Evidence map›Paper›PMID 28347290›Full record

ArticleBMC cancer2017

A possible association of baseline serum IL-17A concentrations with progression-free survival of metastatic colorectal cancer patients treated with a bevacizumab-based regimen.

Emilie Lereclus, Mira Tout, Alban Girault, Nadine Baroukh, Morgane Caulet, Christophe Borg, Olivier Bouché, David Ternant, Gilles Paintaud, Thierry Lecomte and 1 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00489697 (Medical and Economical Evaluation of Contrast-enhanced Ultrasound Imaging for the Early Estimate of Bevacizumab Effect on Colorectal Cancer Liver Metastases), which is not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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.

NCT00489697 nacompletednot on this map

Medical and Economical Evaluation of Contrast-enhanced Ultrasound Imaging for the Early Estimate of Bevacizumab Effect on Colorectal Cancer Liver Metastases

TypeinterventionalSponsorUniversity Hospital, ToursRan2007 to 2012Enrolled200ConditionsMetastatic Colorectal CancerArmsreal-time contrast-enhanced ultrasound imaging (CEUS)
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

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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 3 institutions in 1 country.

Emilie LereclusUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Mira ToutUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Alban GiraultUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Nadine BaroukhUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Morgane CauletUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Christophe BorgINSERM, UMR 1098, Department of Medical Oncology, University Hospital, Besançon, France.
Olivier BouchéDepartment of Hepato-Gastroenterology and Digestive Oncology, University Hospital Robert Debré, Reims, France.
David TernantUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Gilles PaintaudUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
Thierry LecomteUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France.
William RaoulUniversité François-Rabelais de Tours, CNRS, GICC UMR 7292, UFR de médecine, BP 3223, 10, boulevard Tonnellé, 37032, Tours Cedex 01, France. william.raoul@univ-tours.fr.
Université de Tours · FRHôpital Robert-Debré · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer is a major public health issue worldwide. Interleukin-17 (IL-17) and Th17 (T-helper cell type 17)-related molecules are involved in tumor development and in resistance to bevacizumab, an anti-vascular endothelial growth factor monoclonal antibody used in association with chemotherapy in metastatic colorectal cancer. Some studies have previously shown that IL-17A and IL-17F polymorphisms, respectively rs2275913 and rs763780, are associated with gastric or colorectal cancer risk. Here we aimed at studying the influence of IL-17A-related individual factors on overall survival and progression-free survival in patients with metastatic colorectal cancer treated with a bevacizumab-based chemotherapy.

methodsPre-treatment serum biomarkers were retrospectively evaluated in 122 metastatic colorectal cancer patients treated by bevacizumab in combination with chemotherapy at 2-weeks intervals in a prospective cohort study (NCT00489697). The polymorphisms of IL-17A and IL-17F were analyzed by polymerase chain reaction - restriction fragment length polymorphism. Serum concentrations of Th17-related cytokines were measured by MultiPlex. The impact of individual parameters on overall survival and progression-free survival was assessed using multivariate Cox models.

resultsHigh baseline IL-17A serum concentrations were significantly associated with shorter progression-free survival [p = 0.043]. Other baseline serum Th17-related cytokines and polymorphisms of IL-17 were not associated with overall survival or progression-free survival.

conclusionsIn this ancillary study, baseline serum IL-17A concentration is the only Th17/IL-17 related factor that was significantly associated with the response of patients with metastatic colorectal cancer to bevacizumab. But this main significant result is highly dependent on one case which, if left out, weakens the data. Other clinical studies are required to confirm this association.

trial registrationNCT00489697 . June 20, 2007.

Indexed as

Genetic Predisposition to DiseaseAgedBevacizumabColorectal NeoplasmsDisease-Free SurvivalFemaleGenetic Association StudiesHumansInterleukin-17MaleMiddle AgedNeoplasm MetastasisPolymorphism, Single NucleotideBevacizumabIL17A protein, humanInterleukin-17BevacizumabIL-17 polymorphismsMetastatic colorectal cancerSurvival analysis: scoreTh17-related cytokinesVascular endothelial growth factor

Identifiers

PMID28347290
PMCPMC5368920
OpenAlexW2600115309

What OpenQuestion holds

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Registered trials

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.