Evidence map›Paper›PMID 40117942›Full record

ReviewGynecologic oncology2025

Diagnostic and therapeutic advances for HER2-expressing or amplified gynecologic cancers.

Elizabeth K Lee, David L Kolin, Ursula A Matulonis, Britt K Erickson

Abstract readReview
In one paragraph

Review in Gynecologic oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. 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

4 authors.

Elizabeth K LeeDivision of Gynecologic Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States of America. Electronic address: elizabethk_lee@dfci.harvard.edu.
David L KolinDepartment of Pathology, Brigham & Women's Hospital, Boston, MA, United States of America.
Ursula A MatulonisDivision of Gynecologic Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States of America.
Britt K EricksonDivision of Gynecologic Oncology, Department of Obstetrics & Gynecology, University of Minnesota, Minneapolis, MN, United States of America.

Funding

Increasing access to cancer trials in Minnesota (InACT-MN)R50CA278811 · NCI · UNIVERSITY OF MINNESOTA · PI Britt Kristina Erickson · 2023 to 2026
$731k
NCI NIH HHS R50 CA278811
6 · The paper itself

Abstract

HER2-targeting therapies are well-described in breast, gastric, and lung cancers, however accumulating data supports a role for HER2-targeted therapies in gynecologic cancers. Despite varied methodologies for HER2 testing, evidence supports that a substantial proportion of endometrial, ovarian, cervical, and vulvar cancers overexpress HER2. This underscores the rationale for HER2-targeted therapies in these malignancies, including the use of HER2-directed tyrosine kinase inhibitors, antibody-drug conjugates, and immune-stimulating antibody conjugates. Understanding mechanisms of resistance to HER2-targeted therapies will inform possible combinatorial strategies.

Indexed as

Erb-b2 Receptor Tyrosine KinasesGenital Neoplasms, FemaleFemaleHumansImmunoconjugatesMolecular Targeted TherapyProtein Kinase InhibitorsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmunoconjugatesProtein Kinase InhibitorsAntibody drug conjugateBiomarker testingHer2Therapeutic antibodyTyrosine kinase inhibitor

Identifiers

PMID40117942
PMCPMC12248254

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.