Quizartinib (AC220): a promising option for acute myeloid leukemia

Fang Zhou, Zheng Ge, Baoan ChenDepartment of Hematology and Oncology (Key Department of Jiangsu Medicine), Zhongda Hospital, Medical School, Southeast University, Nanjing, Jiangsu Province, People’s Republic of ChinaAbstract: Quizartinib is an effective therapy for patients with FLT3-ITD a...

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Main Authors: Zhou F, Ge Z, Chen B
Format: Article
Language:English
Published: Dove Medical Press 2019-04-01
Series:Drug Design, Development and Therapy
Subjects:
Online Access:https://www.dovepress.com/quizartinib-ac220-a-promising-option-for-acute-myeloid-leukemia-peer-reviewed-article-DDDT
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author Zhou F
Ge Z
Chen B
author_facet Zhou F
Ge Z
Chen B
author_sort Zhou F
collection DOAJ
description Fang Zhou, Zheng Ge, Baoan ChenDepartment of Hematology and Oncology (Key Department of Jiangsu Medicine), Zhongda Hospital, Medical School, Southeast University, Nanjing, Jiangsu Province, People’s Republic of ChinaAbstract: Quizartinib is an effective therapy for patients with FLT3-ITD acute myeloid leukemia (AML) by continuing to inhibit the activity of FLT3 gene, leading to apoptosis of tumor cells. Multiple clinical trials have proved that it is effective in relapsed or refractory AML with an FLT3-ITD mutation. In this review, we focus on the characteristics of FLT3/ITD mutations, the mechanism and pharmacokinetics of quizartinib, and the mechanisms of resistance to quizartinib. We also summarize clinical experiences and adverse effects with quizartinib and recommend crucial approaches of quizartinib in the therapy of patients with newly diagnosed AML and patients with relapsed/refractory AML, particularly those with FLT3-ITD mutation. Quizartinib presents its advantages as a very promising agent in the treatment of AML, especially in patients with FLT3-ITD mutations. FLT3/ITD mutation can lead to constitutive autophosphorylation of FLT3 and activation of its downstream effectors including RAS/RAF/MEK, MAPK/ERK, PI3K/AKT/mTOR and JAK/STAT5 signal pathways, while Quizartinib can inhibit these downstream pathways through specific FLT3 inhibition. Quizartinib has received US Food and Drug Administration breakthrough therapy designation in patients with relapsed/refractory FLT3-ITD AML based on clinical trials. A larger sample of clinical trials are needed to verify its safety and efficacy, and the efficacy of quizartinib combined with chemotherapy or allogeneic hematopoietic cell transplantation should also be estimated in clinical trials. Meanwhile, for the side effects of quizartinib, further studies are needed to find a way to reduce its toxicity.Keywords: quizartinib, FLT3 inhibitor, FLT3-ITD mutation, AML, clinical trials, targeted therapy
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spelling doaj.art-086b621df0e848c8a399913e338323242022-12-22T00:55:14ZengDove Medical PressDrug Design, Development and Therapy1177-88812019-04-01Volume 131117112544985Quizartinib (AC220): a promising option for acute myeloid leukemiaZhou FGe ZChen BFang Zhou, Zheng Ge, Baoan ChenDepartment of Hematology and Oncology (Key Department of Jiangsu Medicine), Zhongda Hospital, Medical School, Southeast University, Nanjing, Jiangsu Province, People’s Republic of ChinaAbstract: Quizartinib is an effective therapy for patients with FLT3-ITD acute myeloid leukemia (AML) by continuing to inhibit the activity of FLT3 gene, leading to apoptosis of tumor cells. Multiple clinical trials have proved that it is effective in relapsed or refractory AML with an FLT3-ITD mutation. In this review, we focus on the characteristics of FLT3/ITD mutations, the mechanism and pharmacokinetics of quizartinib, and the mechanisms of resistance to quizartinib. We also summarize clinical experiences and adverse effects with quizartinib and recommend crucial approaches of quizartinib in the therapy of patients with newly diagnosed AML and patients with relapsed/refractory AML, particularly those with FLT3-ITD mutation. Quizartinib presents its advantages as a very promising agent in the treatment of AML, especially in patients with FLT3-ITD mutations. FLT3/ITD mutation can lead to constitutive autophosphorylation of FLT3 and activation of its downstream effectors including RAS/RAF/MEK, MAPK/ERK, PI3K/AKT/mTOR and JAK/STAT5 signal pathways, while Quizartinib can inhibit these downstream pathways through specific FLT3 inhibition. Quizartinib has received US Food and Drug Administration breakthrough therapy designation in patients with relapsed/refractory FLT3-ITD AML based on clinical trials. A larger sample of clinical trials are needed to verify its safety and efficacy, and the efficacy of quizartinib combined with chemotherapy or allogeneic hematopoietic cell transplantation should also be estimated in clinical trials. Meanwhile, for the side effects of quizartinib, further studies are needed to find a way to reduce its toxicity.Keywords: quizartinib, FLT3 inhibitor, FLT3-ITD mutation, AML, clinical trials, targeted therapyhttps://www.dovepress.com/quizartinib-ac220-a-promising-option-for-acute-myeloid-leukemia-peer-reviewed-article-DDDTQuizartinibFLT3 inhibitorFLT3-ITD mutationAMLClinical tricalsTargeted therapy
spellingShingle Zhou F
Ge Z
Chen B
Quizartinib (AC220): a promising option for acute myeloid leukemia
Drug Design, Development and Therapy
Quizartinib
FLT3 inhibitor
FLT3-ITD mutation
AML
Clinical tricals
Targeted therapy
title Quizartinib (AC220): a promising option for acute myeloid leukemia
title_full Quizartinib (AC220): a promising option for acute myeloid leukemia
title_fullStr Quizartinib (AC220): a promising option for acute myeloid leukemia
title_full_unstemmed Quizartinib (AC220): a promising option for acute myeloid leukemia
title_short Quizartinib (AC220): a promising option for acute myeloid leukemia
title_sort quizartinib ac220 a promising option for acute myeloid leukemia
topic Quizartinib
FLT3 inhibitor
FLT3-ITD mutation
AML
Clinical tricals
Targeted therapy
url https://www.dovepress.com/quizartinib-ac220-a-promising-option-for-acute-myeloid-leukemia-peer-reviewed-article-DDDT
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