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Dissecting AML treatment response to FLT3 inhibitors by single-cell sequencin (B12*)

Subject Area Hematology, Oncology
Term from 2020 to 2024
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 217328187
 
The constitutive activation of the FLT3 tyrosine kinase in AML via internal tandem duplications can be therapeutically targeted with the multi-kinase inhibitor midostaurin or the FLT3 specific drug gilteritinib, which are compared in a randomized phase III clinical trial (HOVON 156 / AMLSG 28-18). Differences between the two drugs as well as intra-tumor heterogeneity and its changes during this treatment are resolved in a comprehensive multi-omics single-cell sequencing analysis. It will reveal molecular features of leukemia cell subgroups, their response to treatment as well as changes of non-malignant cells in the microenvironment.
DFG Programme Collaborative Research Centres
Applicant Institution Universität Ulm
 
 

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