its 100-year existence in the medical consciousness. This has changed in recent years as many novel therapeutics are currently under investigation, with three new disease-modifying drugs achieving FDA approval in the last 4 years. One of these drugs, voxelotor, is especially encouraging as an inhibitor of sickling for its ability to safely improve the chronic hemolytic anemia of sickle cell disease. This was demonstrated during all clinical phases of investigation by an average improvement in hemoglobin of greater than 1 g/dL, as well as statistically significant improvements in established markers of hemolysis. While anemia itself represents a potential cause of morbidity, it is more importantly a marker of the hemolysis known to cause the long-term vascular and organ damage that makes sickle cell disease so debilitating and frequently fatal early in life. Given the recency of the approval, there has not been sufficient long-term follow-up to demonstrate improvement in the chronic sequelae of sickle cell disease as a result of voxelotor-induced improvements in hemolytic anemia. There is hope, however, based on the experience with hydroxyurea improving morbidity and mortality via reductions in sickling and improved rheology, that voxelotor may have similar long-term benefits by positively manipulating the kinetics of hemoglobin polymerization. This review aims to summarize the targeted pathobiology of sickle cell disease, the mechanism of action of voxelotor, and the safety and efficacy data from preclinical to late clinical stage investigations of this long-awaited medication, in the hopes of better informing the decision-making process behind prescribing or not prescribing it for patients in need of intervention. |
format | Online Article Text |
id | pubmed-7983433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79834332021-03-31 Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor Glaros, Alexander K. Razvi, Reza Shah, Nirmish Zaidi, Ahmar U. Ther Adv Hematol Review Article Sickle cell disease, despite its recognition as a severely debilitating genetic condition affecting hundreds of thousands of neonates throughout the world each year, was not a target of pharmaceutical research focus for most of its 100-year existence in the medical consciousness. This has changed in recent years as many novel therapeutics are currently under investigation, with three new disease-modifying drugs achieving FDA approval in the last 4 years. One of these drugs, voxelotor, is especially encouraging as an inhibitor of sickling for its ability to safely improve the chronic hemolytic anemia of sickle cell disease. This was demonstrated during all clinical phases of investigation by an average improvement in hemoglobin of greater than 1 g/dL, as well as statistically significant improvements in established markers of hemolysis. While anemia itself represents a potential cause of morbidity, it is more importantly a marker of the hemolysis known to cause the long-term vascular and organ damage that makes sickle cell disease so debilitating and frequently fatal early in life. Given the recency of the approval, there has not been sufficient long-term follow-up to demonstrate improvement in the chronic sequelae of sickle cell disease as a result of voxelotor-induced improvements in hemolytic anemia. There is hope, however, based on the experience with hydroxyurea improving morbidity and mortality via reductions in sickling and improved rheology, that voxelotor may have similar long-term benefits by positively manipulating the kinetics of hemoglobin polymerization. This review aims to summarize the targeted pathobiology of sickle cell disease, the mechanism of action of voxelotor, and the safety and efficacy data from preclinical to late clinical stage investigations of this long-awaited medication, in the hopes of better informing the decision-making process behind prescribing or not prescribing it for patients in need of intervention. SAGE Publications 2021-03-19 /pmc/articles/PMC7983433/ /pubmed/33796238 http://dx.doi.org/10.1177/20406207211001136 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Article Glaros, Alexander K. Razvi, Reza Shah, Nirmish Zaidi, Ahmar U. Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
title | Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
title_full | Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
title_fullStr | Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
title_full_unstemmed | Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
title_short | Voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
title_sort | voxelotor: alteration of sickle cell disease pathophysiology by a first-in-class polymerization inhibitor |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983433/ https://www.ncbi.nlm.nih.gov/pubmed/33796238 http://dx.doi.org/10.1177/20406207211001136 |
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