New Drug for Chronic Myeloid Leukemia Might Stimulate the Market

The evolution of treatment options over the past 20 years has provided for a normal life expectancy for most patients with chronic myeloid leukemia. Currently approved tyrosine kinase inhibitors mainly differ in potency and side effect profile. Flumatinib goes for deep responses and good tolerabilit...

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Published inClinical cancer research Vol. 27; no. 1; pp. 3 - 4
Main Author Müller, Martin C.
Format Journal Article
LanguageEnglish
Published United States 01.01.2021
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Abstract The evolution of treatment options over the past 20 years has provided for a normal life expectancy for most patients with chronic myeloid leukemia. Currently approved tyrosine kinase inhibitors mainly differ in potency and side effect profile. Flumatinib goes for deep responses and good tolerability. See related article by Zhang et al., p. 70
AbstractList The evolution of treatment options over the past 20 years has provided for a normal life expectancy for most patients with chronic myeloid leukemia. Currently approved tyrosine kinase inhibitors mainly differ in potency and side effect profile. Flumatinib goes for deep responses and good tolerability. .
The evolution of treatment options over the past 20 years has provided for a normal life expectancy for most patients with chronic myeloid leukemia. Currently approved tyrosine kinase inhibitors mainly differ in potency and side effect profile. Flumatinib goes for deep responses and good tolerability.See related article by Zhang et al., p. 70.The evolution of treatment options over the past 20 years has provided for a normal life expectancy for most patients with chronic myeloid leukemia. Currently approved tyrosine kinase inhibitors mainly differ in potency and side effect profile. Flumatinib goes for deep responses and good tolerability.See related article by Zhang et al., p. 70.
The evolution of treatment options over the past 20 years has provided for a normal life expectancy for most patients with chronic myeloid leukemia. Currently approved tyrosine kinase inhibitors mainly differ in potency and side effect profile. Flumatinib goes for deep responses and good tolerability. See related article by Zhang et al., p. 70
Author Müller, Martin C.
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Cites_doi 10.1038/s41375-020-0776-2
10.1038/leu.2014.153
10.1038/leu.2010.169
10.1158/1078-0432.CCR-20-1600
10.1200/JCO.2009.26.3087
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Marin (2022061101492711500_bib2) 2010; 28
Hochhaus (2022061101492711500_bib4) 2020; 34
Hanfstein (2022061101492711500_bib3) 2014; 28
Luo (2022061101492711500_bib5) 2010; 24
32928796 - Clin Cancer Res. 2021 Jan 1;27(1):70-77
32928796 - Clin Cancer Res. 2020 Sep 14
References_xml – volume: 34
  start-page: 966
  year: 2020
  ident: 2022061101492711500_bib4
  article-title: European LeukemiaNet 2020 recommendations for treating chronic myeloid leukemia
  publication-title: Leukemia
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– volume: 28
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  year: 2014
  ident: 2022061101492711500_bib3
  article-title: Velocity of early BCR-ABL transcript elimination as an optimized predictor of outcome in chronic myeloid leukemia (CML) patients in chronic phase on treatment with imatinib
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– volume: 24
  start-page: 1807
  year: 2010
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  publication-title: Leukemia
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– volume: 27
  start-page: 70
  year: 2021
  ident: 2022061101492711500_bib1
  article-title: Flumatinib versus imatinib for newly diagnosed chronic phase chronic myeloid leukemia: a phase 3, randomized, open-label, multi-center FESTnd study
  publication-title: Clin Cancer Res
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– reference: 32928796 - Clin Cancer Res. 2021 Jan 1;27(1):70-77
– reference: 32928796 - Clin Cancer Res. 2020 Sep 14;:
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Title New Drug for Chronic Myeloid Leukemia Might Stimulate the Market
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