Evidence map›Paper›PMID 24831857›Full record

ArticleCancer causes & control : CCC2014

Maternal and birth characteristics and childhood rhabdomyosarcoma: a report from the Children's Oncology Group.

Philip J Lupo, Heather E Danysh, Stephen X Skapek, Douglas S Hawkins, Logan G Spector, Renke Zhou, M Fatih Okcu, Karin Papworth, Erik B Erhardt, Seymour Grufferman

Open access · greenAbstract read
In one paragraph

Article in Cancer causes & control : CCC, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Rhabdomyosarcoma.Nature reviews. Disease primers · 2019
    Review
  12. Article
  13. Article
  14. Rhabdomyosarcoma in adults: new perspectives on therapy.Current treatment options in oncology · 2015
    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

10 authors at 7 institutions in 2 countries.

Philip J LupoDepartment of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA, philip.lupo@bcm.edu.
Heather E Danysh
Stephen X Skapek
Douglas S Hawkins
Logan G Spector
Renke Zhou
M Fatih Okcu
Karin Papworth
Erik B Erhardt
Seymour Grufferman
Baylor College of Medicine · USChildren's Cancer Center · USUniversity of New Mexico · USChildren's Medical Center · USFred Hutch Cancer Center · USUmeå University · SEUniversity of Minnesota · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
CHILDRENS CANCER STUDY GROUP CHAIRMAN'S GRANTU10CA013539 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI REAMAN, GREGORY H · 1985 to 2002
$43.1M
PEDIATRIC ONCOLOGY GROUP-OPERATIONS OFFICEU10CA030969 · NCI · WASHINGTON UNIVERSITY · PI REAMAN, GREGORY H · 1985 to 2002
$24.8M
PEDIATRIC ONCOLOGY GROUP STATISTICAL OFFICEU10CA029139 · NCI · UNIVERSITY OF FLORIDA · PI DEVIDAS, MEENAKSHI · 1985 to 2002
$7.3M
INTERGROUP RHABDOMYOSARCOMA STUDYU10CA024507 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI REAMAN, GREGORY H · 1985 to 2002
$2.0M
THE EPIDEMIOLOGY OF CHILDHOOD RHABDOMYOSARCOMAR01CA021244 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GRUFFERMAN, SEYMOUR NONE · 1985 to 1988
–
NCI NIH HHS CA13539NCI NIH HHS CA21244NCI NIH HHS CA29139NCI NIH HHS CA30318NCI NIH HHS CA30969NCI NIH HHS U10 CA024507NCI NIH HHS U10 CA029139NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

purposePrevious assessments of childhood rhabdomyosarcoma have indicated maternal and birth characteristics may be associated with tumor development; however, much work remains to identify novel and confirm suspected risk factors. Our objective was to evaluate the associations between maternal and birth characteristics and childhood rhabdomyosarcoma.

methodsThis case-control study included 322 cases and 322 pair-matched controls. Cases were enrolled in a trial run by the Intergroup Rhabdomyosarcoma Study Group. Population-based controls were identified using random digit dialing and were individually matched to cases on race, sex, and age. Families of the case and control subjects participated in a telephone interview, which captured information on maternal characteristics (birth control use, number of prenatal visits, anemia, and abnormal bleeding during pregnancy) and birth characteristics [birth weight, preterm birth, and type of delivery (vaginal vs. cesarean)]. Conditional logistic regression models were used to calculate an odds ratio (OR) and 95% confidence interval (CI) for each exposure, adjusted for age, race, sex, household income, and parental education. As the two most common histologic types of rhabdomyosarcoma are embryonal (n = 215) and alveolar (n = 66), we evaluated effect heterogeneity of these exposures.

resultsThe only characteristic that was associated with childhood rhabdomyosarcoma, and statistically significant, was abnormal vaginal bleeding during pregnancy (OR 1.75, 95% CI 1.12-2.74). Birth control use (OR 1.45, 95% CI 0.96-2.18), anemia during pregnancy (OR 1.27, 95% CI 0.81-1.99), and preterm birth (OR 2.51, 95% CI 0.74-8.49) were positively associated with childhood rhabdomyosarcoma, but were not statistically significant. Low birth weight [adjusted odds ratios (aOR) 4.46, 95% CI 1.41-14.1] and high birth weight (aOR 2.41, 95% CI 1.09-5.35) were strongly associated with alveolar rhabdomyosarcoma. However, these factors did not display significant effect heterogeneity between histologic types (p > 0.15 for all characteristics).

conclusionsOverall, we found little evidence that these maternal and birth characteristics are strongly associated with childhood rhabdomyosarcoma.

Indexed as

Birth OrderBirth WeightCase-Control StudiesChildFemaleHumansMaleMaternal AgeOdds RatioPregnancyPregnancy ComplicationsRhabdomyosarcomaRisk Factors

Identifiers

PMID24831857
PMCPMC4091713
OpenAlexW1968901382

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.