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Novel Agents for Acute Myeloid Leukemia

Acute myeloid leukemia (AML) is a complex hematological disease characterized by genetic and clinical heterogeneity. Recent advances in the understanding of AML pathogenesis have paved the way for the development of new agents targeting specific molecules or mechanisms that contribute to finally mov...

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Autores principales: Luppi, Mario, Fabbiano, Francesco, Visani, Giuseppe, Martinelli, Giovanni, Venditti, Adriano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267447/
https://www.ncbi.nlm.nih.gov/pubmed/30423907
http://dx.doi.org/10.3390/cancers10110429
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author Luppi, Mario
Fabbiano, Francesco
Visani, Giuseppe
Martinelli, Giovanni
Venditti, Adriano
author_facet Luppi, Mario
Fabbiano, Francesco
Visani, Giuseppe
Martinelli, Giovanni
Venditti, Adriano
author_sort Luppi, Mario
collection PubMed
description Acute myeloid leukemia (AML) is a complex hematological disease characterized by genetic and clinical heterogeneity. Recent advances in the understanding of AML pathogenesis have paved the way for the development of new agents targeting specific molecules or mechanisms that contribute to finally move beyond the current standard of care, which is “3 + 7” regimen. In particular, new therapeutic options such as targeted therapies (midostaurin and enasidenib), monoclonal antibodies (gemtuzumab ozogamicin), and a novel liposomal formulation of cytarabine and daunorubicin (CPX-351) have been recently approved, and will be soon available for the treatment of adult patients with AML. In this review, we will present and describe these recently approved drugs as well as selected novel agents against AML that are currently under investigation, and show the most promising results as monotherapy or in combination with chemotherapy. The selection of these emerging treatments is based on the authors’ opinion.
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spelling pubmed-62674472018-12-03 Novel Agents for Acute Myeloid Leukemia Luppi, Mario Fabbiano, Francesco Visani, Giuseppe Martinelli, Giovanni Venditti, Adriano Cancers (Basel) Review Acute myeloid leukemia (AML) is a complex hematological disease characterized by genetic and clinical heterogeneity. Recent advances in the understanding of AML pathogenesis have paved the way for the development of new agents targeting specific molecules or mechanisms that contribute to finally move beyond the current standard of care, which is “3 + 7” regimen. In particular, new therapeutic options such as targeted therapies (midostaurin and enasidenib), monoclonal antibodies (gemtuzumab ozogamicin), and a novel liposomal formulation of cytarabine and daunorubicin (CPX-351) have been recently approved, and will be soon available for the treatment of adult patients with AML. In this review, we will present and describe these recently approved drugs as well as selected novel agents against AML that are currently under investigation, and show the most promising results as monotherapy or in combination with chemotherapy. The selection of these emerging treatments is based on the authors’ opinion. MDPI 2018-11-09 /pmc/articles/PMC6267447/ /pubmed/30423907 http://dx.doi.org/10.3390/cancers10110429 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Luppi, Mario
Fabbiano, Francesco
Visani, Giuseppe
Martinelli, Giovanni
Venditti, Adriano
Novel Agents for Acute Myeloid Leukemia
title Novel Agents for Acute Myeloid Leukemia
title_full Novel Agents for Acute Myeloid Leukemia
title_fullStr Novel Agents for Acute Myeloid Leukemia
title_full_unstemmed Novel Agents for Acute Myeloid Leukemia
title_short Novel Agents for Acute Myeloid Leukemia
title_sort novel agents for acute myeloid leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267447/
https://www.ncbi.nlm.nih.gov/pubmed/30423907
http://dx.doi.org/10.3390/cancers10110429
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