Evidence map›Paper›PMID 37856764›Full record

ArticleJCO precision oncology2023

Adoption of Universal Testing in Endometrial Cancers for Microsatellite Instability Using Next-Generation Sequencing.

Isabel V Rodriguez, Sarah Strickland, David Wells, Enna Manhardt, Eric Q Konnick, Rochelle Garcia, Elizabeth Swisher, Mark Kilgore, Barbara Norquist

Open access · greenAbstract read
In one paragraph

Article in JCO precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  4. Observational
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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

9 authors at 2 institutions in 2 countries.

Isabel V RodriguezDepartment of Obstetrics and Gynecology, University of Washington, Seattle, WA.ORCID 0000-0002-5113-6173
Sarah StricklandDepartment of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Canada.ORCID 0000-0002-9163-269X
David WellsDepartment of Pathology and Laboratory Medicine, University of Washington, Seattle, WA.
Enna ManhardtDepartment of Obstetrics and Gynecology, University of Washington, Seattle, WA.
Eric Q KonnickDepartment of Pathology and Laboratory Medicine, University of Washington, Seattle, WA.ORCID 0000-0001-5904-1788
Rochelle GarciaDepartment of Pathology and Laboratory Medicine, University of Washington, Seattle, WA.
Elizabeth SwisherDepartment of Obstetrics and Gynecology, University of Washington, Seattle, WA.
Mark KilgoreDepartment of Pathology and Laboratory Medicine, University of Washington, Seattle, WA.ORCID 0000-0001-9276-9359
Barbara NorquistDepartment of Obstetrics and Gynecology, University of Washington, Seattle, WA.ORCID 0000-0001-5992-7845
University of Washington · USUniversity of Ottawa · CA

Funding

TRAINING IN CANCER BIOLOGY &TRANSPLANTATIONT32CA009515 · NCI · UNIVERSITY OF WASHINGTON · PI NANCY ELLEN DAVIDSON, Effie W Petersdorf · 1985 to 2026
$16.2M
NCI NIH HHS T32 CA009515
6 · The paper itself

Abstract

purposeTo assess implementation of a next-generation sequencing (NGS) assay to detect microsatellite instability (MSI) as a screen for Lynch syndrome (LS) in endometrial cancer (EC), while determining and comparing characteristics of the four molecular subtypes.

methodsA retrospective review was performed of 408 total patients with newly diagnosed EC: 140 patients who underwent universal screening with NGS and 268 patients who underwent screening via mismatch repair immunohistochemistry (MMR IHC) as part of a historical screening paradigm. In the NGS cohort, incidental

resultsIn the NGS cohort, 38 subjects (27%) had MSI-H EC, 100 (71%) had microsatellite stable EC, and two (1%) had an indeterminate result. LS was diagnosed in two subjects (1%), and all but five patients completed genetic screening (96%). Molecular subtypes were ascertained: eight had

conclusionMSI by NGS allowed for simultaneous screening for LS and categorization of EC into molecular subtypes with prognostic and therapeutic implications.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisEndometrial NeoplasmsFemaleGenetic TestingHigh-Throughput Nucleotide SequencingHumansMicrosatellite InstabilityMutation

Identifiers

PMID37856764
PMCPMC10861015
OpenAlexW4387786011

What OpenQuestion holds

Textmetadata
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.