Evidence map›Paper›PMID 27764800›Full record

ArticleOncotarget2016

GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.

David G Cox, Elsa Curtit, Gilles Romieu, Pierre Fumoleau, Maria Rios, Hervé Bonnefoi, Thomas Bachelot, Patrick Soulié, Christelle Jouannaud, Hugues Bourgeois and 25 more

Registry-linked trialOpen access · diamondAbstract readMulticenter Study
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00381901 (Protocol of Herceptin Adjuvant With Reduced Exposure, a Randomised Comparison of 6 Months vs 12 Months in All Women Receiving Adjuvant Herceptin [PHARE]), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 19% 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.

NCT00381901 phase3completednot on this map

Protocol of Herceptin Adjuvant With Reduced Exposure, a Randomised Comparison of 6 Months vs 12 Months in All Women Receiving Adjuvant Herceptin [PHARE]

TypeinterventionalSponsorNational Cancer Institute, FranceRan2006Enrolled3,400ConditionsBreast CancerArmstrastuzumab, polymorphism analysis, adjuvant therapy
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. LowerBiology · 2024
    Article
  2. Article
  3. Article
  4. Fibroblast growth factor receptor 2 gene (Saudi journal of biological sciences · 2021
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Fibroblast Growth Factor Receptor 2 Signaling in Breast Cancer.International journal of biological sciences · 2017
    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

35 authors at 20 institutions in 1 country.

