Evidence mapPaperPMID 39937426Full record

ArticleInternational journal of clinical oncology2025

Human epidermal growth factor receptor 3 expression in patients with epithelial ovarian cancer: a potential target for ovarian mucinous and clear cell carcinoma.

Sho Sato, Daisuke Shintani, Yuki Kaneda, Ryuichi Nakamura, Tomomi Katoh, Mitsutake Yano, Mieko Hanaoka, Shigehiro Yagishita, Masanori Yasuda, Motoko Nagata and 1 more

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Article in International journal of clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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

11 authors.

Sho SatoDepartment of Gynecologic Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama, 350-1298, Japan.ORCID http://orcid.org/0000-0001-5628-7141
Daisuke ShintaniDepartment of Gynecologic Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama, 350-1298, Japan.ORCID http://orcid.org/0000-0001-6689-8915
Yuki KanedaTranslational Science Department I, Daiichi Sankyo Co., Ltd., Shinagawa, Tokyo, 140-8710, Japan.
Ryuichi NakamuraTranslational Science Department I, Daiichi Sankyo Co., Ltd., Shinagawa, Tokyo, 140-8710, Japan.
Tomomi KatohDepartment of Pathology, Saitama Medical University International Medical, Center, Hidaka, Saitama, 350-1298, Japan.
Mitsutake YanoDepartment of Pathology, Saitama Medical University International Medical, Center, Hidaka, Saitama, 350-1298, Japan.ORCID http://orcid.org/0000-0002-4436-838X
Mieko HanaokaDepartment of Gynecologic Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama, 350-1298, Japan.
Shigehiro YagishitaDivision of Molecular Pharmacology, National Cancer Center Research Institute, Tsukiji, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1277-1203
Masanori YasudaDepartment of Pathology, Saitama Medical University International Medical, Center, Hidaka, Saitama, 350-1298, Japan.ORCID http://orcid.org/0000-0002-0769-360X
Motoko NagataTranslational Science Department I, Daiichi Sankyo Co., Ltd., Shinagawa, Tokyo, 140-8710, Japan.ORCID http://orcid.org/0009-0006-2019-9100
Kosei HasegawaDepartment of Gynecologic Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama, 350-1298, Japan. koseih@saitama-med.ac.jp.ORCID http://orcid.org/0000-0002-1903-7001

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman epidermal growth factor receptor 3 (HER3), a tyrosine kinase belonging to the HER family, is a known target for cancer therapy; recently, an anti-HER3 antibody-drug conjugate (ADC) is developing. To understand HER3 expression in epithelial ovarian cancer (EOC), this study was conducted.

methodsWe investigated the expression of HER3 in 202 patients with EOC using immunohistochemistry (IHC), and the association between HER3 expression, clinicopathological features, prognosis, and treatment timing.

resultsOf all the cases, 55.4% had a HER3 IHC score ≥ 1 + . In particular, 78.0% of the patients with clear cell carcinoma (CCC) and 87.9% of the patients with mucinous carcinoma (MC) had a HER3 IHC score ≥ 1 + . Regarding clinicopathological features, early disease stage, feasibility of primary debulking surgery, no residual tumor, and low CA125 levels were more frequently observed in patients with a HER3 IHC score ≥ 1 + . Furthermore, a HER3 no-expression showed a significant association with a relatively short progression-free survival (PFS). And, for patients with mucinous carcinoma, those with a HER3 IHC score ≥ 1 + had poorer PFS and overall survival than those with a HER3 no-expression (no statistically significant difference). In addition, we analyzed HER3 expression at primary tumor and recurrence tumor in same patients. Thus, we observed the HER3 IHC score tended to change from 0 to ≥ 1 + in recurrence cases compared with primary cases.

conclusionsThese observations suggested that patients with MC, CCC and recurrence of all histological type may potentially benefit from future clinical trials of HER3-directed therapies.

Indexed as

Adenocarcinoma, Clear CellAdenocarcinoma, MucinousCarcinoma, Ovarian EpithelialOvarian NeoplasmsReceptor, ErbB-3AdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansImmunohistochemistryMiddle AgedPrognosisProgression-Free SurvivalBiomarkers, TumorERBB3 protein, humanReceptor, ErbB-3HER3IHCOvarian cancerOvarian clear cell carcinomaOvarian mucinous carcinomaPrognosis

Identifiers

PMID39937426

What Socratic holds

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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 Socratic graph.