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Patients with polycythemia vera and essential thrombocythemia with prior malignancy do not have significantly worse outcome

  • Mohamad Cherry
    ,
  • Marylou Cardenas-Turanzas
    ,
  • Hannah Pham
    ,
  • Hagop Kantarjian
    ,
  • ,
  • Sherry Pierce
*Corresponding author for this work
  • University of Oklahoma
    ,
  • University of Texas MD Anderson Cancer Center
    ,
  • Texas Tech 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

The clinical relevance of prior malignancy (PM) in patients with essential thrombocythemia (ET) and polycythemia vera (PV) is largely unknown. We retrospectively evaluated 437 patients (ET, n= 263; PV, n= 174) treated at MD Anderson between 1960 and 2010. Forty-four patients had PM (ET, 10%; PV, 11%), with median time to diagnosis of 66 months. PM was not associated with abnormal cytogenetics, JAK2-mutation frequency, blood-cell counts or progression to acute leukemia or myelofibrosis. In multivariate analysis, only older age and high LDH levels were associated with worse OS. In conclusion, PM does not predict worse outcomes for patients with ET and PV.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1472-1476 (5 pages)

Journal (Volume, Issue Number)

Leukemia Research (Volume 37, Issue 11)

Publication milestones

  • Published - 11/2013

Publication status

Published - 11/2013

ISSN

0145-2126

Publication IDs

  • Scopus: 84886772830
  • PubMed: 23993426
  • ORCID: /0000-0002-8636-1071/work/68811160

Publication metrics

Metrics

Fractional count
1
Fractional count
0.13
Fractional count
7
Fractional count
0.88
Fractional count
1
Fractional count
1
SciVal
citations
3
SciVal
FWCI
0.08
SciVal
Author count
8
SciVal
Paper percentile
46
Scopus
citations

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5
Captures
19
Social media
19

Funding Details

This research is supported in part by the MD Anderson Cancer Center Support Grant CA016672 . We highly appreciate the help of Kate Newberry, PhD for scientific editing and Dr. Ali Alameri for his help with data collection.
FundersFunding numbers
MD Anderson Cancer Center Support
CA016672
NCI
P30CA016672