Evidence map›Paper›PMID 36494460›Full record

ArticleBreast cancer research and treatment2023

Clinicopathological features, genetic alterations, and BRCA1 promoter methylation in Japanese male patients with breast cancer.

Akihiko Shimomura, Masayuki Yoshida, Takashi Kubo, Satoshi Yamashita, Emi Noguchi, Aiko Nagayama, Toru Hanamura, Miki Okazaki, Toru Mukohara, Asako Tsuruga and 9 more

Abstract read
In one paragraph

Article in Breast cancer research and treatment, 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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. 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

19 authors.

Akihiko ShimomuraDepartment of Breast and Medical Oncology, National Center for Global Health and Medicine, 1-21-1 Toyama, Shinjuku-Ku, Tokyo, 162-8655, Japan. akshimomura@hosp.ncgm.go.jp.ORCID http://orcid.org/0000-0002-2557-8170
Masayuki YoshidaDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Takashi KuboDepartment of Clinical Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Satoshi YamashitaDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Emi NoguchiDepartment of Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Aiko NagayamaDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.
Toru HanamuraDepartment of Breast Oncology, Tokai University School of Medicine, Kanagawa, Japan.
Miki OkazakiDepartment of Breast Oncology, Tokyo Medical University, Tokyo, Japan.
Toru MukoharaDepartment of Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Asako TsurugaDivision of Breast Surgical Oncology, Department of Surgery, Showa University Hospital, Tokyo, Japan.
Kiyo TanakaDepartment of Breast and Endocrine Surgery, Toranomon Hospital, Tokyo, Japan.
Yukino KawamuraDepartment of Breast and Medical Oncology, National Center for Global Health and Medicine, 1-21-1 Toyama, Shinjuku-Ku, Tokyo, 162-8655, Japan.
Toru HiguchiBreast Unit, Japanese Red Cross Saitama Hospital, Saitama, Japan.
Yoko TakahashiDepartment of Breast Surgical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Sasagu KurozumiDepartment of Breast Surgery, International University of Health and Welfare, Chiba, Japan.
Tetsu HayashidaDepartment of Surgery, Keio University School of Medicine, Tokyo, Japan.
Hitoshi IchikawaDepartment of Clinical Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Toshikazu UshijimaDivision of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan.
Akihiko SutoDepartment of Breast Surgery, National Cancer Center Hospital, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMale breast cancer (MBC) is a rare cancer accounting for only 1% of all male cancers and is, therefore, poorly studied. We aimed to characterize the subtypes of MBC in Japanese patients based on genetic profiling, the presence of tumor-infiltrating cells, and the expression of immunohistochemical markers.

methodsThis retrospective study included 103 patients with MBC diagnosed between January 2009 and December 2019 at various hospitals in Japan. Clinicopathological patient characteristics were obtained from medical records, and formalin-fixed paraffin-embedded tissue specimens were analyzed for histological markers, mutations of 126 genes, BRCA1 methylation, and stromal tumor-infiltrating lymphocytes.

resultsThe median patient age was 71 (range 31-92) years. T1-stage tumors were the most frequent (47.6%), and most were node negative (77.7%). The majority of tumors were positive for estrogen receptor (98.1%), progesterone receptor (95.1%), and androgen receptor (96.1%), and BRCA2 was the most frequently mutated gene (12.6%). The most common treatment was surgery (99.0%), either total mastectomy (91.1%) or partial mastectomy (7.0%). Survival analysis showed a 5-year recurrence-free survival rate of 64.4% (95% confidence interval [CI] 46.7-88.8) and a 5-year overall survival rate of 54.3% (95% CI 24.1-100.0).

conclusionJapanese MBC is characterized by a high rate of hormonal receptor positivity and BRCA2 somatic mutation. Due to the observed clinicopathological differences in MBC between the Western countries and Japan, further prospective studies are needed to evaluate the most suitable treatment strategies.

Indexed as

Breast NeoplasmsBreast Neoplasms, MaleAdultAgedAged, 80 and overBRCA1 ProteinBRCA2 ProteinEast Asian PeopleHumansMaleMastectomyMethylationMiddle AgedMutationRetrospective StudiesBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBiomarkersDescriptive studiesMale breast cancerRare cancersTranslational research

Identifiers

PMID36494460
PMCPMC9883318

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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.