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Relapsed or primary refractory AML: moving past MEC and FLAG-ida

Treatment of relapsed and refractory acute myeloid leukemia (AML) is still very challenging, with poor response rates and low chance for cure. This is especially true when treating patients who are elderly, have multiple comorbidities, or who are too unfit for traditional salvage chemotherapy regime...

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Detalles Bibliográficos
Autores principales: Koenig, Kristin, Mims, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams And Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015186/
https://www.ncbi.nlm.nih.gov/pubmed/31904664
http://dx.doi.org/10.1097/MOH.0000000000000561
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author Koenig, Kristin
Mims, Alice
author_facet Koenig, Kristin
Mims, Alice
author_sort Koenig, Kristin
collection PubMed
description Treatment of relapsed and refractory acute myeloid leukemia (AML) is still very challenging, with poor response rates and low chance for cure. This is especially true when treating patients who are elderly, have multiple comorbidities, or who are too unfit for traditional salvage chemotherapy regimens. RECENT FINDINGS: Recently, advances in the treatment of relapsed/refractory AML utilizing novel chemotherapy combinations, hypomethylating, and targeted therapies have shown promising results. SUMMARY: Several early-phase studies with novel targeted therapy combinations have demonstrated encouraging results warranting larger, comparative studies. This has expanded the access of treatment for patients with relapsed/refractory AML who cannot receive traditional salvage chemotherapy. These newer treatments have the potential to outperform traditional chemotherapy as well.
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spelling pubmed-70151862020-03-10 Relapsed or primary refractory AML: moving past MEC and FLAG-ida Koenig, Kristin Mims, Alice Curr Opin Hematol MYELOID DISEASE: Edited by Martin S. Tallman Treatment of relapsed and refractory acute myeloid leukemia (AML) is still very challenging, with poor response rates and low chance for cure. This is especially true when treating patients who are elderly, have multiple comorbidities, or who are too unfit for traditional salvage chemotherapy regimens. RECENT FINDINGS: Recently, advances in the treatment of relapsed/refractory AML utilizing novel chemotherapy combinations, hypomethylating, and targeted therapies have shown promising results. SUMMARY: Several early-phase studies with novel targeted therapy combinations have demonstrated encouraging results warranting larger, comparative studies. This has expanded the access of treatment for patients with relapsed/refractory AML who cannot receive traditional salvage chemotherapy. These newer treatments have the potential to outperform traditional chemotherapy as well. Lippincott Williams And Wilkins 2020-03 2020-01-20 /pmc/articles/PMC7015186/ /pubmed/31904664 http://dx.doi.org/10.1097/MOH.0000000000000561 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle MYELOID DISEASE: Edited by Martin S. Tallman
Koenig, Kristin
Mims, Alice
Relapsed or primary refractory AML: moving past MEC and FLAG-ida
title Relapsed or primary refractory AML: moving past MEC and FLAG-ida
title_full Relapsed or primary refractory AML: moving past MEC and FLAG-ida
title_fullStr Relapsed or primary refractory AML: moving past MEC and FLAG-ida
title_full_unstemmed Relapsed or primary refractory AML: moving past MEC and FLAG-ida
title_short Relapsed or primary refractory AML: moving past MEC and FLAG-ida
title_sort relapsed or primary refractory aml: moving past mec and flag-ida
topic MYELOID DISEASE: Edited by Martin S. Tallman
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015186/
https://www.ncbi.nlm.nih.gov/pubmed/31904664
http://dx.doi.org/10.1097/MOH.0000000000000561
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