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Survival trends and patient characteristics between 2004 and 2016 for breast cancer in Japan based on the National Clinical Database-Breast Cancer Registry

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Abstract

This is a prognostic report by the Japanese Breast Cancer Society on breast cancer extracted from the National Clinical Database-Breast Cancer Registry of Japan. Here, we present a summary of 457,878 breast cancer cases registered between 2004 and 2016. The median follow-up duration was 5.6 years. The median age at the start of treatment was 59 years (5–95%: 38–82 years) and increased from 57 years between 2004 and 2008 to 60 years between 2013 and 2016. The proportion of patients with Stage 0–II disease increased from 74.5% to 78.3%. The number of cases with estrogen and progesterone receptor positivity increased from 74.8% to 77.9% and 60.5% to 68.1%, respectively. Regarding (neo-)adjuvant chemotherapy, the taxane (T) or taxane-cyclophosphamide (C) regimen increased by 2.4% to 8.2%, but the (fluorouracil (F)) adriamycin (A)-C-T/(F) epirubicin (E)C-T and (F)AC/(F)EC regimens decreased by 18.6% to 15.2% and 13.5% to 5.0%, respectively. Regarding (neo-)adjuvant anti-human epidermal growth factor-2 (HER2)-targeted therapy, the use of trastuzumab increased from 4.6% to 10.5%. The rate of sentinel lymph node biopsy increased from 37.1% to 60.7%, while that of axillary dissection decreased from 54.5% to 22.6%. Improvements in disease-free and overall survival were observed in patients with HER2-positive breast cancer, but there was no apparent trend in patients with hormone receptor-positive, HER2-negative, or triple-negative breast cancers.

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Data availability

Due to the nature of this research, participants of this study did not agree for their data to be shared publicly, so row data is not available.

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Acknowledgements

The authors thank all the affiliated institutes participating in the Breast Cancer Registry of the JBCS for their efforts to register the patients’ data.

Funding

This work was funded by the Registration Committee of the Japanese Breast Cancer Society.

Author information

Authors and Affiliations

Authors

Contributions

Study concept and design: TI, NN, YS and MM. Assembly of data: HK and NK. Manuscript writing: TI. Critical revision of the manuscript for important intellectual content: The Registration Committee of the JBCS (TI, NN, YS, MM, TK, NS, KT, MN, NH, MY, CW, and SS). Final approval of manuscript: All.

Corresponding author

Correspondence to Takayuki Iwamoto.

Ethics declarations

Conflict of interest

Grants or contracts from any entity: TI: Pfizer, NN: Chugai, Pfizer, Eisai, Mochida Institutional, Daiichi Sankyo and Novartis; TK: Pfizer Co. Ltd, Kanzawa Medical Research Foundation and Japan Kampo Medicines Manufacturers Association; MT: Chugai, Taiho, Takeda, JBCRG assoc., Pfizer, KBCRN assoc., Eisai, Eli-Lilly and companies, Daiichi-Sankyo, AstraZeneca, Astellas, Shimadzu, Yakult, Nippon Kayaku, AFI technology, Luxonus, Shionogi, GL Science, Sanwa Shurui, and Zene; SS: Taiho, Eisai, Chugai, Takeda, MSD, Astra Zeneca, and Daiichi Sankyo. Consulting fees: HK: EPS corporation; MY: Lilly Japan, and Roche Japan. Payment or honoraria for lectures: HK: Chugai Pharmaceuticals; NN: Chugai, Eli Lilly, MSD, Daiichi-Sankyo, AstraZeneca and Pfizer; YS: Pfizer, Astra Zeneca, Daiichi Sankyo, Eisai, Eli Lily, Chugai, MSD and Nihon Kayaku; MM: Chugai, AstraZeneca, Eli Lilly, Pfizer, MSD, Taiho, Daiichi Sankyo and Eisai; MN: Chugai, AstraZeneca, Eli Lilly, Pfizer, Novartis, Taiho, Daiichi Sankyo, Esai, Kyowa-Kirin, MSD, Myriad genetics and Denka; NH: Eli Lilly, Astrazeneca, taiho, Eizai, ExactScience,Daiichi-Sankyo, Novartis, Pfizer, and Chugai; MY: Agilent technologies, Chugai pharma, Ono Yakuhin, MSD, and Daiichi Sankyo; TM: Chugai, Takeda, Pfizer, Kyowa-Kirin, Taiho, Eisai, Daiichi-Sankyo, AstraZeneca, Eli Lilly and companies, Daiichi-Sankyo, MSD, Exact Science, Novartis, Shimadzu, Yakult, Nippon Kayaku, Devicore medical Japan, and Sysmex; SS: Chugai, Kyowa Kirin, MSD, Novartis, Eisai, Takeda, Daiichi Sankyo, Eli Lilly, Astra Zeneca, Pfizer, Taiho, Ono, and Nipponkayaku. Participation on a Data Safety Monitoring Board or Advisory Board: MT: Daiichi-Sankyo, Eli Lilly and companies, Bertis, Terumo, and Kansai Medical Ne; SS: Chugai/Roche, Astra Zeneca, Eli Lilly, Pfizer, Kyowa Kirin, Daiichi Sankyo, and MSD. Leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid: SS: JBCRG, JBCS, JSMO, and BIG.Other financial or non-financial interests: HK: Affiliation to HQA, a social collaborative department supported by National CLinlical Database, Johnson & Johnson KK, Nipro corporation and Intuitive Surgical Sarl; NK: Affiliation to HQA, a social collaborative department supported by National CLinlical Database, Johnson & Johnson KK, Nipro corporation and Intuitive Surgical Sarl; MT: British Journal of Cancer, Scientific Reports, Breast Cancer Research and Treatment, and Cancer Science.

Ethical approval

This study was approved by the Institutional Review Board (Permission number: 6200–00) at Kawasaki Medical School Hospital. This article does not contain any studies with animals performed by any of the authors. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Iwamoto, T., Kumamaru, H., Niikura, N. et al. Survival trends and patient characteristics between 2004 and 2016 for breast cancer in Japan based on the National Clinical Database-Breast Cancer Registry. Breast Cancer 31, 185–194 (2024). https://doi.org/10.1007/s12282-024-01545-x

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  • DOI: https://doi.org/10.1007/s12282-024-01545-x

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