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Diagnosing AML and determining prognosis are critical
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Acute myeloid leukemia (AML) is confirmed by bone marrow biopsy using morphologic, cytochemical, immunophenotypic, and cytogenetic/molecular analysis1
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AML evolves rapidly because of its polyclonal and heterogeneous features, contributing to the clinical challenges of this disease2
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As an indicator of prognosis, cytogenetic and molecular mutation testing are recommended by the National Comprehensive Cancer Network® (NCCN®) at diagnosis1
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Common molecular genetic mutations in AML (≥10%)3
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Molecular genetic testing may be an important factor that can be utilized to facilitate clinical decision-making1
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References: 1. Referenced with permission from the NCCN Clinical Practice Guidelines In Oncology (NCCN Guidelines®) for Acute Myeloid Leukemia V.2.2016. © National Comprehensive Cancer Network, Inc 2016. All rights reserved. Accessed June 29, 2016. To view the most recent and complete version of the guideline, go online to NCCN.org. NATIONAL COMPREHENSIVE CANCER NETWORK®, NCCN®, NCCN GUIDELINES®, and all other NCCN Content are trademarks owned by the National Comprehensive Cancer Network, Inc. 2. Ferrara F, Schiffer CA. Acute myeloid leukaemia in adults. Lancet. 2013;381(9865):484-495. 3. Patel JP, Gönen M, Figueroa ME, et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med. 2012;366(12):1079-1089.
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