Evidence map›Paper›PMID 36672477›Full record

ArticleCancers2023

Association of Genomic Instability Score, Tumor Mutational Burden, and Tumor-Infiltrating Lymphocytes as Biomarkers in Uterine Serous Carcinoma.

Elizabeth A Bloom, Pamela N Peters, Regina Whitaker, Shonagh Russell, Benjamin Albright, Shelly Cummings, Kirsten M Timms, Thomas Slavin, Braden Probst, Kyle C Strickland and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 1 country.

Elizabeth A BloomDuke University School of Medicine, Duke University, Durham, NC 27710, USA.ORCID 0000-0003-2854-7529
Pamela N PetersDepartment of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University School of Medicine, Durham, NC 27710, USA.
Regina WhitakerDepartment of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University School of Medicine, Durham, NC 27710, USA.
Shonagh RussellDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0003-1066-6132
Benjamin AlbrightDepartment of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University School of Medicine, Durham, NC 27710, USA.
Shelly CummingsMyriad Genetics Laboratories, Inc., Salt Lake City, UT 84108, USA.
Kirsten M TimmsMyriad Genetics Laboratories, Inc., Salt Lake City, UT 84108, USA.
Thomas SlavinMyriad Genetics Laboratories, Inc., Salt Lake City, UT 84108, USA.
Braden ProbstMyriad Genetics Laboratories, Inc., Salt Lake City, UT 84108, USA.
Kyle C StricklandDepartment of Pathology, Duke University, Durham, NC 27708, USA.
Rebecca A PrevisDepartment of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University School of Medicine, Durham, NC 27710, USA.ORCID 0000-0001-8087-9120
Duke University · USMyriad Genetics · US

Funding

Duke Women's Reproductive Health Research ScholarsK12HD103083 · NICHD · DUKE UNIVERSITY · PI Cindy Amundsen · 2020 to 2026
$2.2M
Understanding metabolic vulnerabilities in cancer and the impact the tumor microenvironment has on cancer progression.K00CA234942 · NCI · DUKE UNIVERSITY · PI RUSSELL, SHONAGH · 2020 to 2023
$366k
NCI NIH HHS K00 CA234942NICHD NIH HHS K12 HD103083NIH HHS NIH 1K12HD103083-01
6 · The paper itself

Abstract

Background: Uterine serous carcinomas represent 10% of uterine carcinomas but account for nearly 40% of deaths from the disease. Improved molecular characterization of these tumors is instrumental in guiding targeted treatment and improving outcomes. This study assessed the genomic instability score (GIS), tumor mutational burden (TMB), and tumor-infiltrating lymphocytes (TILs) in patients with USC. Methods: A retrospective cohort study evaluated patients with USC following staging surgery. The GIS and TMB were determined from archived specimens. We evaluated the tumoral expression of CD3, CD4, CD8, FOXP3, and CD68 using immunohistochemistry. T-tests were used to assess associations of TILs with the GIS. Results: We evaluated 53 patients with USC. The median GIS was 31 (range: 0−52) and a higher GIS was not associated with progression-free (PFS) or overall survival (OS). The median TMB was 1.35 mt/Mb; patients with TMB > 1.35 mt/Mb had improved PFS and OS (p = 0.005; p = 0.002, respectively). Tumors with increased CD3+ and CD4+ immune cells had a higher mean GIS (p = 0.013, p = 0.002). Conclusions: TMB > 1.35 mt/Mb was associated with improved survival in USC patients, whereas the GIS was not. Lower TMB thresholds may provide prognostic value for less immunogenic tumors such as USC. In this limited cohort, we observed that increased TIL populations were correlated with a higher GIS.

Indexed as

genomic instabilityimmunohistochemistrytumor-infiltrating lymphocytestumor mutational burdenuterine serous cancer

Identifiers

PMID36672477
PMCPMC9856872
OpenAlexW4316664440

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.