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. 2022 Nov;29(6):985-992.
doi: 10.1007/s12282-022-01378-6. Epub 2022 Jun 22.

Clinicopathological features of male patients with breast cancer based on a nationwide registry database in Japan

Affiliations

Clinicopathological features of male patients with breast cancer based on a nationwide registry database in Japan

Akihiko Shimomura et al. Breast Cancer. 2022 Nov.

Abstract

Background: Male breast cancer (MBC) is rare; however, its incidence is increasing. There have been no large-scale reports on the clinicopathological characteristics of MBC in Japan.

Methods: We investigated patients diagnosed with breast cancer in the Japanese National Clinical Database (NCD) between January 2012 and December 2018.

Results: A total of 594,316 cases of breast cancer, including 3780 MBC (0.6%) and 590,536 female breast cancer (FBC) (99.4%), were evaluated. The median age at MBC and FBC diagnosis was 71 (45-86, 5-95%) and 60 years (39-83) (p < 0.001), respectively. MBC cases had a higher clinical stage than FBC cases: 7.4 vs. 13.3% stage 0, 37.2 vs. 44.3% stage I, 25.6 vs. 23.9% stage IIA, 8.8 vs. 8.4% stage IIB, 1.9 vs. 2.4% stage IIIA, 10.1 vs. 3.3% stage IIIB, and 1.1 vs. 1.3% stage IIIC (p < 0.001). Breast-conserving surgery was more frequent in FBC (14.6 vs. 46.7%, p = 0.02). Axillary lymph node dissection was more frequent in MBC cases (32.9 vs. 25.2%, p < 0.001). Estrogen receptor(ER)-positive disease was observed in 95.6% of MBC and 85.3% of FBC cases (p < 0.001). The HER2-positive disease rates were 9.5% and 15.7%, respectively (p < 0.001). Comorbidities were more frequent in MBC (57.3 vs. 32.8%) (p < 0.001). Chemotherapy was less common in MBC, while endocrine therapy use was similar in ER-positive MBC and FBC. Perioperative radiation therapy was performed in 14.3% and 44.3% of cases.

Conclusion: Japanese MBC had an older age of onset, were more likely to be hormone receptor-positive disease, and received less perioperative chemotherapy than FBC.

Keywords: Japanese; Male breast cancer; National clinical database.

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Conflict of interest statement

Dr. Shimomura reports grants and personal fees from Chugai Pharmaceutical, grants and personal fees from AstraZeneca, grants and personal fees from Daiichi Sankyo, grants and personal fees from EISAI, grants from Taiho Pharmaceutical, grants from Mochida Pharmaceutical, personal fees from Pfizer, personal fees from Novartis, personal fees from Eli-Lilly, personal fees from Kyowa Kirin, personal fees from Takeda Pharmaceutical, and personal fees from MSD outside the submitted work. Dr. Kumamaru reports consulting fees from Mitsubishi-Tanabe Pharma, personal fees from Johnson and Johnson, personal feesl from Pfizer, personal fees from Chugai Pharmaceutical outside the submitted work, affiliated with the department of Healthcare Quality Assessment at the University of Tokyo supported by National Clinical Dabatase, Johnson & Johnson, and Nipro. Dr. Hayashi reports personal fees from AstraZeneca, personal fees from Taiho Pharmaceutical, personal fees from EISAI, personal fees from Exact Science, personal fees from Eli-Lilly, personal fees from Daiichi Sankyo, personal fees from Novartis, personal fees from Pfizer, personal fees from Chugai Pharmaceutical outside the submitted work. Dr. Miyata reports grants from affiliation of social collaboration department of National Clinical Database, Johnson and Johnson, and Nipro. Dr. Yamamoto reports personal fees from AstraZeneca, grants and personal fees from Chugai Pharmaceutical, grants and personal fees from Kyowa Kirin, personal fees from Novartis, grants and personal fees from EISAI, grants and personal fees from Daiichi Sankyo, grants and personal fees from Nippon Kayaku, grants and personal fees from Taiho Pharmaceutical, grants and personal fees from Takeda, grants and personal fees from Eli-Lilly, grants and personal fees from Pfizer, personal fees from Taiho Pharmaceutical, personal fees from Sysmex, personal fees from MSD outside the submitted work. Dr. Imoto reports grants from Taiho Pharmaceutical, grants from Daiichi Sankyo, grants from Eli-Lilly outside the submitted work. The other authors declare no potential conflicts of interest.

Figures

Fig. 1
Fig. 1
Distribution of each subtype in MBC (a) and FBC (b)

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