Article
Impact of splicing mutations in acute myeloid leukemia treated with hypomethylating agents combined with venetoclax.
Blood advances - 27 Apr 2021
Lachowiez Curtis A, Loghavi Sanam, Furudate Ken, Montalban-Bravo Guillermo, Maiti Abhishek, Kadia Tapan, Daver Naval, Borthakur Gautam, Pemmaraju Naveen, Sasaki Koji, Alvarado Yesid, Yilmaz Musa, Short Nicholas J, Chien Kelly, Ohanian Maro, Pierce Sherry, Patel Keyur P, Jabbour Elias, Ravandi Farhad, Kantarjian Hagop M, Garcia-Manero Guillermo, Takahashi Koichi, Konopleva Marina Y, DiNardo Courtney D
Abstract excerpt
Spliceosome mutations (SRSF2, SF3B1, U2AF1, ZRSR2), are encountered in ∼50% of secondary acute myeloid leukemia cases (sAML) and define a molecular subgroup with outcomes similar to sAML in de novo AML patients treated with intensive chemotherapy. Outcomes in patients with spliceosome mutations treated with hypomethylating agents in combination with venetoclax (HMA+VEN) remains unknown. The primary objective was...
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