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

Metzeler, Klaus H., Maharry, Kati, Radmacher, Michael D., Mrózek, Krzysztof, Margeson, Dean, Becker, Heiko, Curfman, John, Holland, Kelsi B., Schwind, Sebastian, Whitman, Susan P., Wu, Yue-Zhong, Blum, William, Powell, Bayard L., Carter, Thomas H., Wetzler, Meir, Moore, Joseph O., Kolitz, Jonathan E., Baer, Maria R., Carroll, Andrew J., Larson, Richard A., Caligiuri, Michael A., Marcucci, Guido, Bloomfield, Clara D.·2011·Journal of Clinical Oncology

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.

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Metadata

Authors
Metzeler, K. H., Maharry, K., Radmacher, M. D., Mrózek, K., Margeson, D., Becker, H., Curfman, J., Holland, K. B., Schwind, S., Whitman, S. P., Wu, Y.-Z., Blum, W., Powell, B. L., Carter, T. H., Wetzler, M., Moore, J. O., Kolitz, J. E., Baer, M. R., Carroll, A. J., Larson, R. A., Caligiuri, M. A., Marcucci, G., & Bloomfield, C. D.
Affiliations
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...
Venue
Journal of Clinical Oncology
Published
2011-04-01
Volume
29
Issue
10
Pages
1373-1381
ISSN
  • 0732-183X
  • 1527-7755
Cited by
280
References
2
Language
en

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CoChat. (2026). Citation check: TET2 Mutations Improve the New European LeukemiaNet Risk Classification of Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study. https://app.cochat.ai/papers/10.1200/jco.2010.32.7742
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Metzeler, K. H., Maharry, K., Radmacher, M. D., Mrózek, K., Margeson, D., Becker, H., Curfman, J., Holland, K. B., Schwind, S., Whitman, S. P., Wu, Y.-Z., Blum, W., Powell, B. L., Carter, T. H., Wetzler, M., Moore, J. O., Kolitz, J. E., Baer, M. R., Carroll, A. J., . . . Bloomfield, C. D. (2011). TET2 Mutations Improve the New European LeukemiaNet Risk Classification of Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2010.32.7742