Evidence map›Paper›PMID 37335392›Full record

ArticleCancer causes & control : CCC2023

Birth characteristics and risk of Ewing sarcoma.

Joseph L Wiemels, Rong Wang, Qianxi Feng, Amy C Yee, Libby M Morimoto, Catherine Metayer, Xiaomei Ma

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Cancer causes & control : CCC, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Ewing sarcoma of the thumb presenting in a Hispanic patient: A case report.International journal of surgery case reports · 2024
    Article
  4. Primary cutaneous extraskeletal Ewing sarcoma of the plantar region: clinicopathological features and review of the literature.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

7 authors at 4 institutions in 1 country.

Joseph L WiemelsCenter for Genetic Epidemiology, Norris Comprehensive Cancer Center, University of Southern California, Keck School of Medicine, Norris Research Tower (NRT) 1506A, 1450 Biggy St, Los Angeles, CA, 90033, USA. wiemels@usc.edu.
Rong WangDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, USA.
Qianxi FengCenter for Genetic Epidemiology, Norris Comprehensive Cancer Center, University of Southern California, Keck School of Medicine, Norris Research Tower (NRT) 1506A, 1450 Biggy St, Los Angeles, CA, 90033, USA.
Amy C YeeCenter for Genetic Epidemiology, Norris Comprehensive Cancer Center, University of Southern California, Keck School of Medicine, Norris Research Tower (NRT) 1506A, 1450 Biggy St, Los Angeles, CA, 90033, USA.
Libby M MorimotoDepartment of Epidemiology, School of Public Health, University of California Berkeley, Berkeley, CA, USA.
Catherine MetayerDepartment of Epidemiology, School of Public Health, University of California Berkeley, Berkeley, CA, USA.
Xiaomei MaDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, USA.
University of California, Berkeley · USUSC Norris Comprehensive Cancer Center · USYale University · USUniversity of Southern California · US

Funding

Genome-Wide Association Study of Childhood Leukemia by Hispanic StatusR01CA155461 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MA, XIAOMEI, WIEMELS, JOSEPH LEO · 2011 to 2014
$4.1M
NIH HHS R01CA155461 R01CA194189
6 · The paper itself

Abstract

purposeThe incidence of Ewing sarcoma varies according to race and ethnicity, and genetic susceptibility is known to affect disease risk. Apart from these factors, the etiology of Ewing sarcoma is largely unknown.

methodsWe compared the birth characteristics of a population-based series of 556 Ewing sarcoma cases born in California in 1978-2015 and diagnosed in 1988-2015 with those of 27,800 controls selected from statewide birth records and frequency-matched to cases on the year of birth, using multivariable logistic regression models. We also assessed whether Ewing sarcoma clustered within families.

resultsCompared to non-Hispanic White subjects, Black (odds ratio [OR] = 0.07, 95% confidence interval [CI] 0.03-0.18), Asian (OR = 0.57, 95% CI 0.41-0.80), and Hispanic (OR = 0.73, 95% CI 0.62-0.88) individuals had a significantly lower risk of Ewing sarcoma. Race and ethnicity differences were more profound for metastatic Ewing sarcoma. Birthweight was also identified as a significant risk factor (OR = 1.09, 95% CI 1.00-1.18 for each 500 g increase in birthweight). A separate family-based cancer clustering analysis did not suggest any strong role for familial predisposition alleles.

conclusionsThis population-based study with minimal selection bias provides support for a role of accelerated fetal growth in the etiology of Ewing sarcoma in addition to more precise estimates of racial and ethnic variations in disease risk. This comparatively large analysis of birth characteristics and Ewing sarcoma in a multiethnic population should stimulate further investigations into genetic and environmental causes.

Indexed as

Sarcoma, EwingAsianBirth WeightBlack or African AmericanCaliforniaEthnicityFemaleHispanic or LatinoHumansRisk FactorsWhiteBirth characteristicsBirthweightChildhood cancerEpidemiologyEwing sarcoma

Identifiers

PMID37335392
PMCPMC10460323
OpenAlexW4381251404

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.