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Midostaurin: an emerging treatment for acute myeloid leukemia patients
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scholarly article
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review article
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Europe PubMed Central
title
Midostaurin: an emerging treatment for acute myeloid leukemia patients
(English)
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main subject
leukemia
1 reference
based on heuristic
inferred from title
acute myeloid leukemia
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author
Hillard M. Lazarus
series ordinal
2
object named as
Hillard M Lazarus
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author name string
Molly Megan Gallogly
series ordinal
1
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language of work or name
English
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publication date
2016
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published in
Journal of Blood Medicine
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volume
7
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page(s)
73-83
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copyright license
Creative Commons Attribution-NonCommercial 3.0 Unported
start time
1 April 2016
1 reference
stated in
April 2022 Public Data File from Crossref
copyright status
copyrighted
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cites work
Absence of the wild-type allele predicts poor prognosis in adult de novo acute myeloid leukemia with normal cytogenetics and the internal tandem duplication of FLT3: a cancer and leukemia group B study.
1 reference
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Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
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Phase IIB trial of oral Midostaurin (PKC412), the FMS-like tyrosine kinase 3 receptor (FLT3) and multi-targeted kinase inhibitor, in patients with acute myeloid leukemia and high-risk myelodysplastic syndrome with either wild-type or mutated FLT3.
1 reference
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PubMed Central
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7 April 2017
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
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PubMed Central
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7 April 2017
Cancer statistics, 2015
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PubMed Central
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7 April 2017
Acute Myeloid Leukemia
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PubMed Central
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7 April 2017
Dose- and time-dependent pharmacokinetics of midostaurin in patients with diabetes mellitus
1 reference
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PubMed Central
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7 April 2017
FLT3 Tyrosine Kinase Inhibition as a Paradigm for Targeted Drug Development in Acute Myeloid Leukemia
1 reference
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PubMed Central
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28 September 2017
A phase I study of midostaurin and azacitidine in relapsed and elderly AML patients
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 September 2017
Phase I/II trial of the combination of midostaurin (PKC412) and 5-azacytidine for patients with acute myeloid leukemia and myelodysplastic syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 September 2017
Pre-leukemic evolution of hematopoietic stem cells: the importance of early mutations in leukemogenesis
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28 September 2017
FLT3 inhibitors in AML: are we there yet?
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28 September 2017
Investigation into CYP3A4-mediated drug-drug interactions on midostaurin in healthy volunteers
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PubMed Central
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28 September 2017
Crenolanib is active against models of drug-resistant FLT3-ITD-positive acute myeloid leukemia
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PubMed Central
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28 September 2017
Phase I study of quizartinib administered daily to patients with relapsed or refractory acute myeloid leukemia irrespective of FMS-like tyrosine kinase 3-internal tandem duplication status
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 September 2017
Preclinical and phase I results of decitabine in combination with midostaurin (PKC412) for newly diagnosed elderly or relapsed/refractory adult patients with acute myeloid leukemia
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PubMed Central
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28 September 2017
FLT3 inhibition: a moving and evolving target in acute myeloid leukaemia
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PubMed Central
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28 September 2017
Phase IB study of the FLT3 kinase inhibitor midostaurin with chemotherapy in younger newly diagnosed adult patients with acute myeloid leukemia
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PubMed Central
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28 September 2017
Mechanisms of resistance against PKC412 in resistant FLT3-ITD positive human acute myeloid leukemia cells
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PubMed Central
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28 September 2017
FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML.
1 reference
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PubMed Central
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28 September 2017
FLT3 inhibition as a targeted therapy for acute myeloid leukemia
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PubMed Central
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28 September 2017
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML)
1 reference
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PubMed Central
reference URL
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28 September 2017
Clinical resistance to the kinase inhibitor PKC412 in acute myeloid leukemia by mutation of Asn-676 in the FLT3 tyrosine kinase domain
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 September 2017
Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412.
1 reference
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PubMed Central
reference URL
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28 September 2017
Phase I and pharmacokinetic study of PKC412, an inhibitor of protein kinase C.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 September 2017
Inhibitors of protein kinases: CGP 41251, a protein kinase inhibitor with potential as an anticancer agent
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PubMed Central
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28 September 2017
Insertion of FLT3 internal tandem duplication in the tyrosine kinase domain-1 is associated with resistance to chemotherapy and inferior outcome.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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31 May 2018
A mechanism-based population pharmacokinetic model for characterizing time-dependent pharmacokinetics of midostaurin and its metabolites in human subjects
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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31 May 2018
Preliminary data on ASP2215: tolerability and efficacy in acute myeloid leukemia patients.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 November 2018
Sorafenib in Relapsed AML With FMS-Like Receptor Tyrosine Kinase-3 Internal Tandem Duplication Mutation.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 November 2018
FLT3 INHIBITORS: RECENT ADVANCES AND PROBLEMS FOR CLINICAL APPLICATION.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 November 2018
Sorafenib in combination with intensive chemotherapy in elderly patients with acute myeloid leukemia: results from a randomized, placebo-controlled trial.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
retrieved
28 November 2018
Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 November 2018
Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: a study of the AML Study Group Ulm.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4848023
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28 November 2018
Risk stratification of intermediate-risk acute myeloid leukemia: integrative analysis of a multitude of gene mutation and gene expression markers
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27186148
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
PKC412--a protein kinase inhibitor with a broad therapeutic potential
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27186148
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.2147/JBM.S100283
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2213744
OpenCitations bibliographic resource ID
2213744
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2213744
PMCID
4848023
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2213744
PubMed ID
27186148
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2213744
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