Avoid common mistakes on your manuscript.
Research on breast cancer risk revealed that 5–10% of breast cancer patients are genetically predisposed to cancers [1]. More than 25 years have passed since BRCA1 was identified and cloned [2, 3]. BRCA 1 and BRCA 2 are well-known susceptibility genes for breast cancer, which are also associated with ovarian and pancreatic cancers. Recent advancement in the mechanism of hereditary breast cancer has changed the clinical approach to patients and families who are considered “high risk” for breast cancer. Genetic testing is becoming a feasible option to accurately estimate their own risk and to optimize screening/surveillance strategy.
Due to the accumulating evidence and continuous efforts by professional societies, several medical examinations, and treatments related to HBOC have become covered by insurance in Japan [4]. These include BRCA genetic testing to determine eligibility for PARP inhibitor therapy and for patients diagnosed with breast or ovarian cancers who are likely to have a genetic predisposition. For patients diagnosed as HBOC risk-reduced mastectomy (RRM), breast reconstruction, and risk-reduced oophorectomy (RRSO) are covered by insurance. MRI-guided biopsy was also covered by insurance.
Nowadays, clinicians and professionals who are involved in the management of breast cancer need to have sufficient knowledge of hereditary breast and ovarian cancer (HBOC) and other high-risk conditions of breast cancer to support patients’ choice. The benefit and harm of breast cancer screening/surveillance vary depending on individual risk of breast cancer. Conducting genetic testing and knowing the results affect patients’ life and families’ life and therefore fully-informed decisions should be made.
As a journal dedicated to breast cancer, we have dealt with the issues related to the high risk of breast cancer [5,6,7,8,9,10]. This special feature aims to cover important knowledge about HBOC that may be necessary in the clinic. Yoshida covers key factors for breast cancer genetics including BRCA 1 BRCA2 and other less-common risk genes [1]. The paper mentions the difference between western countries and Asian countries in frequencies of breast cancer-related genes, including higher prevalence of BRCA2 gene among Asian countries [11]. Since breast cancers associated with BRCA1 and 2 have different clinico-pathological features, their management may need to be adjusted for each group. Knowing other genes predisposing to cancer may be crucial for preventing future cancer in the breast and other organs. Genetic information varies depending on ethnicity, and we need to know the frequency of diseases and genes that are unique to us.
Screening strategy by imaging is a crucial component of HBOC management. The paper by Tozaki and Nakamura describes the current status of breast cancer screening in high-risk women in Japan [4]. Based on their prospective research project, they reported the data of image-based screening among Japanese women and the value of MRI surveillance. In addition, they claimed that different surveillance strategies should be used for BRCA 1 and 2 mutation carriers considering their different pattern of developing cancer with different imaging features. Triple-negative cancer is more common among BRCA1 mutation carriers and can appear benign like fibroademona, while the luminal-type breast cancer is more common in BRCA2 mutation carriers presenting calcification on mammogram in half of cases.
More practical side of MRI-guided vacuum-assisted biopsy (VAB) is covered in this featured paper [12]. There are a limited number of facilities which can regularly perform MRI-guided biopsy. However, MRI-guided VAB is the only method for MRI-only detected lesions often found on high-risk screening. In addition to the practical aspect, the data on MRI-guided- biopsy are nicely summarized.
Worldwide, various professional societies in many countries issue guidelines for breast cancer screening for normal and elevated risk of breast cancer. Onishi et al. encompass the guidelines and compare these guidelines [13]. There are variations in criteria among various groups/ country. These are useful guides for us to establish screening guidelines in our country.
I hope that these special feature papers are useful for reviewing up-to-date knowledge of HBOC for readers who are interested in this topic and are helpful in supporting those with high -risk of breast cancer.
References
Yoshida R. Hereditary breast and ovarian cancer (HBOC): review of its molecular characteristics, screening, treatment, and prognosis. Breast Cancer. 2020. https://doi.org/10.1007/s12282-020-01148-2. Epub ahead of print.
Miki Y, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994;266(5182):66–71.
Hall JM, et al. Linkage of early-onset familial breast cancer to chromosome 17q21. Science. 1990;250(4988):1684–9.
Tozaki M, Nakamura S. Current status of breast cancer screening in high-risk women in Japan. Breast Cancer. 2020. https://doi.org/10.1007/s12282-020-01103-1. Epub ahead of print.
Uematsu T et al. The Japanese Breast Cancer Society clinical practice guidelines for breast cancer screening and diagnosis, 2018 edition. Breast Cancer 2020; 27(1):17–24.
Tozaki M, et al. The Japanese Breast Cancer Society Clinical Practice Guideline for screening and imaging diagnosis of breast cancer. Breast Cancer. 2015;22(1):28–36.
Nakamura S, et al. Prevalence and differentiation of hereditary breast and ovarian cancers in Japan. Breast Cancer. 2015;22(5):462–8.
Okamoto S, et al. High-risk lesions diagnosed at MRI-guided vacuum-assisted breast biopsy: imaging characteristics, outcome of surgical excision or imaging follow-up. Breast Cancer. 2020;27(3):405–14.
Murakami W, et al. The clinical impact of MRI screening for BRCA mutation carriers: the first report in Japan. Breast Cancer. 2019;26(5):552–61.
Cipriano NM Jr, et al. Mutation screening of TP53, CHEK2 and BRCA genes in patients at high risk for hereditary breast and ovarian cancer (HBOC) in Brazil. Breast Cancer. 2019;26(3):397–405.
Momozawa Y, et al. Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls. Nat Commun. 2018;9(1):4083.
Takahama N, Tozaki M, Ohgiya Y. Current status of MRI-guided vacuum-assisted breast biopsy in Japan. Breast Cancer. 2020. https://doi.org/10.1007/s12282-020-01107-x. Epub ahead of print.
Onishi N, Kataoka M. Breast cancer screening for women at high risk: review of current guidelines from leading specialty societies. Breast Cancer. 2020. https://doi.org/10.1007/s12282-020-01157-1. Epub ahead of print.
Author information
Authors and Affiliations
Corresponding author
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
This article is published under an open access license. Please check the 'Copyright Information' section either on this page or in the PDF for details of this license and what re-use is permitted. If your intended use exceeds what is permitted by the license or if you are unable to locate the licence and re-use information, please contact the Rights and Permissions team.
About this article
Cite this article
Kataoka, M. Editorial: HBOC and high-risk screening: up-to-date. Breast Cancer 28, 1165–1166 (2021). https://doi.org/10.1007/s12282-021-01284-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12282-021-01284-3