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Maintenance Therapy in AML

Recent advances in therapeutics coupled with steady improvements in supportive care for patients with acute myeloid leukemia (AML) have led to improved outcomes. Despite these advances, even in patients that achieve a complete remission with initial therapy high rates of relapse remain a clinical di...

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Detalles Bibliográficos
Autores principales: Reville, Patrick K., Kadia, Tapan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884813/
https://www.ncbi.nlm.nih.gov/pubmed/33604298
http://dx.doi.org/10.3389/fonc.2020.619085
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author Reville, Patrick K.
Kadia, Tapan M.
author_facet Reville, Patrick K.
Kadia, Tapan M.
author_sort Reville, Patrick K.
collection PubMed
description Recent advances in therapeutics coupled with steady improvements in supportive care for patients with acute myeloid leukemia (AML) have led to improved outcomes. Despite these advances, even in patients that achieve a complete remission with initial therapy high rates of relapse remain a clinical dilemma. For decades, investigators have attempted strategies of maintenance therapy to prolong both remission duration and overall survival in patients with AML. These approaches have included cytotoxic chemotherapy, immunotherapy, hypomethylating agents, and targeted small molecule therapy. Overall, the evidence in favor of maintenance therapy is limited. Recent strategies, especially with hypomethylating agents have begun to show promise as maintenance therapy in improving clinical outcomes. Ongoing and future studies will continue to elucidate the true role for maintenance therapy options in patients with AML. In this review we summarize prior and ongoing maintenance therapy approaches in AML and highlight some of the most promising strategies.
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spelling pubmed-78848132021-02-17 Maintenance Therapy in AML Reville, Patrick K. Kadia, Tapan M. Front Oncol Oncology Recent advances in therapeutics coupled with steady improvements in supportive care for patients with acute myeloid leukemia (AML) have led to improved outcomes. Despite these advances, even in patients that achieve a complete remission with initial therapy high rates of relapse remain a clinical dilemma. For decades, investigators have attempted strategies of maintenance therapy to prolong both remission duration and overall survival in patients with AML. These approaches have included cytotoxic chemotherapy, immunotherapy, hypomethylating agents, and targeted small molecule therapy. Overall, the evidence in favor of maintenance therapy is limited. Recent strategies, especially with hypomethylating agents have begun to show promise as maintenance therapy in improving clinical outcomes. Ongoing and future studies will continue to elucidate the true role for maintenance therapy options in patients with AML. In this review we summarize prior and ongoing maintenance therapy approaches in AML and highlight some of the most promising strategies. Frontiers Media S.A. 2021-02-02 /pmc/articles/PMC7884813/ /pubmed/33604298 http://dx.doi.org/10.3389/fonc.2020.619085 Text en Copyright © 2021 Reville and Kadia http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Reville, Patrick K.
Kadia, Tapan M.
Maintenance Therapy in AML
title Maintenance Therapy in AML
title_full Maintenance Therapy in AML
title_fullStr Maintenance Therapy in AML
title_full_unstemmed Maintenance Therapy in AML
title_short Maintenance Therapy in AML
title_sort maintenance therapy in aml
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884813/
https://www.ncbi.nlm.nih.gov/pubmed/33604298
http://dx.doi.org/10.3389/fonc.2020.619085
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