Literature DB >> 29741984

MYC protein expression is an important prognostic factor in acute myeloid leukemia.

Maro Ohanian1, Uri Rozovski2, Rashmi Kanagal-Shamanna3, Lynne V Abruzzo4, Sanam Loghavi3, Tapan Kadia1, Andrew Futreal5, Kapil Bhalla1, Zhuang Zuo3, Yang O Huh3, Sean M Post1, Peter Ruvolo1, Guillermo Garcia-Manero1, Michael Andreeff1, Steven Kornblau1, Gautam Borthakur1, Peter Hu6, L Jeffrey Medeiros3, Koichi Takahashi1, Marisa J Hornbaker1, Jianhua Zhang5, Graciela M Nogueras-González7, Xuelin Huang7, Srdan Verstovsek1, Zeev Estrov1, Sherry Pierce1, Farhad Ravandi1, Hagop M Kantarjian1, Carlos E Bueso-Ramos3, Jorge E Cortes1.   

Abstract

As new drugs targeting MYC show clinical activity in acute myeloid leukemia (AML), understanding MYC expression in AML is of critical importance. We assessed MYC protein expression by immunohistochemistry in bone marrow of patients with untreated AML (n = 265). Overall, 90% of patients demonstrated MYC overexpression and MYC immunopositivity ≤6% was associated with superior complete remission (CR) duration of 23 months versus 12 months for MYC immunopositivity >6% (p = .028). Among 241 patients at higher risk for relapse, including those ≥55 years of age and patients with intermediate- and high-risk AML, MYC immunopositivity ≤6% conferred significantly superior median overall survival (OS) (24 versus 13 months; p = .042), event-free survival (EFS) (14 versus 6 months; p = .048), and relapse-free survival (RFS) (25 versus 12 months; p = .024). The prognostic impact of MYC-immunopositivity was retained on multivariate analysis of OS, EFS, and RFS. We conclude that MYC immunopositivity is an important prognostic factor in patients with untreated AML, particularly those at higher risk for relapse.

Entities:  

Keywords:  Acute myeloid leukemia (AML); MYC; immunohistochemistry (IHC)

Mesh:

Substances:

Year:  2018        PMID: 29741984      PMCID: PMC6226369          DOI: 10.1080/10428194.2018.1464158

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


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