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Impact of the variant allele frequency of ASXL1, DNMT3A, JAK2, TET2, TP53, and NPM1 on the outcomes of patients with newly diagnosed acute myeloid leukemia

  • Koji Sasaki
    ,
  • Rashmi Kanagal-Shamanna
    ,
  • Guillermo Montalban-Bravo
    ,
  • Rita Assi
    ,
  • Elias Jabbour
    ,
  • Farhad Ravandi
*Corresponding author for this work
  • University of Texas MD Anderson Cancer Center
    ,
  • Tokyo Medical and Dental University
    ,
  • Lebanese American University
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Background: The impact of the allelic burden of ASXL1, DNMT3A, JAK2, TET2, and TP53 mutations on survival remains unclear in patients with newly diagnosed acute myeloid leukemia (AML). Methods: The authors assessed bone marrow aspirates from 421 patients with newly diagnosed AML using next-generation sequencing for ASXL1, DNMT3A, JAK2, TET2, and TP53 mutations, defined as the presence of mutations in ASXL1, DNMT3A, JAK2, TET2, or TP53 with a minimum variant allele frequency (VAF) of 5%. Results: A total of 71 patients (17%) had ASXL1 mutations, 104 patients (25%) had DNMT3A mutations, 16 patients (4%) had JAK2 mutations, 82 patients (20%) had TET2 mutations, and 86 patients (20%) had TP53 mutations. Among patients with each mutation, the median VAF of ASXL1 was 34.31% (range, 1.17%-58.62%), the median VAF of DNMT3A was 41.76% (range, 1.02%-91.66%), the median VAF of JAK2 was 46.70% (range, 10.4%-71.7%), the median VAF of TET2 was 42.78% (range, 2.26%-95.32%), and the median VAF of TP53 was 45.47% (range, 1.15%-93.74%). The composite complete response rate was 60%, and was 77% in patients with AML with and without ASXL1, DNMT3A, JAK2, TET2, or TP53 mutations, respectively (P =.006); the median overall survival was 11 months and 27 months, respectively (P <.001). Multivariate analysis identified age; an antecedent history of dysplasia; white blood cell count; adverse cytogenetic risk; previous treatment with an FLT3 inhibitor; and the VAF of ASXL1, DNMT3A, JAK2, TET2, TP53, and NPM1 mutations by next-generation sequencing as prognostic factors for overall survival. Conclusions: The VAF of ASXL1, DNMT3A, JAK2, TET2, TP53, and NPM1 mutations is associated with worse prognosis in patients with newly diagnosed AML.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 765-774 (10 pages)

Journal (Volume, Issue Number)

Cancer (Volume 126, Issue 4)

Publication milestones

  • Published - 02/15/2020

Publication status

Published - 02/15/2020

ISSN

0008-543X

Publication IDs

  • Scopus: 85075500054
  • PubMed: 31742675
  • ORCID: /0000-0002-8636-1071/work/68887895

Publication metrics

Metrics

SciVal
citations
16
SciVal
FWCI
5.86
SciVal
Author count
15
SciVal
Paper percentile
98
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.07
Fractional count
14
Fractional count
0.93
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
89
Citation count
99

Funding Details

Supported in part by The University of Texas MD Anderson Cancer Center Support Grant CA016672, The University of Texas MD Anderson MDS/AML Moon Shot, and Leukemia Texas. Supported in part by The University of Texas MD Anderson Cancer Center Support Grant CA016672, The University of Texas MD Anderson MDS/AML Moon Shot, and Leukemia Texas.
FundersFunding numbers
Leukemia Texas
-
NCI
P30CA016672
MD Anderson Cancer Center
CA016672