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Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets

For acute myeloid leukemia (AML), identification of activating mutations in the FMS-like tyrosine kinase-3 (FLT3) has led to the development of several FLT3-inhibitors. Here we present clinical and next generation sequencing data at the time of progression of a patient on a novel FLT3-inhibitor clin...

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Autores principales: Kasi, Pashtoon M., Litzow, Mark R., Patnaik, Mrinal M., Hashmi, Shahrukh K., Gangat, Naseema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726703/
https://www.ncbi.nlm.nih.gov/pubmed/26904404
http://dx.doi.org/10.1016/j.lrr.2016.01.002
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author Kasi, Pashtoon M.
Litzow, Mark R.
Patnaik, Mrinal M.
Hashmi, Shahrukh K.
Gangat, Naseema
author_facet Kasi, Pashtoon M.
Litzow, Mark R.
Patnaik, Mrinal M.
Hashmi, Shahrukh K.
Gangat, Naseema
author_sort Kasi, Pashtoon M.
collection PubMed
description For acute myeloid leukemia (AML), identification of activating mutations in the FMS-like tyrosine kinase-3 (FLT3) has led to the development of several FLT3-inhibitors. Here we present clinical and next generation sequencing data at the time of progression of a patient on a novel FLT3-inhibitor clinical trial (ASP2215) to show that employing therapeutic interventions with these novel targeted therapies can lead to consequences secondary to selective pressure and clonal evolution of cancer. We describe novel findings alongside data on treatment directed towards actionable aberrations acquired during the process. (Clinical Trial: NCT02014558; registered at: 〈https://clinicaltrials.gov/ct2/show/NCT02014558〉)
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spelling pubmed-47267032016-02-22 Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets Kasi, Pashtoon M. Litzow, Mark R. Patnaik, Mrinal M. Hashmi, Shahrukh K. Gangat, Naseema Leuk Res Rep Article For acute myeloid leukemia (AML), identification of activating mutations in the FMS-like tyrosine kinase-3 (FLT3) has led to the development of several FLT3-inhibitors. Here we present clinical and next generation sequencing data at the time of progression of a patient on a novel FLT3-inhibitor clinical trial (ASP2215) to show that employing therapeutic interventions with these novel targeted therapies can lead to consequences secondary to selective pressure and clonal evolution of cancer. We describe novel findings alongside data on treatment directed towards actionable aberrations acquired during the process. (Clinical Trial: NCT02014558; registered at: 〈https://clinicaltrials.gov/ct2/show/NCT02014558〉) Elsevier 2016-01-12 /pmc/articles/PMC4726703/ /pubmed/26904404 http://dx.doi.org/10.1016/j.lrr.2016.01.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kasi, Pashtoon M.
Litzow, Mark R.
Patnaik, Mrinal M.
Hashmi, Shahrukh K.
Gangat, Naseema
Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets
title Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets
title_full Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets
title_fullStr Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets
title_full_unstemmed Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets
title_short Clonal evolution of AML on novel FMS-like tyrosine kinase-3 (FLT3) inhibitor therapy with evolving actionable targets
title_sort clonal evolution of aml on novel fms-like tyrosine kinase-3 (flt3) inhibitor therapy with evolving actionable targets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726703/
https://www.ncbi.nlm.nih.gov/pubmed/26904404
http://dx.doi.org/10.1016/j.lrr.2016.01.002
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