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Recent drug approvals for acute myeloid leukemia

Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, with an incidence that increases with age, and a generally poor prognosis. The disease is clinically and genetically heterogeneous, and recent advances have improved our understanding of the cytogenetic abnormalities a...

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Autores principales: Lai, Catherine, Doucette, Kimberley, Norsworthy, Kelly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749668/
https://www.ncbi.nlm.nih.gov/pubmed/31533852
http://dx.doi.org/10.1186/s13045-019-0774-x
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author Lai, Catherine
Doucette, Kimberley
Norsworthy, Kelly
author_facet Lai, Catherine
Doucette, Kimberley
Norsworthy, Kelly
author_sort Lai, Catherine
collection PubMed
description Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, with an incidence that increases with age, and a generally poor prognosis. The disease is clinically and genetically heterogeneous, and recent advances have improved our understanding of the cytogenetic abnormalities and molecular mutations, aiding in prognostication and risk stratification. Until recently, however, therapeutic options were mostly limited to cytotoxic chemotherapy. Since 2017, there has been an explosion of newly approved treatment options both nationally and internationally, with the majority of new drugs targeting specific gene mutations and/or pivotal cell survival pathways. In this review article, we will discuss these new agents approved for the treatment of AML within the last 2 years, and will outline the mechanistic features and clinical trials that led to their approvals.
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spelling pubmed-67496682019-09-23 Recent drug approvals for acute myeloid leukemia Lai, Catherine Doucette, Kimberley Norsworthy, Kelly J Hematol Oncol Review Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, with an incidence that increases with age, and a generally poor prognosis. The disease is clinically and genetically heterogeneous, and recent advances have improved our understanding of the cytogenetic abnormalities and molecular mutations, aiding in prognostication and risk stratification. Until recently, however, therapeutic options were mostly limited to cytotoxic chemotherapy. Since 2017, there has been an explosion of newly approved treatment options both nationally and internationally, with the majority of new drugs targeting specific gene mutations and/or pivotal cell survival pathways. In this review article, we will discuss these new agents approved for the treatment of AML within the last 2 years, and will outline the mechanistic features and clinical trials that led to their approvals. BioMed Central 2019-09-18 /pmc/articles/PMC6749668/ /pubmed/31533852 http://dx.doi.org/10.1186/s13045-019-0774-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Lai, Catherine
Doucette, Kimberley
Norsworthy, Kelly
Recent drug approvals for acute myeloid leukemia
title Recent drug approvals for acute myeloid leukemia
title_full Recent drug approvals for acute myeloid leukemia
title_fullStr Recent drug approvals for acute myeloid leukemia
title_full_unstemmed Recent drug approvals for acute myeloid leukemia
title_short Recent drug approvals for acute myeloid leukemia
title_sort recent drug approvals for acute myeloid leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749668/
https://www.ncbi.nlm.nih.gov/pubmed/31533852
http://dx.doi.org/10.1186/s13045-019-0774-x
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