Overview

NCI Definition: A rare mixed phenotype acute leukemia in which the blasts express T-lymphoid and myeloid lineage markers but are negative for MLL translocation and t(9;22)(q34;q11.2) translocation. The prognosis is usually unfavorable. [1]

Mixed phenotype acute leukemia, T/myeloid, NOSs most frequently harbor alterations in DNMT3A, RUNX1, JAK3, IDH2, and BCOR [2].

Most Commonly Altered Genes in Mixed Phenotype Acute Leukemia, T/Myeloid, NOS

RUNX1 Mutation, JAK3 Mutation, IDH2 R140Q, IDH2 Mutation, and IDH2 Exon 4 Mutation are the most common alterations in mixed phenotype acute leukemia, T/myeloid, NOS [2].

Top Alterations in Mixed Phenotype Acute Leukemia, T/Myeloid, NOS

Significant Genes in Mixed Phenotype Acute Leukemia, T/Myeloid, NOS

ABL1 +

ABL2 +

BCR +

CEP72 +

CRLF2 +

CSF1R +

EPOR +

FLT3 +

IL7R +

JAK1 +

JAK2 +

JAK3 +

PDGFRB +

SH2B3 +

Disease Details

Synonyms
Mixed Phenotype Acute Leukemia, T/Myeloid, Not Otherwise Specified
Parent(s)
Mixed Phenotype Acute Leukemia
OncoTree Name
Mixed Phenotype Acute Leukemia, T/Myeloid, NOS
OncoTree Code
MPALTNOS

References

1. National Cancer Institute. NCI Thesaurus Version 18.11d. https://ncit.nci.nih.gov/ncitbrowser/ [2018-08-28]. [2018-09-21].

2. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.

3. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.