Evidence map›Paper›PMID 31346466›Full record

ArticleBiomarker research2019

A preliminary analysis of interleukin-1 ligands as potential predictive biomarkers of response to cetuximab.

Madelyn Espinosa-Cotton, Elana J Fertig, Laura P Stabile, Autumn Gaither-Davis, Julie E Bauman, Sandra Schmitz, Katherine N Gibson-Corley, Yinwen Cheng, Isaac J Jensen, Vladimir P Badovinac and 2 more

Abstract read
In one paragraph

Article in Biomarker research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
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  6. Review
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  8. Article
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

12 authors.

Madelyn Espinosa-Cotton1Free Radical and Radiation Biology Program, Department of Radiation Oncology, University of Iowa, Iowa City, IA USA.
Elana J Fertig4Division of Biostatistics and Bioinformatics, Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD USA.
Laura P Stabile5Department of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA USA.
Autumn Gaither-Davis5Department of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, PA USA.
Julie E Bauman6Division of Hematology and Oncology, University of Arizona Cancer Center, Tucson, AZ USA.
Sandra Schmitz7Université catholique de Louvain, Louvain-la-Neuve, Belgium.
Katherine N Gibson-Corley2Department of Pathology, 1161 Medical Laboratories, University of Iowa, Iowa City, IA 52242 USA.
Yinwen Cheng2Department of Pathology, 1161 Medical Laboratories, University of Iowa, Iowa City, IA 52242 USA.
Isaac J Jensen2Department of Pathology, 1161 Medical Laboratories, University of Iowa, Iowa City, IA 52242 USA.
Vladimir P Badovinac2Department of Pathology, 1161 Medical Laboratories, University of Iowa, Iowa City, IA 52242 USA.
Douglas Laux3Holden Comprehensive Cancer Center, University of Iowa Hospitals and Clinics, Iowa City, IA USA.
Andrean L Simons1Free Radical and Radiation Biology Program, Department of Radiation Oncology, University of Iowa, Iowa City, IA USA.

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI WILLIAM George NELSON · 1985 to 2026
$208.6M
Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
TUMOR SUPPRESOR GENE PROMOTER HYPERMETHYLATION FOR DETECTION OF HEAD AND NECKP50DE019032 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI SIDRANSKY, DAVID · 2007 to 2016
$27.1M
TRAINING IN MECHANISMS OF PARASITISMT32AI007511 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WEBER, MARY · 1996 to 2025
$8.1M
Role of inflammation in resistance to EGFR inhibitors in head and neck cancerR01DE024550 · NIDCR · UNIVERSITY OF IOWA · PI BURNETT, ANDREAN LLEWELA · 2014 to 2018
$2.0M
Dynamical Models of Cetuximab Resistance in HNSCC Based on Serial Genomics DataR01CA177669 · NCI · JOHNS HOPKINS UNIVERSITY · PI FERTIG, ELANA · 2014 to 2019
$1.8M
Targeting inflammation and immune response in HNSCC therapyF99CA223062 · NCI · UNIVERSITY OF IOWA · PI ESPINOSA-COTTON, MADELYN · 2017 to 2018
$61k
NCI NIH HHS F99 CA223062NCI NIH HHS P30 CA006973NCI NIH HHS R01 CA177669NIAID NIH HHS T32 AI007511NIDCR NIH HHS P50 DE019032NIDCR NIH HHS R01 DE024550
6 · The paper itself

Abstract

backgroundThe epidermal growth factor receptor (EGFR) monoclonal IgG

methodsBaseline gene, serum and tumor expression of interleukin-1 (IL-1) ligands were analyzed from The Cancer Genome Atlas (TCGA) database or clinical trials of cetuximab-based therapies and interrogated for associations with clinical outcome data.

resultsHigh tumor gene expression of IL-1β was associated with a more favorable overall survival in cetuximab-treated HNSCC patients but not in non-cetuximab-treated patients. In HNSCC patients treated with cetuximab-based chemotherapy, higher gene and circulating levels of IL-1α and IL-1β were correlated with a more favorable progression free survival compared to patients with low or undetectable levels of IL-1 ligands.

conclusionsThese findings suggest that IL-1 ligands may function as predictive biomarkers for tumor response to cetuximab-based chemotherapy in HNSCC patients and warrants further investigation and validation in larger clinical studies.

Indexed as

BiomarkerCetuximabHead and neck squamous cell carcinoma (HNSCC)Interleukin-1 (IL-1)

Identifiers

PMID31346466
PMCPMC6636109

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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.