Evidence map›Paper›PMID 27529817›Full record

ArticleCancer2017

A novel prognostic model for osteosarcoma using circulating CXCL10 and FLT3LG.

Ricardo J Flores, Aaron J Kelly, Yiting Li, Manjula Nakka, Donald A Barkauskas, Mark Krailo, Lisa L Wang, Laszlo Perlaky, Ching C Lau, M John Hicks and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Interferon-γ-Inducible Chemokines as Prognostic Markers for Lung Cancer.International journal of environmental research and public health · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. CXCL-10: a new candidate for melanoma therapy?Cellular oncology (Dordrecht, Netherlands) · 2020
    Review
  18. Article
  19. Article
  20. 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

11 authors at 5 institutions in 1 country.

Ricardo J FloresTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Aaron J KellyTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Yiting LiTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Manjula NakkaTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Donald A BarkauskasDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.
Mark KrailoDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.
Lisa L WangTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Laszlo PerlakyTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Ching C LauTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
M John HicksDan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas.
Tsz-Kwong ManTexas Children's Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
Baylor College of Medicine · USTexas Children's Hospital · USChildren's Cancer Center · USChildren's Oncology Group · 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
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ANDERSON, JAMES R · 2003 to 2013
$67.5M
PEDIATRIC ONCOLOGY CLINICAL RESEARCH TRAINING PROGRAMK12CA090433 · NCI · BAYLOR COLLEGE OF MEDICINE · PI CARL E ALLEN, Donald W. Parsons · 2002 to 2026
$18.5M
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
Initiative for Maximizing Student Development (IMSD) ProgramR25GM056929 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI PEREIRA, FRED A · 1998 to 2023
$12.4M
NCI NIH HHS K12 CA090433NCI NIH HHS P30 CA125123NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA114766NIGMS NIH HHS R25 GM056929
6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is the most common malignant pediatric bone tumor. The identification of novel biomarkers for early prognostication will facilitate risk-based stratification and therapy. This study investigated the significance of circulating cytokines/chemokines for predicting the prognosis at the initial diagnosis.

methodsLuminex assays were used to measure cytokine/chemokine concentrations in blood samples from a discovery cohort of OS patients from Texas Children's Hospital (n = 37) and an independent validation cohort obtained from the Children's Oncology Group (n = 233). After the validation of the biomarkers, a multivariate model was constructed to stratify the patients into risk groups.

resultsThe circulating concentrations of C-X-C motif chemokine ligand 10 (CXCL10), Fms-related tyrosine kinase 3 ligand (FLT3LG), interferon γ (IFNG), and C-C motif chemokine ligand 4 (CCL4) were significantly associated with overall survival in both cohorts. Among these candidates, CXCL10 and FLT3LG were independent of the existing prognostic factor, metastasis at diagnosis, and CCL4 further discriminated cancer cases from controls. CXCL10, FLT3LG, and the metastatic status at diagnosis were combined to develop a multivariate model that significantly stratified the patients into 4 distinct risk groups (P = 1.6 × 10

conclusionsHigh circulating levels of CXCL10 and FLT3LG predicted worse survival for patients with OS. Because both CXCL10 and FL3LG axes are potentially targetable, further study may lead to novel risk-based stratification and therapy for OS. Cancer 2017;144-154. © 2016 American Cancer Society.

Indexed as

AdolescentAdultBiomarkers, TumorBone NeoplasmsChemokine CXCL10ChildChild, PreschoolCytokinesDisease-Free SurvivalFemaleHumansMaleMembrane ProteinsOsteosarcomaPrognosisRiskBiomarkers, TumorChemokine CXCL10CXCL10 protein, humanCytokinesflt3 ligand proteinMembrane Proteinscirculating biomarkersCXCL10FLT3LGLuminexmetastasisosteosarcomapediatric cancer and prognosis

Identifiers

PMID27529817
PMCPMC5161556
OpenAlexW2519957847

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.