David G CoxCentre de Recherche en Cancérologie de Lyon, INSERM U1052 - Centre Léon Bérard, 69373 Lyon, France.
Elsa CurtitHôpital Jean-Minjoz, Centre Hospitalier Universitaire, Boulevard Fleming, 25030 Besançon, France.
Gilles RomieuOncologie Sénologie, ICM Institut Régional du Cancer, 34298 Montpellier Cedex, France.
Pierre FumoleauGeorges-François Leclerc, 21000 Dijon, France.
Maria RiosInstitut de Cancérologie de Lorraine - Alexis Vautrin, Département d'Oncologie Médicale, 54511 Vandœuvre-lès-Nancy Cedex, France.
Hervé BonnefoiInstitut Bergonié, Département d'Oncologie Médicale, 33000 Bordeaux, France.
Thomas BachelotCentre Léon Bérard, Département de Cancérologie Médicale, Lyon Cedex 08, France.
Patrick SouliéInstitut de Cancérologie de l'Ouest, Service Oncologie Médicale, 49993 Angers Cedex 09, France.
Christelle JouannaudInstitut Jean Godinot, Service Oncologie Médicale, 51056 Reims Cedex, France.
Hugues BourgeoisClinique Victor Hugo-Centre Jean Bernard, 72015 Le Mans Cedex 2, France.
Thierry PetitCentre Paul Strauss, Service d'Oncologie Médicale, 67065 Strasbourg Cedex, France.
Isabelle TennevetCentre Henri Becquerel, rue d'Amiens, 76038 Rouen, France.
David AssoulineInstitut Daniel Hollard, Service Oncologie Médicale, 38028 Grenoble Cedex 01, France.
Marie-Christine MathieuInstitut Gustave Roussy, Comité de Pathologie Mammaire, 94805 Villejuif Cedex, France.
Jean-Philippe JacquinInstitut de Cancérologie Lucien Neuwirth, Service Oncologie Médicale, 42270 Saint Priest en Jarez, France.
Sandrine Lavau-DenesCentre Hospitalier de Limoges, Service d'Oncologie Médicale, 87042 Limoges Cedex, France.
Ariane Darut-JouveClinique Drévon, Centre d'Oncologie et de Radiothérapie du Parc, 21000 Dijon, France.
Jean-Marc FerreroCentre Antoine Lacassagne, Département Oncologie Médicale, 06189 Nice Cedex 02, France.
Carole TarpinInstitut Paoli-Calmettes, Département d'Oncologie Médicale, 13009 Marseille, France.
Christelle LévyCentre François Baclesse, 14076 Caen Cedex 5, France.
Valérie DelecroixPôle Mutualiste, Service Oncologie Médicale, 44606 Saint Nazaire, France.
Véronique Trillet-LenoirCentre Hospitalier Lyon Sud, Service d'Oncologie Médicale, 69495 Pierre-Benite cedex, France.
Oana CojocarasuCentre Hospitalier Le Mans, Service d'Onco-Hématologie et Médecine interne, 72037 Le Mans Cedex, France.
Jérôme MeunierCentre Hospitalier Régional d'Orléans, Service d'Oncologie Médicale, 45032 Orleans Cedex 1, France.
Jean-Yves PiergaInstitut Curie, Department of Medical Oncology, 75248 Paris Cedex 05, France.
Céline Faure-MercierInstitut National du Cancer, Direction de la Recherche, 92513 Boulogne-Billancourt, France.
Hélène BlanchéFondation Jean Dausset, Centre d'Etudes du Polymorphisme Humain, 75010 Paris, France.
Mourad SahbatouFondation Jean Dausset, Centre d'Etudes du Polymorphisme Humain, 75010 Paris, France.
Anne BolandCentre National du Génotypage, Institut de Génomique, CEA, CP 5721, 91057 Evry Cedex, France.
Delphine BacqCentre National du Génotypage, Institut de Génomique, CEA, CP 5721, 91057 Evry Cedex, France.
Céline BesseCentre National du Génotypage, Institut de Génomique, CEA, CP 5721, 91057 Evry Cedex, France.
Jean-François DeleuzeFondation Jean Dausset, Centre d'Etudes du Polymorphisme Humain, 75010 Paris, France.
Iris PauportéInstitut National du Cancer, Direction de la Recherche, 92513 Boulogne-Billancourt, France.
Gilles ThomasSynergie Lyon Cancer, Centre Léon Bérard, Lyon Cedex 08, France.
Xavier PivotHôpital Jean-Minjoz, Centre Hospitalier Universitaire, Boulevard Fleming, 25030 Besançon, France.
Fondation Jean Dausset-CEPH · FRCentre Hospitalier Universitaire de Besançon · FRCentre Léon Bérard · FRGenoscope · FRInstitut National du Cancer · FRCentre Antoine Lacassagne · FRCentre François Baclesse · FRCentre Georges François Leclerc · FRCentre Henri BecquerelCentre Hospitalier du Mans · FRCentre hospitalier régional d'Orléans · FRCentre Hospitalier Universitaire de Limoges · FRCentre Jean Bernard · FRClinique Mutualiste de l'Estuaire · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRHôpital Lyon Sud · FRInserm · FRInstitut Bergonié · FRInstitut Curie · FRInstitut de Cancérologie de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic polymorphisms are associated with breast cancer risk. Clinical and epidemiological observations suggest that clinical characteristics of breast cancer, such as estrogen receptor or HER2 status, are also influenced by hereditary factors. To identify genetic variants associated with pathological characteristics of breast cancer patients, a Genome Wide Association Study was performed in a cohort of 9365 women from the French nationwide SIGNAL/PHARE studies (NCT00381901/RECF1098). Strong association between the FGFR2 locus and ER status of breast cancer patients was observed (ER-positive n=6211, ER-negative n=2516; rs3135718 OR=1.34 p=5.46×10-12). This association was limited to patients with HER2-negative tumors (ER-positive n=4267, ER-negative n=1185; rs3135724 OR=1.85 p=1.16×10-11). The FGFR2 locus is known to be associated with breast cancer risk. This study provides sound evidence for an association between variants in the FGFR2 locus and ER status among breast cancer patients, particularly among patients with HER2-negative disease. This refinement of the association between FGFR2 variants and ER-status to HER2-negative disease provides novel insight to potential biological and clinical influence of genetic polymorphisms on breast tumors.

Indexed as

Biomarkers, TumorGenome-Wide Association StudyBreast NeoplasmsClinical Trials, Phase III as TopicCohort StudiesErb-b2 Receptor Tyrosine KinasesFemaleGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideRandomized Controlled Trials as TopicReceptor, Fibroblast Growth Factor, Type 2Receptors, EstrogenBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesFGFR2 protein, humanReceptor, Fibroblast Growth Factor, Type 2Receptors, Estrogenassociationbreastestrogen receptorGWASHER2

Identifiers

PMID27764800
PMCPMC5363591
OpenAlexW2530258008

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.