Evidence map›Paper›PMID 33302456›Full record

Trial reportGenes2020

Heritability of Low ER Staining/HER2-Breast Tumors: Are We Missing an Opportunity for Germline Testing?

Leann A Lovejoy, Clesson E Turner, Justin M Wells, Craig D Shriver, Rachel E Ellsworth

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors at 4 institutions in 1 country.

Leann A LovejoyChan Soon-Shiong Institute for Molecular Medicine at Windber, Windber, PA 15963, USA.
Clesson E TurnerDepartment of Pediatrics, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Justin M WellsDepartment of Pathology, Walter Reed National Military Medical Center, Bethesda, MD 20814, USA.
Craig D ShriverDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.ORCID 0000-0001-8993-5811
Rachel E EllsworthMurtha Cancer Center/Research Program, Uniformed Services University of the Health Sciences and Walter Reed National Military Medical Center, Bethesda, MD 20814, USA.ORCID 0000-0003-2287-1635
Uniformed Services University of the Health Sciences · USHenry M. Jackson Foundation · USWalter Reed National Military Medical Center · USWindber Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2010, the genetic testing criteria was changed to allow women diagnosed ≤ 60 years old with triple negative breast cancer (TNBC) to undergo germline testing. In the same year, estrogen receptor (ER) positivity was defined as having ≥1% ER staining cells. While tumors with 1-10% ER staining cells and HER2 negative (HER2-) status share characteristics with TNBC, the utility of germline testing in women with ER low positive/HER2- (ERLP/HER2-) tumors is not well-understood. To this end, all patients with hormone receptor positive staining cells ≤ 10% and negative HER2 status were identified. Clinical genetic test results were extracted for patients who underwent testing. Panel testing was performed for those women who had genomic DNA available for research purposes. ERLP/HER2-tumors constituted 2.7% of all tumors in the database. Patients did not differ significantly from those with TNBC by age at diagnosis, ethnicity, family history or tumor size, stage or grade (

Indexed as

Erb-b2 Receptor Tyrosine KinasesGerm-Line MutationReceptors, EstrogenTriple Negative Breast NeoplasmsAdultFemaleHumansMiddle AgedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenASCO/CAP guidelinesbreast cancerER low positivegenetic testing

Identifiers

PMID33302456
PMCPMC7763582
OpenAlexW3111134841

What OpenQuestion holds

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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.