TET2 Mutations Improve the New European LeukemiaNet Risk Classification of Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study

Author:

Metzeler Klaus H.1,Maharry Kati1,Radmacher Michael D.1,Mrózek Krzysztof1,Margeson Dean1,Becker Heiko1,Curfman John1,Holland Kelsi B.1,Schwind Sebastian1,Whitman Susan P.1,Wu Yue-Zhong1,Blum William1,Powell Bayard L.1,Carter Thomas H.1,Wetzler Meir1,Moore Joseph O.1,Kolitz Jonathan E.1,Baer Maria R.1,Carroll Andrew J.1,Larson Richard A.1,Caligiuri Michael A.1,Marcucci Guido1,Bloomfield Clara D.1

Affiliation:

1. From the Ohio State University Comprehensive Cancer Center, Columbus, OH; Cancer and Leukemia Group B Statistical Center, Duke University Medical Center, Durham; Comprehensive Cancer Center of Wake Forest University, Winston-Salem, NC; University of Iowa, Iowa City, IA; Roswell Park Cancer Institute, Buffalo; North Shore University Hospital, Manhasset, NY; Greenebaum Cancer Center, University of Maryland, Baltimore, MD; University of Alabama at Birmingham, Birmingham, AL; and The University of Chicago...

Abstract

Purpose To determine the frequency of TET2 mutations, their associations with clinical and molecular characteristics and outcome, and the associated gene- and microRNA-expression signatures in patients with primary cytogenetically normal acute myeloid leukemia (CN-AML). Patients and Methods Four-hundred twenty-seven patients with CN-AML were analyzed for TET2 mutations by polymerase chain reaction and direct sequencing and for established prognostic gene mutations. Gene- and microRNA-expression profiles were derived using microarrays. Results TET2 mutations, found in 23% of patients, were associated with older age (P < .001) and higher pretreatment WBC (P = .04) compared with wild-type TET2 (TET2-wt). In the European LeukemiaNet (ELN) favorable-risk group (patients with CN-AML who have mutated CEBPA and/or mutated NPM1 without FLT3 internal tandem duplication [FLT3-ITD]), TET2-mutated patients had shorter event-free survival (EFS; P < .001) because of a lower complete remission (CR) rate (P = .007), and shorter disease-free survival (DFS; P = .003), and also had shorter overall survival (P = .001) compared with TET2-wt patients. TET2 mutations were not associated with outcomes in the ELN intermediate-I–risk group (CN-AML with wild-type CEBPA and wild-type NPM1 and/or FLT3-ITD). In multivariable models, TET2 mutations were associated with shorter EFS (P = .004), lower CR rate (P = .03), and shorter DFS (P = .05) only among favorable-risk CN-AML patients. We identified a TET2 mutation-associated gene-expression signature in favorable-risk but not in intermediate-I–risk patients and found distinct mutation-associated microRNA signatures in both ELN groups. Conclusion TET2 mutations improve the ELN molecular-risk classification in primary CN-AML because of their adverse prognostic impact in an otherwise favorable-risk patient subset. Our data suggest that these patients may be candidates for alternative therapies.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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