Evidence map›Paper›PMID 38619618›Full record

ArticleMedical molecular morphology2024

Utility of human epidermal growth factor 2 heterogeneity as a prognostic factor in triple-negative breast cancer.

Eriko Narusawa, Sasagu Kurozumi, Ayaka Katayama, Yukio Koibuchi, Akira Ogawa, Daisuke Takata, Shoko Tokuda, Sayaka Obayashi, Tetsunari Oyama, Jun Horiguchi and 2 more

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Article in Medical molecular morphology, 2024. 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. Article
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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

12 authors.

Eriko NarusawaDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Gunma, Japan.ORCID http://orcid.org/0009-0009-3896-2823
Sasagu KurozumiDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Gunma, Japan. skurozumi@iuhw.ac.jp.
Ayaka KatayamaDepartment of Diagnostic Pathology, Gunma University Graduate School of Medicine, Gunma, Japan.
Yukio KoibuchiDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Gunma, Japan.
Akira OgawaDepartment of Diagnostic Pathology, National Hospital Organization Takasaki General Medical Center, Gunma, Japan.
Daisuke TakataDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Gunma, Japan.
Shoko TokudaDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Gunma, Japan.
Sayaka ObayashiDepartment of General Surgical Science, Gunma University Graduate School of Medicine, Gunma, Japan.
Tetsunari OyamaDepartment of Diagnostic Pathology, Gunma University Graduate School of Medicine, Gunma, Japan.
Jun HoriguchiDepartment of Breast Surgery, International University of Health and Welfare, 852, Hatakeda, Narita City, Chiba, 286-8520, Japan.
Ken ShirabeDepartment of General Surgical Science, Gunma University Graduate School of Medicine, Gunma, Japan.
Takaaki FujiiDepartment of General Surgical Science, Gunma University Graduate School of Medicine, Gunma, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In some cases of human epidermal growth factor 2 (HER2)-negative breast cancer, including triple-negative breast cancer, HER2 expression is sporadically and strongly upregulated, a condition known as HER2 heterogeneity. We investigated the clinicopathological features of patients with HER2 heterogeneity in triple-negative breast cancers treated with neoadjuvant chemotherapy. Thirty-nine patients with triple-negative breast cancer who had undergone preoperative chemotherapy participated in this study. To assess for HER2 heterogeneity, we used dual in situ hybridization slides. We evaluated the association between HER2 heterogeneity and clinicopathological factors such as rates of pathologic complete response (pCR) and of recurrence-free survival. Of the 39 patients, 15 (38.5%) had cancers with HER2 heterogeneity. The pCR rates were 13.3% among patients with HER2 heterogeneity and 20.8% among those with HER2 nonheterogeneity, but the difference was not significant. The recurrence-free survival rate was significantly lower in patients with HER2 heterogeneity than in those without (P = 0.025). HER2 heterogeneity is a significant predictor of poor prognosis in patients with triple-negative breast cancer treated with neoadjuvant chemotherapy.

Indexed as

Erb-b2 Receptor Tyrosine KinasesNeoadjuvant TherapyTriple Negative Breast NeoplasmsAdultAgedBiomarkers, TumorDisease-Free SurvivalFemaleGenetic HeterogeneityHumansIn Situ HybridizationMiddle AgedPrognosisBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHeterogeneityPrognosisTriple-negative breast cancer

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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 OpenQuestion graph.