Evidence map›Paper›PMID 34083606›Full record

ArticleScientific reports2021

Lost opportunities for mismatch repair (MMR) screening among minority women with endometrial cancer.

Marilyn Huang, Tegan Hunter, Lydia A Fein, Johnny Galli, Sophia George, Matthew Schlumbrecht, Kelly McCarter, Abdulrahman K Sinno, Luiz P Guido, Andre Pinto

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. 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
0.9field-weighted citation impact, top 27% 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, 6 citations in OpenAlex.

  1. Article
  2. Racioethnic Disparities in Endometrial Cancer Outcomes.Diagnostics (Basel, Switzerland) · 2024
    Review
  3. Article
  4. 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

10 authors at 2 institutions in 1 country.

Marilyn HuangDivision of Gynecologic Oncology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1121 NW 14th St, Suite 345E, Miami, FL, 33136, USA. m.huang@med.miami.edu.
Tegan HunterUniversity of Miami Miller School of Medicine, 1600 NW 10th Avenue, Miami, FL, 33136, USA.
Lydia A FeinDepartment of Obstetrics, Gynecology and Reproductive Medicine, University of Miami Miller School of Medicine, 1120 NW 14th Street, Miami, FL, 33136, USA.
Johnny GalliDepartment of Obstetrics, Gynecology and Reproductive Medicine, University of Miami Miller School of Medicine, 1120 NW 14th Street, Miami, FL, 33136, USA.
Sophia GeorgeDivision of Gynecologic Oncology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1121 NW 14th St, Suite 345E, Miami, FL, 33136, USA.
Matthew SchlumbrechtDivision of Gynecologic Oncology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1121 NW 14th St, Suite 345E, Miami, FL, 33136, USA.
Kelly McCarterUniversity of Miami Miller School of Medicine, 1600 NW 10th Avenue, Miami, FL, 33136, USA.
Abdulrahman K SinnoDivision of Gynecologic Oncology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1121 NW 14th St, Suite 345E, Miami, FL, 33136, USA.
Luiz P GuidoDepartment of Pathology, University of Miami Miller School of Medicine, 1120 NW 14th Street, Miami, FL, 33136, USA.
Andre PintoDepartment of Pathology, University of Miami Miller School of Medicine, 1120 NW 14th Street, Miami, FL, 33136, USA.
University of Miami · USSylvester Comprehensive Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lynch Syndrome (LS) prevalence in underrepresented minorities are lacking. The objective of this study was to assess the prevalence of LS in a minority patient population. Secondary objectives included identifying factors associated with successful LS screening and to characterize clinicopathologic features. Women with endometrial cancer treated within a university system from 2014 and 2016 were included. Immunohistochemistry (IHC) results of MLH1, PMS2, MSH2 and MSH6 were obtained from medical records and clinicopathologic factors abstracted. Patients not previously screened for LS were screened. 276 patients were evaluable. More minority women were screened as part of their routine cancer care (p = 0.005). Additionally, women 50 years or younger were more likely to be screened for LS compared to women older than 51(p = 0.009) and uninsured or reliant on Medicaid patients (p = 0.011) were more likely to be screened during routine care. Six patients received confirmatory germline testing for LS (4.3%), and another 8 patients had a staining pattern suggestive of LS. In an underrepresented population, the rate of LS in endometrial cancer is similar to previous reports. LS may be under diagnosed and opportunities missed when universal screening is not applied in minority women.

Indexed as

DNA Mismatch RepairMinority GroupsAdultAgedBiomarkers, TumorEarly Detection of CancerEndometrial NeoplasmsFemaleGenetic CounselingGenetic Predisposition to DiseaseHumansImmunohistochemistryMass ScreeningMiddle AgedBiomarkers, Tumor

Identifiers

PMID34083606
PMCPMC8175729
OpenAlexW3165098283

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.