Literature DB >> 27577200

[Knowledge and willingness of breast cancer patients from Shanghai for genetic counseling and gene testing].

Xiaolin Cheng1, Zhengdong Li, Xiaoyin Sun, Beiqi Jiang, Zhigang Zhuang.   

Abstract

OBJECTIVE: To investigate the knowledge and willingness of breast cancers patients from Shanghai for genetic counseling and gene testing.
METHODS: A total of 428 patients filled out the questionnaire and the data was statistically analyzed.
RESULTS: Most of the patients were unaware of genetic counseling and gene testing. But after a brief introduction, a majority of them were willing to accept genetic counseling and recommend their family members to participate. The willingness was education- and age-related. When told that gene testing may benefit themselves, 92.1% of the patients were willing to be tested. However, when told that gene testing may only benefit their family, only 33.9% of the patients were willing to join the testing. The acceptance was also age-, education- and family income-related. The difference was statistically significant. Moreover, the willingness ratio to participate the gene testing was lower than expected. Overall, 74.1% of the patients were willing to accept cheaper preliminary gene screening, whilst only 19.2% were willing to accept genetic testing of higher price. Despite of being told that testing results will be maintained as confidential, still 43.2% worried about adverse effects. Such patients tended to younger, from low-income families, with a family history of associated cancers, or personal history of other cancers. The difference was statistically significant.
CONCLUSION: The majorities of patients do not know but are willing to accept genetic counseling and gene testing and recommend their family to participate. Lack of genetic knowledge, cost for the testing and concerns about discrimination are the obstacles for patients to participate in genetic counseling and gene testing. To spread the knowledge about breast cancer and establish a follow-up screening system for high-risk population may improve the tertiary prevention for breast cancer.

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Year:  2016        PMID: 27577200     DOI: 10.3760/cma.j.issn.1003-9406.2016.05.001

Source DB:  PubMed          Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi        ISSN: 1003-9406


  3 in total

1.  Saliva samples as a source of DNA for high throughput genotyping: an acceptable and sufficient means in improvement of risk estimation throughout mammographic diagnostics.

Authors:  U G Poehls; C C Hack; A B Ekici; M W Beckmann; P A Fasching; M Ruebner; H Huebner
Journal:  Eur J Med Res       Date:  2018-04-27       Impact factor: 2.175

2.  Knowledge, Awareness, and Perception of Genetic Testing for Hereditary Disorders Among Malaysians in Klang Valley.

Authors:  Jia-Jia Chin; Hong-Wai Tham
Journal:  Front Genet       Date:  2020-12-03       Impact factor: 4.599

3.  Study on the differences of opinions and choices of high-risk breast cancer populations in China before and after genetic testing.

Authors:  Xiaolin Cheng; Zhangyuan Gu; Xiaoyin Sun; Zhigang Zhuang
Journal:  Transl Cancer Res       Date:  2019-12       Impact factor: 1.241

  3 in total

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