Evidence map›Paper›PMID 22089931›Full record

ArticleJournal of cancer research and clinical oncology2012

PAX3/7-FOXO1 fusion status in older rhabdomyosarcoma patient population by fluorescent in situ hybridization.

Sarah N Dumont, Alexander J Lazar, Julia A Bridge, Robert S Benjamin, Jonathan C Trent

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. The Role of the PAX Genes in Renal Cell Carcinoma.International journal of molecular sciences · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Distinct methylation profiles characterize fusion-positive and fusion-negative rhabdomyosarcoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2015
    Article
  11. Review
  12. Article
  13. The inconvenience of convenience cohorts: rhabdomyosarcoma and the PAX-FOXO1 biomarker.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2012
    Review
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

5 authors at 3 institutions in 1 country.

Sarah N DumontDepartment of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77054, USA. sarahndumont@yahoo.fr
Alexander J Lazar
Julia A Bridge
Robert S Benjamin
Jonathan C Trent
The University of Texas MD Anderson Cancer Center · USNebraska Medical Center · USUniversity of Miami · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Mechanism/activity/resistance/Gleevec/GI stromal tumors (K23M)K23CA109060 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TRENT, JONATHAN C · 2004 to 2008
$680k
NCI NIH HHS CA016672NCI NIH HHS K23 CA109060NCI NIH HHS K23CA109060-05NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposeIn pediatric alveolar rhabdomyosarcoma, the PAX3-FOXO1 and PAX7-FOXO1 gene fusions are prognostic indicators, while little is known concerning this disease in older patients. To determine whether PAX3/7-FOXO1 fusion gene status correlates with outcome in adolescent, young adult, and adult rhabdomyosarcoma patients, the histological, immunohistochemical, and clinical characteristics of 105 patients followed at The University of Texas MD Anderson Cancer Center from 1957 to 2001 were evaluated.

methodsThe samples were assembled into a tissue microarray, and fusion gene status was determined by fluorescence in situ hybridization using PAX3, PAX7, and FOXO1 loci-specific probes. The disease characteristics and specific gene fusion were correlated with patient outcomes using the log-rank test.

resultsFifty-two percent of the samples exhibited a PAX3-FOXO1 fusion, 15% the PAX7-FOXO1 fusion, and 33% were negative for a rearrangement of these loci. The presence of PAX3/7-FOXO1 translocation was significantly associated with a higher frequency of metastatic disease. Although a statistically significant correlation between the PAX3/7-FOXO1 fusion gene status and overall survival was not identified, there was a trend toward better outcomes for patients with fusion-negative RMS.

conclusionsTherefore, identification of a FOXO1 fusion appears to be an interesting tool for predicting outcomes in older rhabdomyosarcoma patients and is worth further investigations in this rare subgroup of RMS population.

Indexed as

Gene FusionAdolescentAdultAgedAged, 80 and overAge FactorsChildChild, PreschoolFemaleForkhead Box Protein O1Forkhead Transcription FactorsHumansInfantIn Situ Hybridization, FluorescenceMaleMiddle AgedForkhead Box Protein O1Forkhead Transcription FactorsFOXO1 protein, humanPaired Box Transcription FactorsPAX3 protein, humanPAX3 Transcription FactorPAX7 protein, humanPAX7 Transcription Factor

Identifiers

PMID22089931
PMCPMC3932368
OpenAlexW2095445212

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Registered trials

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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.