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

Overview

abstract

  • UNLABELLED: 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〉).

publication date

  • January 12, 2016

Identity

PubMed Central ID

  • PMC4726703

Scopus Document Identifier

  • 84954149212

Digital Object Identifier (DOI)

  • 10.1016/j.lrr.2016.01.002

PubMed ID

  • 26904404

Additional Document Info

volume

  • 5