Evidence map›Paper›PMID 42548619›Full record

ArticleFrontiers in oncology2026

Association between HER2 expression, genomic characteristics, and tumor immune microenvironment dynamics in epithelial ovarian cancer.

Julia Salinaro, Payton De La Cruz, Shriya Perati, Julia McAdams, Samantha Buyungo, Janina Pearce, Areta Bojko, Angelica Salaverria, Kamaljeet Singh, Paul DiSilvestro and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Julia SalinaroProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Payton De La CruzProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Shriya PeratiDepartment of Obstetrics and Gynecology, Warren-Alpert Medical School of Brown University, Providence, RI, United States.
Julia McAdamsProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Samantha BuyungoProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Janina PearceProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Areta BojkoProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Angelica SalaverriaTherapeutic Sciences Graduate Program, Brown University, Providence, RI, United States.
Kamaljeet SinghDepartment of Pathology, Women and Infants Hospital, Providence, RI, United States.
Paul DiSilvestroProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Cara MathewsProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.
Nicole E JamesProgram in Women's Oncology, Women and Infants Hospital, Providence, RI, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite the rapid clinical approval of the HER2-directed antibody-drug conjugate trastuzumab deruxtecan (T-DXd) for patients with HER2-expressing epithelial ovarian cancer (EOC), preclinical mechanistic studies are lacking.The goal of this investigation was to determine the genomic and immunogenic characteristics associated with HER2 expressing EOC in order to better understand the mechanism of treatment response and what subset of patients will benefit most from single agent and combinatorial HER2-directed treatment regimens. Methods: 130 EOC patients were retrospectively identified from our institution's internal clinical genomic database. Selected genomic characteristics were stratified by gastric HER2 score and distributions were analyzed by Fisher's exact test. A subset of 34 EOC tumors were internally HER2 stained and fluorescent immunohistochemistry analysis of PD-L1, CD4, and CD8 was performed. EOC cell lines were treated with T-DXd and Results: Non-significant differences were detected in HRD, Conclusions: HER2 high EOC tumors are more likely to be FOLR1 negative and PD-L1 positive, and treatment with T-DXd downregulates

Indexed as

epithelial ovarian cancerHER2PD-L1trastuzumab deruxtecanVEGF

Identifiers

PMID42548619
PMCPMC13429427

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.