Masuda, Norikazu https://orcid.org/0000-0002-7302-0278
Yasojima, Hiroyuki https://orcid.org/0009-0005-3729-1520
Bando, Hiroko https://orcid.org/0000-0002-7361-3647
Yamanaka, Takashi https://orcid.org/0009-0004-0081-4263
Shigematsu, Hideo https://orcid.org/0000-0001-9393-9655
Takahashi, Masato https://orcid.org/0000-0002-6641-9598
Nagai, Shigenori E. https://orcid.org/0000-0003-2887-6066
Ito, Mitsuya
Aruga, Tomoyuki https://orcid.org/0000-0003-3442-8972
Tokiwa, Mariko https://orcid.org/0000-0003-4405-8231
Imoto, Shigeru https://orcid.org/0000-0002-0878-7851
Nakamura, Rikiya https://orcid.org/0000-0002-4349-9046
Ishiguro, Hiroshi https://orcid.org/0000-0002-9859-5932
Kawabata, Hidetaka https://orcid.org/0000-0002-4321-9067
Saji, Shigehira https://orcid.org/0000-0002-6732-8030
Haga, Hironori https://orcid.org/0000-0003-4322-9561
Morita, Satoshi https://orcid.org/0000-0002-4344-3317
Toi, Masakazu https://orcid.org/0000-0003-1488-9958
Clinical trials referenced in this document:
Documents that mention this clinical trial
Eribulin-based neoadjuvant chemotherapy for triple-negative breast cancer patients stratified by homologous recombination deficiency status: a multicenter randomized phase II clinical trial
https://doi.org/10.1007/s10549-021-06184-w
Long-term outcomes of eribulin‑based neoadjuvant chemotherapy for triple‑negative breast cancer patients stratified by homologous recombination deficiency status: results of the randomized JBCRG-22 study
https://doi.org/10.1007/s10549-026-07917-5
Funding for this research was provided by:
Japan Breast Cancer Research Group (JBCRG) and Eisai Co., Ltd.
Article History
Received: 12 September 2025
Accepted: 2 February 2026
First Online: 19 March 2026
Declarations
:
: Authors received support from Eisai for medical writing and the article processing charge for the submitted article. NM declared receiving grants/contracts (institution) from Chugai Pharmaceutical, Eli Lilly, AstraZeneca, Pfizer, Daiichi Sankyo, MSD, Eisai, Novartis, Gilead Sciences and Ono Pharmaceutical; honoraria (personal) from Chugai Pharmaceutical, Pfizer, AstraZeneca, Eli Lilly, Daiichi Sankyo, Eisai, Gilead Sciences and MSD; and serving as a representative of the Board of Directors (unpaid, 2021–2025) and as a member of the Board of Directors (unpaid, 2007–present) of Japan Breast Cancer Research Group (JBCRG), as a member of the Board of Directors (unpaid, 2021–2024) of Japanese Breast Cancer Society (JBCS), as a member of the Board of Directors (unpaid, 2023–present) of Japan Society of Clinical Oncology (JSCO), and as a member of the Board of Directors (unpaid, 2024–present) of Japan Association of Breast Cancer Screening (JABCS), and as a representative of the Board of Directors (unpaid, 2025–present) of Kyoto Breast Cancer Research Network (KBCRN). HB declared receiving honoraria for lectures (personal) from Chugai Pharmaceutical, Daiichi Sankyo, Eli Lilly, Eisai, Kyowa Kirin, AstraZeneca, Pfizer and MSD. TY declared receiving consulting fees (personal) from Daiichi Sankyo, Eli Lilly, and Pfizer; honoraria (personal) from AstraZeneca, Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Eli Lilly, Gilead Sciences, Kyowa Kirin, Pfizer, and Taiho Pharmaceutical. HS declared receiving honoraria (personal) from Daiichi Sankyo, Chugai Pharmaceutical, Eli Lilly, Taiho Pharmaceutical, MSD, Eisai, Kyowa Kirin, Pfizer, and AstraZeneca. M (Takahashi) declared receiving honoraria for lectures (personal) from