Evidence map›Paper›PMID 29210060›Full record

ArticleInternational journal of cancer2018

Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients.

Roelof Koster, Orestis A Panagiotou, William A Wheeler, Eric Karlins, Julie M Gastier-Foster, Silvia Regina Caminada de Toledo, Antonio S Petrilli, Adrienne M Flanagan, Roberto Tirabosco, Irene L Andrulis and 21 more

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Etoposide activates CD8Journal for immunotherapy of cancer · 2025
    Article
  3. Article
  4. Article
  5. MFNG is an independent prognostic marker for osteosarcoma.European journal of medical research · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Two HLA Class II Gene Variants Are Independently Associated with Pediatric Osteosarcoma Risk.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2018
    Article
  17. Review
  18. IL-33 in Tumor Immunity: Nothing to Sneeze At.Critical reviews in immunology · 2018
    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

31 authors at 13 institutions in 7 countries.

Roelof KosterDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.ORCID 0000-0003-1424-8579
Orestis A PanagiotouDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
William A WheelerInformation Management Services (IMS), Inc. Rockville, MD.
Eric KarlinsDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Julie M Gastier-FosterThe Ohio State University Department of Pathology and Pediatrics, Nationwide Children's Hospital, Columbus, OH.
Silvia Regina Caminada de ToledoLaboratorio de Genética, Pediatric Oncology Institute, GRAACC/UNIFESP, São Paulo, Brazil.
Antonio S PetrilliLaboratorio de Genética, Pediatric Oncology Institute, GRAACC/UNIFESP, São Paulo, Brazil.
Adrienne M FlanaganUCL Cancer Institute, Huntley Street, London, United Kingdom.
Roberto TiraboscoRoyal National Orthopaedic Hospital NHS Trust, Stanmore, Middlesex, United Kingdom.
Irene L AndrulisLitwin Centre for Cancer Genetics, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.
Jay S WunderLitwin Centre for Cancer Genetics, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.
Nalan GokgozLitwin Centre for Cancer Genetics, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada.
Ana Patiño-GarciaDepartment of Pediatrics, University Clinic of Navarra, Universidad de Navarra, Pamplona, Spain.
Fernando LecandaDepartment of Pediatrics, University Clinic of Navarra, Universidad de Navarra, Pamplona, Spain.
Massimo SerraLaboratory of Experimental Oncology, Orthopaedic Rizzoli Institute, Bologna, Italy.
Claudia HattingerLaboratory of Experimental Oncology, Orthopaedic Rizzoli Institute, Bologna, Italy.
Piero PicciLaboratory of Experimental Oncology, Orthopaedic Rizzoli Institute, Bologna, Italy.
Katia ScotlandiLaboratory of Experimental Oncology, Orthopaedic Rizzoli Institute, Bologna, Italy.
David M ThomasThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Mandy L BallingerThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Richard GorlickDepartment of Pediatrics, University of Texas, MD Anderson Cancer Center, Houston, Texas, US.
Donald A BarkauskasKeck School of Medicine, University of Southern California, Los Angeles, CA.
Logan G SpectorDepartment of Pediatrics, University of Minnesota Minneapolis, MN.
Margaret TuckerDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
D Hicks BelyndaDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Meredith YeagerDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Robert N HooverDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Sholom WacholderDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Stephen J ChanockDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Sharon A SavageDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Lisa MirabelloDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
National Institutes of Health · USIstituto Ortopedico Rizzoli · ITLeidos (United States) · USMount Sinai Hospital · CAClinica Universidad de Navarra · ESGarvan Institute of Medical Research · AURoyal National Orthopaedic Hospital NHS Trust · GBSupport group for adolescents and children with cancer · BRInformation Management Services · USNationwide Children's Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity of Minnesota · USUniversity of Southern California · 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
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Genetic Modifiers of Cancer RiskZIACP010142 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI MIRABELLO, LISA · 2009 to 2025
$17.1M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
Intramural NIH HHS ZIA CP010142NCI NIH HHS P30 CA016058NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA114766
6 · The paper itself

Abstract

Survival rates for osteosarcoma, the most common primary bone cancer, have changed little over the past three decades and are particularly low for patients with metastatic disease. We conducted a multi-institutional genome-wide association study (GWAS) to identify germline genetic variants associated with overall survival in 632 patients with osteosarcoma, including 523 patients of European ancestry and 109 from Brazil. We conducted a time-to-event analysis and estimated hazard ratios (HR) and 95% confidence intervals (CI) using Cox proportional hazards models, with and without adjustment for metastatic disease. The results were combined across the European and Brazilian case sets using a random-effects meta-analysis. The strongest association after meta-analysis was for rs3765555 at 9p24.1, which was inversely associated with overall survival (HR = 1.76; 95% CI 1.41-2.18, p = 4.84 × 10

Indexed as

AdultAllelesBone NeoplasmsBrazilFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansInterleukin-33MaleMiddle AgedOsteosarcomaPolymorphism, Single NucleotideProportional Hazards ModelsSurvival RateIL33 protein, humanInterleukin-33genome-wide association studyosteosarcomaosteosarcoma-specific survivaloverall survival

Identifiers

PMID29210060
PMCPMC5814322
OpenAlexW2774577366

What OpenQuestion holds

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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.