Literature DB >> 26025266

Willingness of Japanese patients with breast cancer to have genetic testing of BRCA without burden of expenses.

Hiroshi Nakagomi1,2, Ikuko Sakamoto3, Yosuke Hirotsu4, Kenji Amemiya4, Hitoshi Mochizuki4, Masayuki Inoue5, Satoko Nakagomi6, Takeo Kubota7, Masao Omata4,8.   

Abstract

BACKGROUND: Genetic analysis for individuals who are at risk for hereditary breast and ovarian cancer syndrome (HBOC) has becoming widely accepted. The poor introduction of the genetic testing of BRCA in Japan compared with western countries could be due to insufficient recognition of its importance, prejudice against a heredity disease, especially in non-urban districts, and its high cost. There is few available data regarding the acceptance or willingness to have genetic testing among Japanese who are at risk and living outside Tokyo.
METHODS: Of 670 patients seen and detailed family history taken at our hospital, located non-urban, 30 (4 %) gave the family history of breast cancer in more than 2 members within the second degree relatives ("stronger" family history group), 92 (14 %) in 1 member ("weaker" group), and 548 (82 %) in none of members ("sporadic" group). Then, we selected 107 (24 from "stronger", 50 from "weaker", 33 from "sporadic" family history group) to see if they are willing to receive cost-free genetic testing of BRCA 1 and BRCA2.
RESULTS: Ninety-two of 107 (86 %) patients agreed and 15 (14 %) refused. The rate of refusal for BRCA testing was higher in "stronger family history group" (6/24, 25 %) compared to "weaker" (7/50, 14 %) or "sporadic" (2/33, 6 %) (p = 0.04), respectively.
CONCLUSIONS: These data indicate that the currently available preventive measures and/or counseling system may not be sufficient enough to convince the high risk population to receive the genetic testing or to overcome the prejudice in non-urban area in Japan, even if served free.

Entities:  

Keywords:  BRCA; Breast cancer; Family history; Ovarian cancer

Mesh:

Substances:

Year:  2015        PMID: 26025266     DOI: 10.1007/s12282-015-0618-7

Source DB:  PubMed          Journal:  Breast Cancer        ISSN: 1340-6868            Impact factor:   4.239


  4 in total

1.  Baseline knowledge and receptiveness to genetic testing for hereditary breast and ovarian cancer syndromes in Chinese high-risk females.

Authors:  Annie Tsz-Wai Chu; Desiree Man-Sik Tse; Dacita To Ki Suen; Ava Kwong
Journal:  J Community Genet       Date:  2021-04-30

2.  Analysis of significantly mutated genes as a clinical tool for the diagnosis in a case of lung cancer.

Authors:  Yoshihiro Miyashita; Yosuke Hirotsu; Toshiharu Tsutsui; Seishi Higashi; Yusuke Sogami; Yumiko Kakizaki; Taichiro Goto; Kenji Amemiya; Toshio Oyama; Masao Omata
Journal:  Respir Med Case Rep       Date:  2017-02-17

3.  Investigating men's motivations to engage in genetic screening for BRCA1 and BRCA2 mutations.

Authors:  Anna Maria Annoni; Claudia Longhini
Journal:  PLoS One       Date:  2022-03-18       Impact factor: 3.240

4.  Simultaneous detection of genetic and copy number alterations in BRCA1/2 genes.

Authors:  Yosuke Hirotsu; Yoshihiko Ooka; Ikuko Sakamoto; Hiroshi Nakagomi; Masao Omata
Journal:  Oncotarget       Date:  2017-12-06
  4 in total

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