Evidence map›Paper›PMID 25687833›Full record

ArticleLeukemia research2015

Increased likelihood of post-polycythemia vera myelofibrosis in Ph-negative MPN patients with chromosome 12 abnormalities.

Christopher B Benton, Maria Tanaka, Catherine Wilson, Sherry Pierce, Lingsha Zhou, Jorge Cortes, Hagop Kantarjian, Srdan Verstovsek

Open access · greenAbstract read
In one paragraph

Article in Leukemia research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Chromosome 12 Rearrangement in an Adolescent with Primary Myelofibrosis.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2019
    Article
  6. Article
  7. Article
  8. Review
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Christopher B BentonDivision of Cancer Medicine, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Maria TanakaDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Catherine WilsonDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Sherry PierceDepartment of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Lingsha ZhouDepartment of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Jorge CortesDepartment of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Hagop KantarjianDepartment of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Srdan VerstovsekDepartment of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA. Electronic address: sverstov@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Chromosome 12 (Chr12) abnormalities have been described for individual patients with Philadelphia chromosome-negative myeloproliferative neoplasms (Ph-neg MPN), however the frequency, characteristics, and outcomes of such patients as a whole have not been investigated. We reviewed a database of 1787 consecutive Ph-neg MPN patients seen at our institution and determined that 2% of Ph-neg MPN patients harbored an alteration involving Chr12 by cytogenetic evaluation. Retrospective chart review revealed that patients with Chr12 abnormalities had a higher likelihood of having myelofibrosis (MF) compared to patients without a Chr12 abnormality, and were more likely to have post-polycythemia vera MF. The most common alterations in Chr12 in MF patients involved 12q13, 12q15, 12q24, and trisomy 12, and >40% of Chr12 Ph-neg MPN patients had cytogenetic evolution. Chr12 abnormalities did not significantly correlate with JAK2 status, progression to acute myeloid leukemia, or survival, however patients with 12q24 abnormalities trended toward poorer outcomes.

Indexed as

Chromosome AberrationsPhiladelphia ChromosomeAdultAgedAged, 80 and overChromosomes, Human, Pair 12FemaleFollow-Up StudiesHumansMaleMiddle AgedMyeloproliferative DisordersNeoplasm StagingPolycythemia VeraPrimary MyelofibrosisPrognosisChromosome aberrationsMyelofibrosisMyeloproliferative neoplasmsPolycythemia vera

Identifiers

PMID25687833
PMCPMC4847531
OpenAlexW2025652302

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.