FLT3 Agonists and Secondary Hematopoietic Malignancies: A Potential Class Effect

Author:

Raeder Henry W.1ORCID,Drazer Michael W.23ORCID

Affiliation:

1. Department of Human Genetics, University of Chicago, Chicago, Illinois. 1

2. Hematology and Oncology, Department of Medicine, University of Chicago, Chicago, Illinois. 2

3. Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois. 3

Abstract

Summary Expansion of conventional dendritic cells via FMS-like tyrosine kinase 3 agonism has promising therapeutic potential in the treatment of advanced solid tumors. In this study, we discuss the results of a clinical trial using GS-3583, an FMS-like tyrosine kinase 3 agonist, that was stopped after a patient in the study developed acute myeloid leukemia. See related article by Tolcher et al., p. 2954

Publisher

American Association for Cancer Research (AACR)

Reference17 articles.

1. Phase I study of GS-3583, an FMS-like tyrosine kinase 3 agonist Fc fusion protein, in patients with advanced solid tumors;Tolcher;Clin Cancer Res,2024

2. Genomic correlates of response to immune checkpoint blockade;Keenan;Nat Med,2019

3. FLT3 targeting in the modern era: from clonal selection to combination therapies;Kennedy;Int J Hematol,2023

4. GS-3583, a novel FLT3 agonist Fc fusion protein, to expand conventional dendritic cells in healthy volunteers;Nishanthan;J Clin Oncol,2021

5. Age-related clonal hematopoiesis associated with adverse outcomes;Jaiswal;N Engl J Med,2014

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