A Phase II Study of Azacitidine, Venetoclax, and Trametinib in Relapsed or Refractory Acute Myeloid Leukemia Harboring RAS Pathway-Activating Mutations
Author(s) -
Sai Prasad Desikan,
Farhad Ravandi,
Naveen Pemmaraju,
Marina Konopleva,
Sanam Loghavi,
Elias Jabbour,
Naval Daver,
Nitin Jain,
Kelly S. Chien,
Abhishek Maiti,
Guillermo MontalbanBravo,
Tapan M. Kadia,
Walid Macaron,
Ricardo Delumpa,
Monica Kwari,
Gautam Borthakur,
Nicholas J. Short
Publication year - 2022
Publication title -
acta haematologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 56
eISSN - 1421-9662
pISSN - 0001-5792
DOI - 10.1159/000525566
Subject(s) - venetoclax , azacitidine , trametinib , medicine , myeloid leukemia , oncology , adverse effect , leukemia , biology , mapk/erk pathway , biochemistry , gene expression , chronic lymphocytic leukemia , kinase , dna methylation , gene , microbiology and biotechnology
RAS pathway mutations are common mechanisms of resistance to acute myeloid leukemia (AML) therapies. Trametinib, an oral MEK inhibitor, has been shown to have single-agent activity in relapsed/refractory AML and preclinical synergy with venetoclax.
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