Sharing genetic test results of germline pathogenic variants of hereditary cancer with relatives: A single-center cross-sectional study. (8th July 2021)
- Record Type:
- Journal Article
- Title:
- Sharing genetic test results of germline pathogenic variants of hereditary cancer with relatives: A single-center cross-sectional study. (8th July 2021)
- Main Title:
- Sharing genetic test results of germline pathogenic variants of hereditary cancer with relatives: A single-center cross-sectional study
- Authors:
- Fukuzaki, Naomi
Kiyozumi, Yoshimi
Higashigawa, Satomi
Horiuchi, Yasue
Mizuguchi, Maki
Matsubayashi, Hiroyuki
Nishimura, Seiichiro
Mori, Keita
Notsu, Akifumi
Suishu, Izumi
Ohnami, Sumiko
Kusuhara, Masatoshi
Yamaguchi, Ken
Doorenbos, Ardith Z
Takeda, Yuko - Abstract:
- Abstract: Objective: This study aimed to determine whether Japanese cancer patients share test results of germline pathogenic variants of hereditary cancer with their relatives. Methods: This single-center cross-sectional study enrolled 21 Japanese patients who received results of germline pathogenic variants of hereditary cancer at least 6 months prior. Results: All patients shared their test results with at least one relative, with the following sharing rates: 85.7% for first-degree relatives, 10% for second-degree relatives and 8.3% for third-degree relatives. Patients most commonly shared the information with their children aged >18 years (86.7%), followed by their siblings (73.6%), spouses (64.7%) and parents (54.5%). Three categories were extracted from qualitative analysis: 'characteristics of my cancer', 'knowledge and caution about inheritability' and 'utilization of medical care.' Conclusions: The rate of test result sharing with first-degree relatives was comparable with those in Europe and the USA. Patients with germline pathogenic variants also tended to share their test results more with their children and siblings than with their parents. Informing their relatives of the results was suggestive of the motivation to influence their relatives' health outcome and contribute to the well-being of their children and siblings. Abstract : Japanese patients with germline pathogenic variants of hereditary cancers disclosed their test results to at least one relative,Abstract: Objective: This study aimed to determine whether Japanese cancer patients share test results of germline pathogenic variants of hereditary cancer with their relatives. Methods: This single-center cross-sectional study enrolled 21 Japanese patients who received results of germline pathogenic variants of hereditary cancer at least 6 months prior. Results: All patients shared their test results with at least one relative, with the following sharing rates: 85.7% for first-degree relatives, 10% for second-degree relatives and 8.3% for third-degree relatives. Patients most commonly shared the information with their children aged >18 years (86.7%), followed by their siblings (73.6%), spouses (64.7%) and parents (54.5%). Three categories were extracted from qualitative analysis: 'characteristics of my cancer', 'knowledge and caution about inheritability' and 'utilization of medical care.' Conclusions: The rate of test result sharing with first-degree relatives was comparable with those in Europe and the USA. Patients with germline pathogenic variants also tended to share their test results more with their children and siblings than with their parents. Informing their relatives of the results was suggestive of the motivation to influence their relatives' health outcome and contribute to the well-being of their children and siblings. Abstract : Japanese patients with germline pathogenic variants of hereditary cancers disclosed their test results to at least one relative, mostly first-degree relatives, including the patients' adult children, siblings, spouses and parents. … (more)
- Is Part Of:
- Japanese journal of clinical oncology. Volume 51:Number 10(2021)
- Journal:
- Japanese journal of clinical oncology
- Issue:
- Volume 51:Number 10(2021)
- Issue Display:
- Volume 51, Issue 10 (2021)
- Year:
- 2021
- Volume:
- 51
- Issue:
- 10
- Issue Sort Value:
- 2021-0051-0010-0000
- Page Start:
- 1547
- Page End:
- 1553
- Publication Date:
- 2021-07-08
- Subjects:
- family -- genetic testing -- germ-line mutation -- hereditary -- neoplastic syndromes
Oncology -- Periodicals
Cancer -- Periodicals
616.994005 - Journal URLs:
- http://jjco.oupjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/jjco/hyab110 ↗
- Languages:
- English
- ISSNs:
- 0368-2811
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4651.378000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19125.xml