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Dynamic genetic and nongenetic RAS-pathway activation drives resistance to FLT3 and BCL2 inhibitor therapy.

Vanessa E Kennedy, Cheryl A C Peretz, Anushka Walia, Brenda Chyla, Yan Sun, Jason Hill, Elaine Tran, Andrew D Koh, Timothy Ferng, Samantha Pintar, Matthew F Jones, Bogdan Popescu, Isabelle Lomeli, Farid Chehab, Natalia Murad, August John, Ritu Roy, Adam Olshen, Christine A Berryhill, Christopher Davis, Steven P Angus, Jose M Rivera, Alicia Meshulam, Elliot Stieglitz, Sunil Joshi, Elie Traer, Monique Dail, Habib Hamidi, Jessica K Altman, Naval Daver, Mark Levis, James McCloskey, Alexander E Perl, Catherine C Smith

BloodSep 17, 2026PMID 42224378doi:10.1182/blood.2025032466 PMC13249044Clinical Trial, Phase IJournal ArticleMulticenter StudypubmedProvenance
Source
PubMed
Retrieved
Sep 30, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-PUBMED-20260930-000001
Published

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Bulk sequencing of relapsed tumors reveals mutations associated with resistance to cancer therapy but is insufficient to fully assess all causes of relapse. Because of inherent tumor heterogeneity, on-treatment tumor evolution may select genetically distinct clones or shifts in malignant…

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Registered trialsNCT03625505

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