Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,003,479 papers from all fields of science
Search
Sign In
Create Free Account
AC220
Known as:
AC-220
, AC010220
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Quizartinib
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Glutaminase inhibition improves FLT3 inhibitor therapy for acute myeloid leukemia.
M. Gregory
,
T. Nemkov
,
+4 authors
J. DeGregori
Experimental Hematology
2017
Corpus ID: 3586430
Highly Cited
2015
Highly Cited
2015
Receptor tyrosine kinase Axl is required for resistance of leukemic cells to FLT3-targeted therapy in acute myeloid leukemia
Il-kyoo Park
,
B. Mundy-Bosse
,
+6 authors
M. Caligiuri
Leukemia
2015
Corpus ID: 28071109
In acute myeloid leukemia (AML), about 25–30% of patients harbor a constitutively active receptor tyrosine kinase (RTK) FLT3…
Expand
2014
2014
Clinically relevant doses of FLT3-kinase inhibitors quizartinib and midostaurin do not impair T-cell reactivity and function
D. Wolleschak
,
T. S. Mack
,
+15 authors
F. Heidel
Haematologica
2014
Corpus ID: 1776033
The vast majority of acute myeloid leukemia (AML) patients harboring an FLT3-ITD mutation experience relapse within a short…
Expand
2014
2014
Final results of a randomized phase 2 study showing the clinical benefit of quizartinib (AC220) in patients with FLT3-ITD positive relapsed or refractory acute myeloid leukemia.
G. Schiller
,
M. Tallman
,
+9 authors
J. Cortes
2014
Corpus ID: 79851547
7100 Background: The presence of FLT3-internal tandem duplication (ITD) in patients (pts) with acute myeloid leukemia (AML) is…
Expand
Highly Cited
2013
Highly Cited
2013
Activity of ponatinib against clinically-relevant AC220-resistant kinase domain mutants of FLT3-ITD.
Catherine C. Smith
,
E. A. Lasater
,
+5 authors
N. Shah
Blood
2013
Corpus ID: 206913664
Secondary point mutations in the Fms-like tyrosine kinase 3 (FLT3) tyrosine kinase domain (KD) are common causes of acquired…
Expand
2013
2013
AC220 (Quizartinib) Can Be Safely Combined With Conventional Chemotherapy In Older Patients With Newly Diagnosed Acute Myeloid Leukaemia: Experience From The AML18 Pilot Trial
A. Burnett
,
D. Bowen
,
+8 authors
R. Hills
2013
Corpus ID: 70646406
Introduction AC220 (Quizartinib) is a novel FLT3 inhibitor that has shown a high level of activity as monotherapy in patients…
Expand
2013
2013
The E3 ubiquitin ligase TRAF2 can contribute to TNF-α resistance in FLT3-ITD-positive AML cells.
U. Schnetzke
,
M. Fischer
,
+4 authors
S. Scholl
Leukemia research : a Forum for Studies on…
2013
Corpus ID: 35631609
2013
2013
Results Of a Phase 2 Randomized, Open-Label, Study Of Lower Doses Of Quizartinib (AC220; ASP2689) In Subjects With FLT3-ITD Positive Relapsed Or Refractory Acute Myeloid Leukemia (AML)
M. Tallman
,
G. Schiller
,
+6 authors
M. Levis
2013
Corpus ID: 68645424
FMS-like tyrosine kinase 3 internal tandem duplications (FLT3-ITD) in acute myeloid leukemia (AML) are associated with early…
Expand
Review
2012
Review
2012
Molecular targeted therapy in acute myeloid leukemia
N. Daver
,
J. Cortes
Hematology
2012
Corpus ID: 20632081
The treatment of acute myeloid leukemia has not changed significantly over the last 40 years. Recent progress in understanding…
Expand
Highly Cited
2009
Highly Cited
2009
AC220, a Potent, Selective, Second Generation FLT3 Receptor Tyrosine Kinase (RTK) Inhibitor, in a First-in-Human (FIH) Phase 1 AML Study.
J. Cortes
,
J. Foran
,
+14 authors
M. Trikha
2009
Corpus ID: 79469058
Abstract 636 Activating mutations in the FLT3 RTK are present in ∼30% of AML patients (pts), who have a significantly worse…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE