Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development

Acute myeloid leukemia (AML) is a genetically heterogeneous malignancy comprised of various cytogenetic and molecular abnormalities that has notoriously been difficult to treat with an overall poor prognosis. For decades, treatment options were limited to either intensive chemotherapy with anthracyc...

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Main Authors: Michele Stanchina, Deborah Soong, Binbin Zheng-Lin, Justin M. Watts, Justin Taylor
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/11/3225
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author Michele Stanchina
Deborah Soong
Binbin Zheng-Lin
Justin M. Watts
Justin Taylor
author_facet Michele Stanchina
Deborah Soong
Binbin Zheng-Lin
Justin M. Watts
Justin Taylor
author_sort Michele Stanchina
collection DOAJ
description Acute myeloid leukemia (AML) is a genetically heterogeneous malignancy comprised of various cytogenetic and molecular abnormalities that has notoriously been difficult to treat with an overall poor prognosis. For decades, treatment options were limited to either intensive chemotherapy with anthracycline and cytarabine-based regimens (7 + 3) or lower intensity regimens including hypomethylating agents or low dose cytarabine, followed by either allogeneic stem cell transplant or consolidation chemotherapy. Fortunately, with the influx of rapidly evolving molecular technologies and new genetic understanding, the treatment landscape for AML has dramatically changed. Advances in the formulation and delivery of 7 + 3 with liposomal cytarabine and daunorubicin (Vyxeos) have improved overall survival in secondary AML. Increased understanding of the genetic underpinnings of AML has led to targeting actionable mutations such as <i>FLT3</i>, <i>IDH1/2</i> and <i>TP53</i>, and BCL2 or hedgehog pathways in more frail populations. Antibody drug conjugates have resurfaced in the AML landscape and there have been numerous advances utilizing immunotherapies including immune checkpoint inhibitors, antibody-drug conjugates, bispecific T cell engager antibodies, chimeric antigen receptor (CAR)-T therapy and the development of AML vaccines. While there are dozens of ongoing studies and new drugs in the pipeline, this paper serves as a review of the advances achieved in the treatment of AML in the last several years and the most promising future avenues of advancement
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spelling doaj.art-0d41531b0a9540bbb6cb301d3e70c7d22023-11-20T19:26:20ZengMDPI AGCancers2072-66942020-11-011211322510.3390/cancers12113225Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in DevelopmentMichele Stanchina0Deborah Soong1Binbin Zheng-Lin2Justin M. Watts3Justin Taylor4Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USADepartment of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USADepartment of Medicine, Icahn School of Medicine Mount Sinai West-Morningside, New York, NY 10025, USADivision of Hematology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USADivision of Hematology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USAAcute myeloid leukemia (AML) is a genetically heterogeneous malignancy comprised of various cytogenetic and molecular abnormalities that has notoriously been difficult to treat with an overall poor prognosis. For decades, treatment options were limited to either intensive chemotherapy with anthracycline and cytarabine-based regimens (7 + 3) or lower intensity regimens including hypomethylating agents or low dose cytarabine, followed by either allogeneic stem cell transplant or consolidation chemotherapy. Fortunately, with the influx of rapidly evolving molecular technologies and new genetic understanding, the treatment landscape for AML has dramatically changed. Advances in the formulation and delivery of 7 + 3 with liposomal cytarabine and daunorubicin (Vyxeos) have improved overall survival in secondary AML. Increased understanding of the genetic underpinnings of AML has led to targeting actionable mutations such as <i>FLT3</i>, <i>IDH1/2</i> and <i>TP53</i>, and BCL2 or hedgehog pathways in more frail populations. Antibody drug conjugates have resurfaced in the AML landscape and there have been numerous advances utilizing immunotherapies including immune checkpoint inhibitors, antibody-drug conjugates, bispecific T cell engager antibodies, chimeric antigen receptor (CAR)-T therapy and the development of AML vaccines. While there are dozens of ongoing studies and new drugs in the pipeline, this paper serves as a review of the advances achieved in the treatment of AML in the last several years and the most promising future avenues of advancementhttps://www.mdpi.com/2072-6694/12/11/3225novel therapeutics AMLFLT3IDH1/2CD33BCL2CD47
spellingShingle Michele Stanchina
Deborah Soong
Binbin Zheng-Lin
Justin M. Watts
Justin Taylor
Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development
Cancers
novel therapeutics AML
FLT3
IDH1/2
CD33
BCL2
CD47
title Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development
title_full Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development
title_fullStr Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development
title_full_unstemmed Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development
title_short Advances in Acute Myeloid Leukemia: Recently Approved Therapies and Drugs in Development
title_sort advances in acute myeloid leukemia recently approved therapies and drugs in development
topic novel therapeutics AML
FLT3
IDH1/2
CD33
BCL2
CD47
url https://www.mdpi.com/2072-6694/12/11/3225
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AT binbinzhenglin advancesinacutemyeloidleukemiarecentlyapprovedtherapiesanddrugsindevelopment
AT justinmwatts advancesinacutemyeloidleukemiarecentlyapprovedtherapiesanddrugsindevelopment
AT justintaylor advancesinacutemyeloidleukemiarecentlyapprovedtherapiesanddrugsindevelopment