AstraZeneca, Eli Lilly, Daiichi Sankyo, MSD, Eisai, and Pfizer. SEN declared receiving honoraria (personal) from Pfizer, Eli Lilly, MSD, Chugai Pharmaceutical, Gilead Sciences, AstraZeneca, Daiichi Sankyo, and Eisai. TA declared receiving grants/contracts (personal) from Pfizer; honoraria (personal) from Pfizer, Chugai Pharmaceutical, AstraZeneca, Eli Lilly, Kyowa Kirin, MSD, and Daiichi Sankyo; receipt of equipment, materials, drugs, medical writing support, gifts, or other services from AstraZeneca, Mochida Pharmaceutical, and Pfizer. M (Tokiwa) declared receiving honoraria (personal) from Daiichi Sankyo. RN declared receiving honoraria (personal) from Chugai Pharmaceutical, Daiichi Sankyo, Eli Lilly, Medicone BD, AstraZeneca, Nippon Kayaku, Exact Sciences, and Kyowa Kirin. HI declared receiving grants/contracts (institution) from Eisai, Daiichi Sankyo, Chugai Pharmaceutical, Takeda Pharmaceutical, AstraZeneca, MSD, Ono Pharmaceutical, and Nipro; consulting fees (personal) from Mitsubishi Tanabe, AstraZeneca, and Asahi Kasei; honoraria (personal) from Eisai, Chugai Pharmaceutical, Pfizer, Kyowa Kirin, Daiichi Sankyo, Taiho Pharmaceutical, AstraZeneca, MSD, and Eli Lilly. SS declared receiving grants/contracts (institution) from Taiho Pharmaceutical, Eisai, Chugai Pharmaceutical, Takeda Pharmaceutical, MSD, AstraZeneca, Daiichi Sankyo, Gilead Sciences, Eli Lilly, and Sanofi; honoraria (personal) from Chugai Pharmaceutical, Kyowa Kirin, MSD, Novartis, Eisai, Takeda Pharmaceutical, Daiichi Sankyo, Eli Lilly, AstraZeneca, Pfizer, Taiho Pharmaceutical, Ono Pharmaceutical, Nippon Kayaku, Gilead Sciences, and Exact Sciences; participation on a Data Safety Monitoring Board or Advisory Board for Chugai/Roche, AstraZeneca, Eli Lilly, Pfizer, Kyowa Kirin, Daiichi Sankyo, and MSD; serving as an executive board member of JBCRG, JBCS, and Japanese Society of Medical Oncology (JSMO). SM declared receiving honoraria (personal) from AstraZeneca, Bristol Myers Squibb, Chugai Pharmaceutical, Eli Lilly, MSD, and Ono Pharmaceutical. M (Toi) declared receiving grants (institution) from Kansai Med Net, AFI technology, Eisai, Astellas, Nippon Kayaku, Taiho Pharmaceutical, Sanwa Syurui, Shimadzu, Chugai Pharmaceutical, Pfizer, Yakult, Zene, AstraZeneca, JBCRG, and Eisai; consulting fees (personal) from Bertis, Eli Lilly, and Daiichi Sankyo; honoraria (personal) from AstraZeneca, MSD, Eisai, Devicor Medical Japan, Kyowa Kirin, Daiichi Sankyo, Eli Lilly, Nippon Kayaku, Taiho Pharmaceutical, Exact Sciences, Shimadzu, Chugai Pharmaceutical, Pfizer, Yakult, and Sysmex; serving as a chairman (unpaid) for JBCS and a member of the Board of Directors of JBCRG and KBCRN; as an associate editor for Breast Cancer Research and Treatment, Science Reports and Cancer Science. HY, MI, SI, HK, and HH declared no conflicts of interest related to the work.
: The study was conducted in accordance with the Declaration of Helsinki and the Ethical Guidelines for Clinical Research of the Ministry of Health, Labour and Welfare of Japan. The study protocol was reviewed and approved by the institutional review board of each participating institution upon study initiation.
: All patients provided informed consent to participate in the JBCRG-22 study. Additional consent for data to be collected from their medical records and included in the present analysis was considered unnecessary, because no further interventions were involved.
: Not applicable.