Evidence map›Paper›PMID 29158497›Full record

SynthesisNature communications2017

Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women.

Latha Kadalayil, Sofia Khan, Heli Nevanlinna, Peter A Fasching, Fergus J Couch, John L Hopper, Jianjun Liu, Tom Maishman, Lorraine Durcan, Sue Gerty and 6 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Nature communications, 2017. 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
2.0field-weighted citation impact, top 12% 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, 30 citations in OpenAlex.

  1. Pooled it
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  16. A Ten-NFrontiers in oncology · 2020
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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

16 authors at 10 institutions in 6 countries.

Latha KadalayilGenetic Epidemiology and Bioinformatics Research Group, Human Development and Health Academic Unit, Faculty of Medicine, Duthie Building (MP 808), University of Southampton, Southampton General Hospital, Southampton, SO16 6YD, UK.
Sofia KhanDepartment of Obstetrics and Gynaecology, University of Helsinki and Helsinki University Hospital, Helsinki, P.O. BOX 700, 00029 HUS, Finland.
Heli NevanlinnaDepartment of Obstetrics and Gynaecology, University of Helsinki and Helsinki University Hospital, Helsinki, P.O. BOX 700, 00029 HUS, Finland.ORCID http://orcid.org/0000-0002-0916-2976
Peter A FaschingUniversity Breast Center Franconia, Department of Gynaecology and Obstetrics, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Comprehensive Cancer Center Erlangen-EMN, 91054, Erlangen, Germany.
Fergus J CouchDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, 55901, USA.
John L HopperCentre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, 3010, Australia.
Jianjun LiuHuman Genetics, Genome Institute of Singapore, 60 Biopolis Street, Singapore, 138672, Singapore.
Tom MaishmanSouthampton Clinical Trials Unit, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK.
Lorraine DurcanSouthampton Clinical Trials Unit, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK.
Sue GertySouthampton Clinical Trials Unit, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK.
Carl BlomqvistDepartment of Oncology, Helsinki University Central Hospital, P.O. Box 180, FIN-00029, Helsinki, Finland.
Brigitte RackDepartment of Gynecology and Obstetrics, University Ulm, Prittwitzstrasse 43, 89075, Ulm, Germany.
Wolfgang JanniDepartment of Gynecology and Obstetrics, University Ulm, Prittwitzstrasse 43, 89075, Ulm, Germany.
Andrew CollinsGenetic Epidemiology and Bioinformatics Research Group, Human Development and Health Academic Unit, Faculty of Medicine, Duthie Building (MP 808), University of Southampton, Southampton General Hospital, Southampton, SO16 6YD, UK.
Diana EcclesCancer Sciences Division, Faculty of Medicine, University of Southampton, Southampton University Hospitals NHS Trust, Southampton, SO16 6YD, UK.
William TapperGenetic Epidemiology and Bioinformatics Research Group, Human Development and Health Academic Unit, Faculty of Medicine, Duthie Building (MP 808), University of Southampton, Southampton General Hospital, Southampton, SO16 6YD, UK. W.J.Tapper@soton.ac.uk.
Southampton General Hospital · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversität Ulm · DEUniversity of Helsinki · FIHelsinki University Hospital · FIMayo Clinic · USNational University of Singapore · SGThe University of Melbourne · AUUniversitätsklinikum Erlangen · DEUniversity of Southampton · GB

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI Fergus Joseph Couch · 2005 to 2026
$49.9M
NCI NIH HHS P50 CA116201
6 · The paper itself

Abstract

To identify genetic variants associated with breast cancer prognosis we conduct a meta-analysis of overall survival (OS) and disease-free survival (DFS) in 6042 patients from four cohorts. In young women, breast cancer is characterized by a higher incidence of adverse pathological features, unique gene expression profiles and worse survival, which may relate to germline variation. To explore this hypothesis, we also perform survival analysis in 2315 patients aged ≤ 40 years at diagnosis. Here, we identify two SNPs associated with early-onset DFS, rs715212 (P

Indexed as

Germ-Line MutationADAMTS ProteinsAdolescentAdultAgedAged, 80 and overAmphiregulinAntineoplastic AgentsBreast NeoplasmsDisease-Free SurvivalExtracellular Matrix ProteinsFemaleGenome-Wide Association StudyHumansMiddle AgedPolymorphism, Single NucleotideADAMTSL1 protein, humanADAMTS ProteinsAmphiregulinAntineoplastic AgentsAREG protein, humanExtracellular Matrix Proteins

Identifiers

PMID29158497
PMCPMC5696339
OpenAlexW2769201183

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.